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Article

Matching between Donors and Ulcerative Colitis Patients Is Important for Long-Term Maintenance after Fecal Microbiota Transplantation

Department of Gastroenterology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2020, 9(6), 1650; https://doi.org/10.3390/jcm9061650
Submission received: 28 April 2020 / Revised: 27 May 2020 / Accepted: 28 May 2020 / Published: 31 May 2020

Abstract

:
We previously demonstrated that fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, metronidazole (AFM); A-FMT) resulted in effective colonization of Bacteroidetes species, leading to short-term clinical response in ulcerative colitis (UC). Its long-term efficacy and criteria for donor selection are unknown. Here, we analyzed the long-term efficacy of A-FMT compared to AFM monotherapy (mono-AFM). AFM was administered to patients with mild to severe UC for 2 weeks until 2 days before fresh FMT. Clinical response and efficacy maintenance were defined by the decrease and no exacerbation in clinical activity index. The population for intention-to-treat analysis comprised 92 patients (A-FMT, n = 55; mono-AFM, n = 37). Clinical response was observed at 4 weeks post-treatment (A-FMT, 56.3%; mono-AFM, 48.6%). Maintenance rate of responders at 24 months post-treatment was significantly higher with A-FMT than mono-AFM (p = 0.034). Significant differences in maintenance rate according to the age difference between donors and patients were observed. Additionally, sibling FMT had a significantly higher maintenance rate than parent–child FMT. Microbial analysis of patients who achieved long-term maintenance showed that some exhibited similarity to their donors, particularly Bacteroidetes species. Thus, A-FMT exhibited long-term efficacy. Therefore, matching between donors and UC patients may be helpful in effectively planning the FMT regimen.

1. Introduction

Recent studies have suggested that microbiota is associated with not only digestive diseases but also several other diseases (e.g., liver disease, cardiovascular disease, obesity, allergies, diabetes, mental disorders) [1,2,3,4,5]. Fecal microbiota transplantation (FMT) has been proposed as a microbial therapy for a wide range of other dysbiosis-related diseases such as metabolic syndrome [6], irritable bowel syndrome [2], autism spectrum disorder [7], and inflammatory bowel disease (IBD), considering that the usefulness of FMT for Clostridioides difficile infection (CDI) was reported by Van Nood [8,9]. Ulcerative colitis (UC) is considered to be intricately attributable to numerous factors, including genetic [10], immunological, and environmental factors [11], and microbiota is one of these [12,13,14]. Some randomized controlled trials targeting UC have been reported from 2015 to 2019 [15,16,17,18]. Three reports have described the efficacy of FMT, administered multiple times, in UC patients [15,16,17]. Although the efficacy of FMT as a short-term treatment for UC has been recognized, the method employed is too cumbersome to be put into practical use. To our knowledge, few studies have examined the therapeutic efficacy of FMT as a long-term treatment for UC [19]. Additionally, several studies have employed volunteer donors, and there is no consensus on the selection of appropriate donors [20]. Increasing the diversity of microbiota is important for inducing remission [21] and matching between donors and recipients may be important when considering stabilized microbiota for prevention of recurrence [22]. Therefore, long-term evaluation of FMT is indispensable and may lead to the formulation of criteria for the selection of appropriate donors. In the present study, our method called A-FMT (FMT following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole; AFM)) is simple to use in clinical practice because it entails FMT via colonoscopy once after antibiotic administration for 2 weeks. We had previously reported that a single session of A-FMT efficiently changed the gut microbiota and the change in Bacteroidetes species was associated with the short-term efficacy of the treatment [23,24]. It was proven that patients who showed a therapeutic effect had their gut microbiota successfully transplanted by the donors. In the present study, we analyzed the long-term efficacy of A-FMT compared to AFM monotherapy (mono-AFM) and explored the criteria for a beneficial donor for long-term maintenance (24 months) after A-FMT.

2. Materials and Methods

2.1. Ethical Considerations

The study protocol was reviewed and approved by the ethics committee of the Juntendo Institutional Review Board at the Juntendo University School of Medicine and the clinical study committee of Juntendo University Hospital (approval numbers 14-017, 15-059, and 16-201). Furthermore, this trial has been registered at http://www.umin.ac.jp/ctr/index-j.htm:UMIN000014152, http://www.umin.ac.jp/ctr/index-j.htm:UMIN000018642, and http://www.umin.ac.jp/ctr/index-j.htm:UMIN000025846. All participants provided written informed consent. All studies were performed at Juntendo University Hospital (Tokyo, Japan).

2.2. Patient and Public Involvement

This research was conducted without patient involvement. Patients were not invited to comment on the study design or to contribute to the writing or editing of the article for readability or accuracy and were not consulted to develop relevant patient outcomes or interpret the results.

2.3. Patients

A non-randomized controlled study was conducted between July 2014 and March 2017 at Juntendo University Hospital (Tokyo, Japan). The diagnosis of UC was based on standard clinical, endoscopic, and histological findings [25]. The inclusion criteria for this study were as follows: age ≥20 years, diagnosis of active UC with a Lichtiger’s clinical activity index (CAI) score ≥5, or Mayo endoscopic score ≥1. This study included patients with UC who did not achieve clinical remission because of refraction to adequate treatment, including 5-aminosalicylates (5-ASA), immunomodulators, corticosteroids, and/or biologics. In addition, patients with allergies and/or side effects to 5-ASA and biologics were also included, even if their UC was mild. A total of 92 patients were enrolled in this study. Of these patients, 37 were treated with mono-AFM and included in the control group. Meanwhile, 55 patients were treated with A-FMT. The patients chose the mono-AFM or A-FMT regimen by themselves. The patients who could not find an appropriate donor candidate chose the mono-AFM regimen. Additionally, some patients chose mono-AFM owing to its convenience and its proven efficacy.
The exclusion criteria were the presence of cytomegalovirus colitis, current serious disease, pregnancy, participation in other clinical studies, or antibiotic use within 3 months prior to participation in this study.

2.4. Donors

Spouses and relatives were selected as donors by the patients. Donors needed to be ≥20 years old and in good health. Donor candidates provided information regarding their medical history, current diseases, travel history, sexual behavior, recent gastrointestinal tract infections, and defecation habits.
Donor candidates who had used antibiotics within 3 months before participating in the study were not included. The stool and blood samples of the donors were collected at the time of their visit to the hospital. Blood and feces samples of donors were checked using the Amsterdam Protocol [26,27,28]. The donors with the serologic presence of hepatitis B and C viruses, human immunodeficiency virus, cytomegalovirus, and syphilis were excluded from the study. The feces samples were tested for the presence of Clostridioides difficile, enterohemorrhagic Escherichia coli, Salmonella, Shigella, Yersinia, Campylobacter, parasites, and helminths. If this screening test was positive, the donor candidate was excluded from the study.

2.5. Protocol for AFM Monotherapy

Patients received a combination antibiotic regimen consisting of oral amoxicillin (1500 mg/day), fosfomycin (3000 mg/day), and metronidazole (750 mg/day) for 2 weeks. After AFM monotherapy, the patients were permitted to continue the ongoing treatment and were regulated in terms of probiotic intake during the study period. Change in drug dosage or the initiation of new treatment was not allowed.

2.6. Protocol for A-FMT

We have already reported the method of A-FMT therapy [23,24]. Briefly, the patients received AFM therapy for 2 weeks until 2 days before undergoing fresh FMT. We placed 300–500 mL of the extracted suspension containing the donor’s microbiota in 20 mL syringes. After bowel lavage using a standard polyethylene glycol solution (Moviprep; EA Pharma, Tokyo, Japan), the patients underwent total colonoscopy. Then, 350–500 mL of the diluted and filtered bacterial suspensions were transferred into the patient’s colon, preferably within 6 h after collecting stool samples. About two-thirds of the bacterial suspension was injected into the cecum and ascending colon, and the remaining portion was injected into the transverse colon. After the procedure, scopolamine was administered to patients to slow the intestinal transit and allow sufficient time for the colonization of donor bacteria; following which, the patients had the same restrictions as those in the mono-AFM group.

2.7. Clinical Evaluation

For short-term estimation, the clinical features of UC were evaluated using the CAI score before treatment, after antibiotic combination therapy, and at 4 weeks after treatment. After 4 weeks of treatment, clinical response was defined as a CAI score of ≤10 points and a decrease of ≥3 points. Meanwhile, remission was defined as a CAI score of ≤3 points. Disease activity was evaluated at the time of colonoscopy. In the A-FMT group, colonoscopy was conducted at the time of FMT following the AFM administration. The clinical features were observed at 4 weeks after the FMT. In the mono-AFM group, the colonoscopy was performed after AFM administration and clinical features were observed at 4 weeks after the AFM. The endoscopic assessment was performed using the Mayo endoscopic score, particularly the sum of Mayo endoscopic scores [29], which included seven segments of the large intestine (appendicular region, cecum, ascending colon, transverse colon, descending colon, sigmoid colon, and rectum), to determine the overall disease status of patients with UC. For the long-term evaluation of short-term responders, clinical score evaluation was performed at the time of outpatient visit every 1–2 months. Patients who could not visit our hospital as outpatients were regularly interviewed via telephone and mail every 3–6 months. Subsequently, it was confirmed whether their symptoms were exacerbated (estimated by CAI) and/or whether a new treatment was initiated. Patients exhibiting exacerbation of symptoms and/or intensification of treatment, which included an increase in dosage or switching to a new treatment, were defined as being in relapse.

2.8. Microbial Analysis

In this study, we used universal hsp60 primers without adapter sequences. We have already reported the method for microbial analysis involving DNA extraction, amplification by a polymerase chain reaction, preparation of DNA libraries for next-generation sequencing, quality filtering of sequencing reads, and taxonomic analysis based on Bacteroidetes HSP60 sequences [24]. Fecal samples for microbial analysis were collected from 5 out of 10 patients who remained to demonstrate no recurrence for 24 months after undergoing A-FMT and from individual FMT donors. The feces from individual patients and donors were diluted 10-fold in TE buffer (10 mM Tris, 1 mM EDTA (pH 8.0]) and were frozen at −80 °C until use. We observed the relationship of gut microbiota between the patients who had treatment effects and their donors using HSP60 sequences. We analyzed bacterial species with ≥0.1% presence in the donors and post-treatment patients and excluded the unclassified bacterial species.

2.9. Statistical Analysis

The results of the clinical efficacy were evaluated by intention-to-treat (ITT) analysis. Differences in the event-free survival rate between the mono-AFM and A-FMT groups were estimated using the Gehan–Breslow–Wilcoxon test and log-rank test. Analysis of factors between donors and patients in A-FMT was conducted using the log-rank test. Differences with P values ≤0.05 were considered statistically significant. Chi-square test was used to compare clinical response and clinical remission between the groups. Similarities between Bacteroidetes species in stool samples were calculated using Morisita’s Cλ and Kimoto’s Cπ values, and a dendrogram was constructed from Horn’s R0 values [30,31,32].

2.10. Data Availability Statement

All data generated or analyzed during this study are included in this published article and its supplementary information files.

3. Results

3.1. Adverse Events

Among 92 patients treated with AFM, 12 patients (13.0%) showed the exacerbation of diarrhea, rash, and nausea due to antibiotics. However, after the end of the AFM regimen or withdrawal from oral administration (drop-out from the study), all symptoms improved, and no serious drug-related toxicities were observed. Adverse events due to FMT included exacerbation of nausea and prokinetic bowel peristalsis, which were observed in 20 patients (42.6%). Nevertheless, both were transient, and no serious infection or diarrhea was observed.

3.2. Short-Term Clinical Evaluation

A total of 92 patients were enrolled in this study between July 2014 and March 2017. Of these patients, 37 were assigned to the mono-AFM group, and 55 were allocated to the A-FMT group. Among 37 patients in the mono-AFM group, five withdrew without waiting for treatment evaluation after 4 weeks because of the adverse effects of antibiotics, exacerbation of other diseases, improvement in symptoms before AFM administration, and no hospital visit. Among 55 patients in the A-FMT group, eight withdrew because of the adverse effects of antibiotics, exacerbation of UC, physician’s decision, and no hospital visit. The clinical characteristics of these 92 patients are summarized in Table 1. The ratio of males to females was significantly higher in the A-FMT group than in the mono-AFM group.
The clinical efficacy of treatment regimens for UC was evaluated using ITT analysis and estimated using the CAI score after 4 weeks of treatment. In the A-FMT group, 31 patients (56.3%) showed a clinical response and 19 patients (34.5%) achieved clinical remission. These rates were higher than the rates observed in the mono-AFM group (clinical response/remission: n = 18/6, 48.6%/16.2%) (Figure 1).
The sum of Mayo endoscopic scores of responders in the A-FMT group was significantly lower than that of non-responders (responders: n = 31, 5.0 ± 3.6; non-responders: n = 16, 7.6 ± 3.1; p = 0.02). In contrast, this tendency was not observed in the mono-AFM group (responders: n = 18, 6.8 ± 4.1; non-responders: n = 14, 5.7 ± 4.5; p = 0.47) (Figure S1). Comparison of disease distribution revealed that the response and remission rates in the A-FMT group were significantly higher among patients with proctitis than among patients with left-sided and extensive colitis (left-sided and extensive colitis, n = 46; proctitis, n = 9; clinical response, p = 0.06; clinical remission, p = 0.005). No significant differences in the extent of disease were observed in the mono-AFM group (left-sided and extensive colitis, n = 33; proctitis, n = 4; clinical response, p = 1; clinical remission, p = 0.52) (Figure 2).
Comparing the efficacy of A-FMT in patients according to ongoing and past medication use, we found that the decrease in the CAI score was significantly lower in users of anti-tumor necrosis factor-α and corticosteroids than in non-users (p = 0.03, p = 0.009, respectively) (Figure S2). No significant differences in other treatments were observed for the decrease in CAI score. Additionally, no significant difference was observed in the correlation between donor matching and efficacy.

3.3. Long-Term Clinical Evaluation

In the A-FMT group, 13 patients (23.6%; ITT analysis) did not experience relapse within 12 months, and 10 (18.2%) patients did not experience relapse within 24 months after undergoing A-FMT. Meanwhile, in the mono-AFM group, six patients (16.2%) did not experience relapse within 12 months, and four patients (10.8%) did not experience relapse within 24 months after AFM administration. Long-term evaluation between two groups was conducted on patients in whom a therapeutic effect was observed at 4 weeks after treatment. One patient in the A-FMT group was excluded because of dysplasia detected by biopsy at the time of FMT; wherein, his clinical symptoms had improved. Therefore, the long-term course was examined in 30 patients belonging to the A-FMT group (Table 2) and 18 patients belonging to the mono-AFM group (Figure 3).
Patients exhibiting exacerbation of symptoms, which led to an increase in the CAI score by ≥1 point, and/or intensification of treatment were defined as being in relapse. The cumulative non-relapse rate after 24 months was significantly higher in the A-FMT group than in the mono-AFM group (p = 0.034, Wilcoxon test; Figure 4).
Further, we examined the relationship between factors related to therapeutic effects and donors in the A-FMT group. We divided the patients into two groups according to the age difference between the donor and the patient—namely, the 0–10-year difference group (n = 16) and the ≥11-year difference group (n = 14)—and subsequently conducted a long-term evaluation. The cumulative non-relapse rate was significantly lower in the ≥11-year difference group than in the 0–10-year difference group (p = 0.003, log-rank test; Figure 5a). Until now, the elderly donors were considered to be unsuitable for FMT. However, the FMT employing elderly donors proved to be effective in our study (Table 2, cases #4, #25, and #26). We also divided the patients into the following three groups based on the relationship with the donor: sibling FMT (n = 7), parent-child or child-parent FMT (n = 13), and other FMT (n = 10, including spouse and cousin). We observed that sibling FMT had a significantly higher cumulative non-relapse rate than parent-child FMT (p = 0.007, log-rank test; Figure 5b).

3.4. Microbial Analysis for Long-Term Study

Bacteroidetes species that existed in donors continued to exist in five patients who remained to demonstrate no recurrence for 24 months (Table 3).
Bacteroides uniformis and Parabacteroides distasonis were found in all five cases, and Bacteroides dorei was found in 4 out of 5 cases. We showed the change in the composition of Bacteroidetes species between the Bacteroidetes species in 10 samples (donor, patient before A-FMT, at 2 weeks and 1, 2, 3, 5, 6, 12, and 24 months after A-FMT) for case #11 (Figure 6a). Ten Bacteroidetes species existed for 24 months (Table 3) and were more similar to the donor than to the recipient’s bacterial composition before the therapy. The patient was in remission (both clinical and endoscopic) for 24 months after receiving a single A-FMT regimen (Figure 6b). These results suggest that there was an improvement in microbiota colonized from a healthy donor, along with clinical improvement after undergoing A-FMT. However, such a clear tendency was not confirmed in other cases (Table S1).
(1)
Baseline endoscopic appearance of the descending colon with active colitis; clinical activity index (CAI) score = 14, endoscopic subscore = 3.
(2)
Endoscopic appearance at the end of 1 month after A-FMT; CAI score = 4, endoscopic subscore = 1.
(3)
Endoscopic appearance at the end of 6 months after A-FMT; CAI score = 1, endoscopic subscore = 1.
(4)
Endoscopic appearance at the end of 24 months after A-FMT; CAI score = 1, endoscopic subscore = 1.
The patient remained in clinical remission at the final follow-up of the study (i.e., 24 months after A-FMT).

4. Discussion

During the short-term evaluation, the response and remission rates in the present study were observed to be significantly higher in patients with proctitis than in patients with other types of colitis in the A-FMT group. However, this tendency was not observed in the mono-AFM group. We had previously reported that the A-FMT regimen synergistically contributed to the recovery of Bacteroidetes composition associated with clinical response and endoscopic severity (endoscopic sum score) [23,24]. The findings of the present study strengthen our previous results. These findings suggest that microbiota transplantation will not be successful if the patient’s intestinal tract does not have sufficient mucins for bacterial colonization because Bacteroidetes species may be unable to adhere to the niche of the extensively damaged mucosa, which might have lost essential components related to intestinal immunity [33]. Moreover, it has been reported that intestinal IgA in the mucin layer is important for the control of commensal gut microbiota and that the selective action of intestinal bacteria by IgA may be related to the mechanism of bacterial colonization [34].
Further, regarding the long-term clinical evaluation of A-FMT, to the best of our knowledge, this is a valuable report to highlight the importance of donor selection for FMT in UC. In the present study, the noteworthy observations related to the microbiota are as follows: (1) cumulative non-relapse rate in the long-term was significantly higher in the A-FMT group than in the mono-AFM group; and (2) matching between donors (e.g., siblings, close in age) and patients is an essential factor for long-term maintenance. However, this trend was not observed during short-term evaluation. Previously, we have reported that eradication of indigenous bacterial microbiota by AFM pre-treatment may promote the effective colonization of Bacteroidetes species supplied by FMT [23,24]. AFM therapy may enhance the long-term maintenance of FMT by eradicating pathogenic bacteria and resetting the dysbiotic intestinal microbiota while minimizing the recipient microbiota, thereby facilitating the establishment of exogenous microbiota. FMT may also reverse antimicrobial-associated dysbiosis caused by AFM therapy, thereby enhancing the efficacy of the treatment. Recent studies have demonstrated that the choice of the donor does not influence the clinical efficacy of FMT in comprising CDI patients [35,36]. On the contrary, the microbial diversity of donors is a major factor influencing the efficacy of FMT in UC patients [12,37]. Two reasons may explain this difference from our findings. One plausible reason for this difference is the criteria for donor selection. Most studies on FMT have employed non-relatives as donors for convenience of delivery to many patients, whereas we recruited the patients’ relatives as donors. This approach for donor selection can reveal the importance of matching between donors and recipients. Another possible reason for the difference is the administration of multiple antibiotics during the pre-treatment period. The traditional method for repeated FMT (intensive FMT) is a way to induce therapeutic effects by raising diversity and operational taxonomic units. In A-FMT, AFM antibiotic pre-treatment resets its microbiota, and matching of microbiota is important for whole microbiota transplantation [9,38]. Therefore, using a single donor is more reasonable than employing multiple donors in A-FMT.
It is interesting to note that the short-term efficacy of A-FMT is not associated with the type of donors and that donor selection can affect long-term maintenance and prevent relapse in A-FMT. “Colonization” of microbiota may be different from its “stabilization” such that the long-term maintenance rate is affected in UC. In other words, colonization is not associated with the type of donors, whereas stabilization of microbiota depends on the donors. Genetic and immunologic factors may influence the stabilization of microbiota. Related healthy individuals are known to harbor similar gut microbiota [39]. Some studies have reported that the acquisition of gut microbiota predominantly occurs over the first few years of life because the epidemiological associations of IBD are linked to the early childhood stage (including delivery, breastfeeding, weaning diet, maternal inoculum, and home environment) and subsequent antibiotic exposures [40,41,42]. The gut microbiota of siblings may reflect microbiota prior to UC development in patients, although we employed relatives as donors with a risk for developing UC because genetic susceptibility is also an important factor for IBD. Furthermore, the results of our study suggest that donors with less difference in age had acceptable microbiota to the patients. Of note, in cases #4, #25, and #26, the elderly patients received feces from elderly donors. Nevertheless, some reports have suggested that the loss of gut microbiota diversity affected the aging process [43,44]. In other words, the required gut microbiota for the recipient may be different depending on the age group of the donor. Non-relative donors may lead to the same efficacy of FMT if the microbiota type is close to the recipient’s microbiota. These findings may provide an initial step in more efficiently stratified FMT depending upon the donor and the recipient.
In long-term evaluation, donor-microbiota stabilization was observed in case #11, wherein, the gut microbiota of recipient was similar to the donor’s microbiota (Figure 6a). The dendrogram showed a high similarity between gut microbiota of the recipient after A-FMT and the donor, thereby indicating that it was stabilized (Figure 6b). However, this finding was not observed clearly in other cases. This fact might suggest the amelioration of clinical indices in other cases without donor-microbiota stabilization, or this is suggestive of the complicated mechanism of the microbial establishment by creating a balance between the recovery of self-microbiota and colonized-microbiota, which struggle with each other [45,46]. Establishment of microbiota can also be affected by specific dietary features and/or antibiotics, as has been reported previously [47,48,49]. It would be difficult to analyze long-term changes in microbiota by minimalizing influences from these factors.
Further, we discuss the beneficial Bacteroidetes species in UC. We have previously reported a decrease in beneficial Bacteroidetes species in UC patients [24]. We found that some specific Bacteroidetes species correlated with the long-term efficacy of FMT, though we analyzed microbiota of a limited number of patients for the long term in A-FMT. These species are known to be predominant in both healthy donors and UC patients [24]. The key bacteria may differ among individuals. Costello et al. showed that anaerobically prepared donor FMT resulted in a higher likelihood of remission [15]. Bacteroidetes are also anaerobic bacteria. The results reported by us are in agreement with other studies [15,50]. Though important bacterial species and metabolites have been identified in various reports [18,51], further evaluation of the intestinal environment is required to understand the interactions among them.
Our study has some limitations. First, this study was non-randomized and conducted at a single center. Second, the clinical response was evaluated only by clinical score. A clinical study, including a randomized controlled trial, is required to evaluate the efficacy of A-FMT regimen.

5. Conclusions

The simple regimen called A-FMT exhibited long-term efficacy as compared to mono-AFM regimen, and it may serve as a useful strategy for managing and maintaining UC. To the best of our knowledge, this is the first report showing the importance of matching between donors and recipients for long-term maintenance by A-FMT in UC. The donor-recipient matching may help to plan the FMT regimen in real clinical practice effectively.
Conference presentation:
  • 15th Congress of ECCO2020 on 12–15 February 2020, in Vienna, Austria. This study won the prize for “Top Ten Best DOPs” during the ECCO2020 conference.
  • 2020 Crohn’s & Colitis Congress on 23–25 January 2020, in Austin, Texas, USA.
  • 61st Annual Meeting of the Japanese Society of Gastroenterology on 21–24 November 2019, in Kobe, Japan.

Supplementary Materials

The following are available online at https://www.mdpi.com/2077-0383/9/6/1650/s1, Figure S1: Comparison of the sum of Mayo endoscopic score between responders and non-responders in the mono-AFM and A-FMT groups during the short-term evaluation, Figure S2: Short-term efficacy of A-FMT compared by ongoing and past medication with anti-tumor necrosis factor α and corticosteroid, Table S1: Microbial analysis data of five patients who were maintained without recurrence for 24 months.

Author Contributions

Conceptualization, D.I. and T.O.; methodology, D.I.; validation, D.I.; formal analysis, D.I. and K.O.; investigation, K.N., S.I., K.H., M.T., and T.S.; data curation, D.I. and K.O.; writing—original draft preparation, K.O.; writing—review and editing, D.I.; visualization, D.I. and K.O.; supervision, A.N.; project administration, D.I.; resources, K.N., S.I., K.H., M.T., and T.S.; software, D.I.; funding acquisition, D.I. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a grant from the Japan Society for the Promotion of Science KAKENHI (grant number JP16K09328) and Kyowa Kirin Co. Ltd.

Acknowledgments

We thank Takashi Sasaki, Yu Jie Lu, Tadashi Baba, Keiichi Hiramatsu (Center of Excellence for Infection Control Science, Graduate School of Medicine, Juntendo University), Kyoko Kuwahara-Arai, Teruo Kirikae (Microbiology, School of Medicine, Juntendo University), and Toshihiro Mita (Parasitology, School of Medicine, Juntendo University) for expert technical assistance. We are also grateful to Maya Kobayashi, Yoko Sugiura, and Tsubasa Nagaoka for general support.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Bajaj, J.S.; Kassam, Z.; Fagan, A.; Gavis, E.A.; Liu, E.; Cox, I.J.; Kheradman, R.; Heuman, U.; Wang, J.; Gurry, T.; et al. Fecal microbiota transplant from a rational stool donor improves hepatic encephalopathy: A randomized clinical trial. Hepatology 2017, 66, 1727–1738. [Google Scholar] [CrossRef] [PubMed]
  2. Halkjær, S.I.; Christensen, A.H.; Lo, B.Z.S.; Browne, P.D.; Günther, S.; Hansen, L.H.; Petersen, A. Faecal microbiota transplantation alters gut microbiota in patients with irritable bowel syndrome: Results from a randomised, double-Blind placebo-controlled study. Gut 2018, 67, 2107–2115. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Li, Q.; Han, Y.; Dy, A.B.; Hagerman, R.J. The Gut Microbiota and Autism Spectrum Disorders. Front. Cell. Neurosci. 2017, 11, 120. [Google Scholar] [CrossRef] [PubMed]
  4. Tang, R.; Wei, Y.; Li, Y.; Chen, W.; Chen, H.; Wang, Q.; Yang, F.; Miao, Q.; Xiao, X.; Zhang, H.; et al. Gut microbial profile is altered in primary biliary cholangitis and partially restored after UDCA therapy. Gut 2017, 67, 534–541. [Google Scholar] [CrossRef] [PubMed]
  5. Tian, H.; Ge, X.; Nie, Y.; Yang, L.; Ding, C.; McFarland, L.V.; Zhang, X.; Chen, Q.; Gong, J.; Li, N. Fecal microbiota transplantation in patients with slow-transit constipation: A randomized, clinical trial. PLoS ONE 2017, 12, e0171308. [Google Scholar] [CrossRef]
  6. Vrieze, A.; Van Nood, E.; Holleman, F.; Salojärvi, J.; Kootte, R.S.; Bartelsman, J.F.; Dallinga–Thie, G.M.; Ackermans, M.T.; Serlie, M.J.; Oozeer, R.; et al. Transfer of Intestinal Microbiota From Lean Donors Increases Insulin Sensitivity in Individuals With Metabolic Syndrome. Gastroenterology 2012, 143, 913–916.e7. [Google Scholar] [CrossRef]
  7. Kang, D.-W.; Adams, J.B.; Coleman, D.M.; Pollard, E.L.; Maldonado, J.; McDonough-Means, S.; Caporaso, J.G.; Krajmalnik-Brown, R. Long-Term benefit of Microbiota Transfer Therapy on autism symptoms and gut microbiota. Sci. Rep. 2019, 9, 5821. [Google Scholar] [CrossRef]
  8. Van Nood, E.; Vrieze, A.; Nieuwdorp, M.; Fuentes, S.; Zoetendal, E.G.; De Vos, W.M.; Visser, C.E.; Kuijper, E.J.; Bartelsman, J.F.; Tijssen, J.G.; et al. Duodenal Infusion of Donor Feces for RecurrentClostridium difficile. N. Engl. J. Med. 2013, 368, 407–415. [Google Scholar] [CrossRef] [Green Version]
  9. Borody, T.J.; Khoruts, A. Fecal microbiota transplantation and emerging applications. Nat. Rev. Gastroenterol. Hepatol. 2011, 9, 88–96. [Google Scholar] [CrossRef]
  10. Hedin, C.; Van Der Gast, C.J.; Rogers, G.B.; Cuthbertson, L.; McCartney, S.; Stagg, A.J.; Lindsay, J.O.; Whelan, K. Siblings of patients with Crohn’s disease exhibit a biologically relevant dysbiosis in mucosal microbial metacommunities. Gut 2015, 65, 944–953. [Google Scholar] [CrossRef] [Green Version]
  11. Braun, J.M.; Wei, B. Body Traffic: Ecology, Genetics, and Immunity in Inflammatory Bowel Disease. Annu. Rev. Pathol. Mech. Dis. 2007, 2, 401–429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Kump, P.; Wurm, P.; Gröchenig, H.P.; Wenzl, H.; Petritsch, W.; Halwachs, B.; Wagner, M.; Stadlbauer, V.; Eherer, A.; Hoffmann, K.M.; et al. The taxonomic composition of the donor intestinal microbiota is a major factor influencing the efficacy of faecal microbiota transplantation in therapy refractory ulcerative colitis. Aliment. Pharmacol. Ther. 2017, 47, 67–77. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Reiff, C.; Kelly, D.; Meharg, C. Inflammatory bowel disease, gut bacteria and probiotic therapy. Int. J. Med. Microbiol. 2010, 300, 25–33. [Google Scholar] [CrossRef] [PubMed]
  14. Sheehan, D.; Shanahan, F. The Gut Microbiota in Inflammatory Bowel Disease. Gastroenterol. Clin. N. Am. 2017, 46, 143–154. [Google Scholar] [CrossRef] [PubMed]
  15. Costello, S.P.; Hughes, P.A.; Waters, O.; Bryant, R.V.; Vincent, A.D.; Blatchford, P.; Katsikeros, R.; Makanyanga, J.; Campaniello, M.A.; Mavrangelos, C.; et al. Effect of Fecal Microbiota Transplantation on 8-Week Remission in Patients With Ulcerative Colitis. JAMA 2019, 321, 156–164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Moayyedi, P.; Surette, M.; Kim, P.T.; Libertucci, J.; Wolfe, M.; Onischi, C.; Armstrong, D.; Marshall, J.K.; Kassam, Z.; Reinisch, W.; et al. Fecal Microbiota Transplantation Induces Remission in Patients with Active Ulcerative Colitis in a Randomized Controlled Trial. Gastroenterology 2015, 149, 102–109.e6. [Google Scholar] [CrossRef] [Green Version]
  17. Paramsothy, S.; Kamm, M.A.; Kaakoush, N.O.; Walsh, A.J.; Bogaerde, J.V.D.; Samuel, D.; Leong, R.W.; Connor, S.; Ng, W.; Paramsothy, R.; et al. Multidonor intensive faecal microbiota transplantation for active ulcerative colitis: A randomised placebo-controlled trial. Lancet 2017, 389, 1218–1228. [Google Scholar] [CrossRef]
  18. Rossen, N.G.; Fuentes, S.; Van Der Spek, M.J.; Tijssen, J.G.; Hartman, J.H.; Duflou, A.; Löwenberg, M.; Brink, G.R.; Mathus-Vliegen, E.M.; de Vos, W.M.; et al. Findings From a Randomized Controlled Trial of Fecal Transplantation for Patients With Ulcerative Colitis. Gastroenterology 2015, 149, 110–118.e4. [Google Scholar] [CrossRef]
  19. Tian, Y.; Zhou, Y.; Huang, S.; Li, J.; Zhao, K.; Li, X.; Wen, X.; Li, X.-A. Fecal microbiota transplantation for ulcerative colitis: A prospective clinical study. BMC Gastroenterol. 2019, 19, 116. [Google Scholar] [CrossRef] [Green Version]
  20. Youngster, I.; Sauk, J.; Pindar, C.; Wilson, R.G.; Kaplan, J.L.; Smith, M.B.; Alm, E.J.; Gevers, D.; Russell, G.H.; Hohmann, E.L. Fecal Microbiota Transplant for Relapsing Clostridium difficile Infection Using a Frozen Inoculum From Unrelated Donors: A Randomized, Open-Label, Controlled Pilot Study. Clin. Infect. Dis. 2014, 58, 1515–1522. [Google Scholar] [CrossRef]
  21. Ding, X.; Li, Q.; Li, P.; Zhang, T.; Cui, B.; Ji, G.; Lu, X.; Zhang, F. Long-Term Safety and Efficacy of Fecal Microbiota Transplant in Active Ulcerative Colitis. Drug Saf. 2019, 42, 869–880. [Google Scholar] [CrossRef] [PubMed]
  22. Lozupone, C.A.; Stombaugh, J.I.; Gordon, J.I.; Jansson, J.K.; Knight, R. Diversity, stability and resilience of the human gut microbiota. Nature 2012, 489, 220–230. [Google Scholar] [CrossRef] [Green Version]
  23. Ishikawa, D.; Haga, K.; Shibuya, T.; Sasaki, T.; Osada, T.; Kuwahara-Arai, K.; Hiramatsu, K.; Watanabe, S. Changes in Intestinal Microbiota Following Combination Therapy with Fecal Microbial Transplantation and Antibiotics for Ulcerative Colitis. Inflamm. Bowel Dis. 2017, 23, 116–125. [Google Scholar] [CrossRef] [PubMed]
  24. Ishikawa, D.; Sasaki, T.; Takahashi, M.; Kuwahara-Arai, K.; Haga, K.; Ito, S.; Okahara, K.; Nakajima, A.; Shibuya, T.; Osada, T.; et al. The Microbial Composition of Bacteroidetes Species in Ulcerative Colitis Is Effectively Improved by Combination Therapy With Fecal Microbiota Transplantation and Antibiotics. Inflamm. Bowel Dis. 2018, 24, 2590–2598. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Yoshino, T.; Nakase, H.; Ueno, S.; Uza, N.; Inoue, S.; Mikami, S.; Matsuura, M.; Ohmori, K.; Sakurai, T.; Nagayama, S.; et al. Usefulness of quantitative real-time PCR assay for early detection of cytomegalovirus infection in patients with ulcerative colitis refractory to immunosuppressive therapies. Inflamm. Bowel Dis. 2007, 13, 1516–1521. [Google Scholar] [CrossRef]
  26. Owens, C.; Broussard, E.; Surawicz, C. Fecal microbiota transplantation and donor standardization. Trends Microbiol. 2013, 21, 443–445. [Google Scholar] [CrossRef]
  27. Rossen, N.G.; Macdonald, J.K.; De Vries, E.M.; D’Haens, G.R.; De Vos, W.M.; Zoetendal, E.G.; Ponsioen, C.Y. Fecal microbiota transplantation as novel therapy in gastroenterology: A systematic review. World J. Gastroenterol. 2015, 21, 5359–5371. [Google Scholar] [CrossRef]
  28. Turner, S.; Pryer, K.M.; Miao, V.P.W.; Palmer, J.D. Investigating deep phylogenetic relationships among cyanobacteria and plastids by small subunit rRNA sequence analysis. J. Eukaryot. Microbiol. 1999, 46, 327–338. [Google Scholar] [CrossRef]
  29. Osada, T.; Ohkusa, T.; Okayasu, I.; Yoshida, T.; Hirai, S.; Beppu, K.; Shibuya, T.; Sakamoto, N.; Kobayashi, O.; Nagahara, A.; et al. Correlations among total colonoscopic findings, clinical symptoms, and laboratory markers in ulcerative colitis. J. Gastroenterol. Hepatol. 2008, 23, S262–S267. [Google Scholar] [CrossRef]
  30. Morisita, M. Measuring of interspecific association and similarity between communities. Mem. Fac. Sci. Kyushu Univ. Ser. E 1959, 3, 65–80. [Google Scholar]
  31. Kimoto, S. Some quantitative analysis on the Chrysomelid fauna of the Ryukyu Archipelago. Esakia 1967, 6, 27–54. [Google Scholar]
  32. Horn, H.S. Measurement of "Overlap" in Comparative Ecological Studies. Am. Nat. 1966, 100, 419–424. [Google Scholar] [CrossRef]
  33. Burrello, C.; Giuffrè, M.R.; Macandog, A.D.; Diaz-Basabe, A.; Cribiù, F.M.; Lopez, G.; Borgo, F.C.; Nezi, L.; Caprioli, F.; Vecchi, M.; et al. Fecal Microbiota Transplantation Controls Murine Chronic Intestinal Inflammation by Modulating Immune Cell Functions and Gut Microbiota Composition. Cells 2019, 8, 517. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Okai, S.; Usui, F.; Ohta, M.; Mori, H.; Kurokawa, K.; Matsumoto, S.; Kato, T.; Miyauchi, E.; Ohno, H.; Shinkura, R. Intestinal IgA as a modulator of the gut microbiota. Gut Microbes 2017, 8, 486–492. [Google Scholar] [CrossRef] [Green Version]
  35. Kassam, Z.; Lee, C.H.; Yuan, Y.; Hunt, R.H. Fecal microbiota transplantation for Clostridium difficile infection: Systematic review and meta-analysis. Am. J. Gastroenterol. 2013, 108, 500–508. [Google Scholar] [CrossRef]
  36. Osman, M.; Stoltzner, Z.; O’Brien, K.; Ling, K.; Koelsch, E.; Dubois, N.; Amaratunga, K.; Smith, M.; Kassam, Z. Donor Efficacy in Fecal Microbiota Transplantation for Recurrent Clostridium difficile: Evidence from a 1,999-Patient Cohort. Open Forum Infect. Dis. 2016, 3, 841. [Google Scholar] [CrossRef]
  37. Vermeire, S.; Joossens, M.; Verbeke, K.; Wang, J.; Machiels, K.; Sabino, J.; Ferrante, M.; Van Assche, G.; Rutgeerts, P.; Raes, J. Donor Species Richness Determines Faecal Microbiota Transplantation Success in Inflammatory Bowel Disease. J. Crohn’s Colitis 2015, 10, 387–394. [Google Scholar] [CrossRef] [Green Version]
  38. Suez, J.; Zmora, N.; Zilberman-Schapira, G.; Mor, U.; Dori-Bachash, M.; Bashiardes, S.; Zur, M.; Regev-Lehavi, D.; Brik, R.B.-Z.; Federici, S.; et al. Post-Antibiotic Gut Mucosal Microbiome Reconstitution Is Impaired by Probiotics and Improved by Autologous FMT. Cell 2018, 174, 1406–1423.e16. [Google Scholar] [CrossRef] [Green Version]
  39. Hedin, C.; Van Der Gast, C.J.; Stagg, A.J.; Lindsay, J.O.; Whelan, K. The gut microbiota of siblings offers insights into microbial pathogenesis of inflammatory bowel disease. Gut Microbes 2017, 8, 359–365. [Google Scholar] [CrossRef] [Green Version]
  40. Palmer, C.; Bik, E.M.; DiGiulio, D.B.; Relman, D.A.; Brown, P.O. Development of the human infant intestinal microbiota. PLoS Biol. 2007, 5, e177. [Google Scholar] [CrossRef] [Green Version]
  41. Stewart, C.J.; Ajami, N.J.; O’Brien, J.L.; Hutchinson, D.S.; Smith, D.; Wong, M.C.; Ross, M.C.; Lloyd, R.E.; Doddapaneni, H.; Metcalf, G.; et al. Temporal development of the gut microbiome in early childhood from the TEDDY study. Nature 2018, 562, 583–588. [Google Scholar] [CrossRef] [PubMed]
  42. Wilson, B.C.; Vatanen, T.; Cutfield, W.S.; O’Sullivan, J.M. The Super-Donor Phenomenon in Fecal Microbiota Transplantation. Front. Microbiol. 2019, 9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Garcia-Pena, C.; Alvarez-Cisneros, T.; Quiroz-Baez, R.; Friedland, R.P. Microbiota and aging. A review and commentary. Arch. Med. Res. 2017, 48, 681–689. [Google Scholar] [CrossRef] [PubMed]
  44. Girotra, M.; Garg, S.; Anand, R.; Song, Y.; Dutta, S.K. Fecal Microbiota Transplantation for Recurrent Clostridium difficile Infection in the Elderly: Long-Term Outcomes and Microbiota Changes. Dig. Dis. Sci. 2016, 61, 3007–3015. [Google Scholar] [CrossRef]
  45. Milani, C.; Duranti, S.; Bottacini, F.; Casey, E.; Turroni, F.; Mahony, J.; Belzer, C.; Palacio, S.D.; Montes, S.A.; Mancabelli, L.; et al. The First Microbial Colonizers of the Human Gut: Composition, Activities, and Health Implications of the Infant Gut Microbiota. Microbiol. Mol. Biol. Rev. 2017, 81, e00036-17. [Google Scholar] [CrossRef] [Green Version]
  46. Palleja, A.; Mikkelsen, K.H.; Forslund, S.K.; Kashani, A.; Allin, K.H.; Nielsen, T.S.; Hansen, T.H.; Liang, S.; Feng, Q.; Zhang, C.; et al. Recovery of gut microbiota of healthy adults following antibiotic exposure. Nat. Microbiol. 2018, 3, 1255–1265. [Google Scholar] [CrossRef]
  47. Schirmer, M.; Franzosa, E.A.; Lloyd-Price, J.; McIver, L.J.; Schwager, R.; Poon, T.W.; Ananthakrishnan, A.N.; Andrews, E.; Barron, G.; Lake, K.; et al. Dynamics of metatranscription in the inflammatory bowel disease gut microbiome. Nat. Microbiol. 2018, 3, 337–346. [Google Scholar] [CrossRef]
  48. Wu, G.D.; Chen, J.; Hoffmann, C.; Bittinger, K.; Chen, Y.-Y.; Keilbaugh, S.A.; Bewtra, M.; Knights, D.; Walters, W.A.; Knight, R.; et al. Linking Long-Term Dietary Patterns with Gut Microbial Enterotypes. Science 2011, 334, 105–108. [Google Scholar] [CrossRef] [Green Version]
  49. Zimmer, J.; Lange, B.; Frick, J.-S.; Sauer, H.; Zimmermann, K.; Schwiertz, A.; Rusch, K.; Klosterhalfen, S.; Enck, P. A vegan or vegetarian diet substantially alters the human colonic faecal microbiota. Eur. J. Clin. Nutr. 2011, 66, 53–60. [Google Scholar] [CrossRef]
  50. Papanicolas, L.E.; Choo, J.M.; Wang, Y.; Leong, L.E.; Costello, S.P.; Gordon, D.L.; Wesselingh, S.L.; Rogers, G.B. Bacterial viability in faecal transplants: Which bacteria survive? EBioMedicine 2019, 41, 509–516. [Google Scholar] [CrossRef] [Green Version]
  51. Paramsothy, S.; Nielsen, S.; Kamm, M.A.; Deshpande, N.P.; Faith, J.J.; Clemente, J.C.; Paramsothy, R.; Walsh, A.J.; Bogaerde, J.V.D.; Samuel, D.; et al. Specific Bacteria and Metabolites Associated With Response to Fecal Microbiota Transplantation in Patients With Ulcerative Colitis. Gastroenterology 2018, 156, 1440–1454.e2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Flow diagram of this study for short-term evaluation. Ninety-two patients were enrolled in our study: 37 patients in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group and 55 patients in the A-FMT (fresh fecal microbiota transplantation (FMT) following AFM) group were assessed for clinical response and remission using intention-to-treat analysis. In the A-FMT group, 31 patients (56.3%) showed a clinical response and 19 (34.5%) achieved clinical remission. These rates were higher than the rates in the mono-AFM group (clinical response/remission: n = 18/6, 48.6%/16.2%), but the difference was not statistically significant.
Figure 1. Flow diagram of this study for short-term evaluation. Ninety-two patients were enrolled in our study: 37 patients in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group and 55 patients in the A-FMT (fresh fecal microbiota transplantation (FMT) following AFM) group were assessed for clinical response and remission using intention-to-treat analysis. In the A-FMT group, 31 patients (56.3%) showed a clinical response and 19 (34.5%) achieved clinical remission. These rates were higher than the rates in the mono-AFM group (clinical response/remission: n = 18/6, 48.6%/16.2%), but the difference was not statistically significant.
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Figure 2. Comparison of the clinical response rate and remission rate by disease distribution between the mono-AFM and A-FMT groups during short-term evaluation. Although no significant difference was observed in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the response and remission rates were significantly higher in patients with proctitis than in those with left-sided and extensive colitis in the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group (left-sided and extensive colitis, n = 46; proctitis, n = 9; clinical response, p = 0.06; clinical remission, p = 0.005, chi-square test).
Figure 2. Comparison of the clinical response rate and remission rate by disease distribution between the mono-AFM and A-FMT groups during short-term evaluation. Although no significant difference was observed in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the response and remission rates were significantly higher in patients with proctitis than in those with left-sided and extensive colitis in the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group (left-sided and extensive colitis, n = 46; proctitis, n = 9; clinical response, p = 0.06; clinical remission, p = 0.005, chi-square test).
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Figure 3. Flow diagram for long-term evaluation of patients who showed effects at 4 weeks after treatment. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy ( amoxicillin, fosfomycin, and metronidazole)) group, 13 patients did not experience relapse within 12 months, and 10 patients did not experience relapse within 24 months after receiving A-FMT. In the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, 6 patients did not experience relapse within 12 months, and 4 patients did not experience relapse within 24 months after AFM administration. * One patient in the A-FMT group was excluded because of the detection of dysplasia.
Figure 3. Flow diagram for long-term evaluation of patients who showed effects at 4 weeks after treatment. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy ( amoxicillin, fosfomycin, and metronidazole)) group, 13 patients did not experience relapse within 12 months, and 10 patients did not experience relapse within 24 months after receiving A-FMT. In the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, 6 patients did not experience relapse within 12 months, and 4 patients did not experience relapse within 24 months after AFM administration. * One patient in the A-FMT group was excluded because of the detection of dysplasia.
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Figure 4. Comparison of cumulative non-relapse rate between the mono-AFM and A-FMT groups. The cumulative non-relapse rate for 24 months was significantly higher in the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group than in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group (p = 0.034, Gehan-Breslow-Wilcoxon test).
Figure 4. Comparison of cumulative non-relapse rate between the mono-AFM and A-FMT groups. The cumulative non-relapse rate for 24 months was significantly higher in the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group than in the mono-AFM (triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group (p = 0.034, Gehan-Breslow-Wilcoxon test).
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Figure 5. (a) Comparison of the cumulative non-relapse rate by the age difference between donors and patients in the A-FMT group. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the ≥11-year difference group (n = 14) showed significantly lower cumulative non-relapse rate than the 0–10-year difference group (n = 16) for 24 months (p = 0.003, log-rank test). (b) Comparison of cumulative non-relapse rate by the relationship between donors and patients in the A-FMT group. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, sibling FMT (n = 7) had a significantly higher cumulative remission rate than parent-child FMT (n = 13) for 24 months (p = 0.007, log-rank test).
Figure 5. (a) Comparison of the cumulative non-relapse rate by the age difference between donors and patients in the A-FMT group. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the ≥11-year difference group (n = 14) showed significantly lower cumulative non-relapse rate than the 0–10-year difference group (n = 16) for 24 months (p = 0.003, log-rank test). (b) Comparison of cumulative non-relapse rate by the relationship between donors and patients in the A-FMT group. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, sibling FMT (n = 7) had a significantly higher cumulative remission rate than parent-child FMT (n = 13) for 24 months (p = 0.007, log-rank test).
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Figure 6. (a) Change in microbiota composition of a patient before and after A-FMT with respect to Bacteroidetes species as compared to the donor. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the change in the composition of Bacteroidetes species in 10 samples (donor, patient before FMT, at 2 weeks, 1, 2, 3, 5, 6, 12, and 24 months after FMT) in case #11. (b) Example of long-term endoscopic outcome after A-FMT. Case #11: A 30-year-old man with a history of extensive ulcerative colitis for three years. He did not take any medication, such as 5-aminosalicylate treatment, PSL or anti-TNFα. He received A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) from his younger brother.
Figure 6. (a) Change in microbiota composition of a patient before and after A-FMT with respect to Bacteroidetes species as compared to the donor. In the A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) group, the change in the composition of Bacteroidetes species in 10 samples (donor, patient before FMT, at 2 weeks, 1, 2, 3, 5, 6, 12, and 24 months after FMT) in case #11. (b) Example of long-term endoscopic outcome after A-FMT. Case #11: A 30-year-old man with a history of extensive ulcerative colitis for three years. He did not take any medication, such as 5-aminosalicylate treatment, PSL or anti-TNFα. He received A-FMT (fresh fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole)) from his younger brother.
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Table 1. Comparison of the baseline characteristics of patients who received mono-AFM and A-FMT.
Table 1. Comparison of the baseline characteristics of patients who received mono-AFM and A-FMT.
All
(n = 92)
Mono-AFM
(n = 37)
A-FMT
(n = 55)
P Value
Age (years)41.1 ± 13.942.5 ± 14.740.1 ± 13.30.42
Sex (M/F)56/3618/1938/170.049
Duration of disease (years)8.7 ± 8.18.9 ± 9.08.6 ± 7.40.83
Disease location
 Proctitis13490.66
 Left-sided colitis2711160.95
 Extensive colitis5222300.64
Ongoing/past treatment
 5-ASA78/8632/3546/510.94/1
 Corticosteroid30/6714/3016/370.38/0.22
 Apheresis1/380/191/190/0.11
 Azathioprine20/387/1613/220.78/0.76
 Tacrolimus6/162/54/110.47/0.60
 Anti-TNF16/356/1210/230.97/0.36
CAI score10.1 ± 2.79.6 ± 2.310.3 ± 2.90.21
 ≥113611250.13
 6–105325280.11
 ≤53120.06
Endoscopic evaluation
 UCEIS4.4 ± 2.43.8 ± 2.04.7 ± 2.50.12
 Mayo endoscopic score1.9 ± 0.71.8 ± 0.81.9 ± 0.70.86
 Sum of Mayo endoscopic scores6.3 ± 4.26.3 ± 4.36.3 ± 4.10.99
A-FMT: fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole); Mono-AFM: triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole); 5-ASA: 5-aminosalicylic acid; Anti-TNF: anti-tumor necrosis factor; UCEIS: ulcerative colitis endoscopic index of severity.
Table 2. Baseline characteristic of responders treated with A-FMT.
Table 2. Baseline characteristic of responders treated with A-FMT.
CaseAge & SexDuration of UC (years)Type of UCDonorDonor
Age
& Sex
Age
Difference (years)
Decrease in CAI ScoreSum of Mayo Endoscopic ScoresDuration of Maintenance (months)
#127M9ExtensiveMother59F32493
#224M6ExtensiveMother48F245910
#326F0.5Left-sidedFather58M32449
#462M1ProctitisSpouse58F48124 *
#532M10ProctitisSpouse29F3713
#636M3ProctitisSpouse30F69124 *
#743M2.5Left-sidedSpouse43F0927
#822F1.5Left-sidedFather56M347224 *
#946M26ExtensiveSpouse49F313102
#1061F24ProctitisDaughter32F29315
#1130M3.5ExtensiveBrother27M381224 *
#1237M6ExtensiveSpouse35F24818
#1360F5ExtensiveDaughter26F345523
#1455F6ProctitisSister53F23116
#1565M23ExtensiveDaughter32F333124
#1647M27ProctitisSpouse46F13424 *
#1746F5ExtensiveSister49F35224 *
#1831M14ProctitisFather66M33416
#1955F34Left-sidedCousin20F351324
#2030M12ExtensiveMother53F23683
#2129M5ExtensiveMother56F27767
#2240M3Left-sidedMother65F25835
#2324F11Left-sidedMother48F24833
#2436M6ExtensiveSpouse43F73117
#2564F13Left-sidedSister58F611524 *
#2673F14ExtensiveSister65F86724 *
#2732M12ExtensiveSister30F21282
#2826M5Left-sidedSister25F14224 *
#2943F7Left-sidedSpouse46M312524 *
#3033M15ProctitisFather66M33632
* The patients did not have a relapse for 24 months. A-FMT: fecal microbiota transplantation (FMT) following triple antibiotic therapy (amoxicillin, fosfomycin, and metronidazole); CAI: clinical activity index; UC: ulcerative colitis.
Table 3. Types of Bacteroidetes species that existed in donors and continued to exist in five patients who maintained without recurrence for 24 months.
Table 3. Types of Bacteroidetes species that existed in donors and continued to exist in five patients who maintained without recurrence for 24 months.
Bacteroidetes Species
Case #4Bacteroides uniformis**, Parabacteroides distasonis**, Bacteroides dorei*, Prevotella copri
Case #6Bacteroides uniformis**, Parabacteroides distasonis**, Bacteroides dorei*, Alistipes putredinis, Alistipes onderdonkii, Bacteroides plebeius, Bacteroides coprocola, Bacteroides massiliensis, Bacteroides vulgatus, Bacteroides thetaiotaomicron, Bacteroides caccae, Bacteroides stercoris, Bacteroides rodentium, Parabacteroides merdae, Paraprevotella xylaniphila
Case #11Bacteroides uniformis**, Parabacteroides distasonis**, Bacteroides dorei*, Alistipes putredinis, Alistipes onderdonkii, Bacteroides massiliensis, Bacteroides vulgatus, Bacteroides thetaiotaomicron Bacteroides caccae, Bacteroides clarus
Case #25Bacteroides uniformis**, Parabacteroides distasonis**, Bacteroides dorei*,
Bacteroides massiliensis, Bacteroides vulgatus, Bacteroides thetaiotaomicron
Case #29Bacteroides uniformis**, Parabacteroides distasonis**, Alistipes putredinis,
Alistipes onderdonkii*, Parabacteroides merdae
** Species were observed in all five cases. * Species were observed in 4 out of 5 cases.

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Okahara, K.; Ishikawa, D.; Nomura, K.; Ito, S.; Haga, K.; Takahashi, M.; Shibuya, T.; Osada, T.; Nagahara, A. Matching between Donors and Ulcerative Colitis Patients Is Important for Long-Term Maintenance after Fecal Microbiota Transplantation. J. Clin. Med. 2020, 9, 1650. https://doi.org/10.3390/jcm9061650

AMA Style

Okahara K, Ishikawa D, Nomura K, Ito S, Haga K, Takahashi M, Shibuya T, Osada T, Nagahara A. Matching between Donors and Ulcerative Colitis Patients Is Important for Long-Term Maintenance after Fecal Microbiota Transplantation. Journal of Clinical Medicine. 2020; 9(6):1650. https://doi.org/10.3390/jcm9061650

Chicago/Turabian Style

Okahara, Koki, Dai Ishikawa, Kei Nomura, Shoko Ito, Keiichi Haga, Masahito Takahashi, Tomoyoshi Shibuya, Taro Osada, and Akihito Nagahara. 2020. "Matching between Donors and Ulcerative Colitis Patients Is Important for Long-Term Maintenance after Fecal Microbiota Transplantation" Journal of Clinical Medicine 9, no. 6: 1650. https://doi.org/10.3390/jcm9061650

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