Infections in Solid Organ Transplant Recipients

A special issue of Microorganisms (ISSN 2076-2607). This special issue belongs to the section "Medical Microbiology".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 1863

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Guest Editor
Department of Clinical Medicine and Surgery,Section of Infectious Diseases, University of Naples "Federico II", Naples, Italy
Interests: SARS-CoV-2; pneumonia mortality; infection

Special Issue Information

Dear Colleagues,

Infections pose a significant risk to solid organ transplant recipients due to their compromised immune systems resulting from immunosuppressive therapy. Understanding the microbiological aspects of infections in this vulnerable population is crucial for early detection, effective management, and improved patient outcomes.

Solid organ transplant recipients are susceptible to a wide range of infectious agents, including bacteria, viruses, fungi, and parasites. Bacterial infections commonly involve surgical site infections, urinary tract infections, pneumonia, and bloodstream infections. The emergence of drug-resistant bacterial strains further complicates treatment strategies and highlights the importance of appropriate antimicrobial stewardship.

Viruses, such as cytomegalovirus, Epstein-Barr virus, and respiratory viruses, can cause significant morbidity and mortality in transplant recipients. Effective antiviral therapies, prophylaxis, and surveillance measures play a vital role in preventing and managing viral infections. Additionally, emerging viral pathogens, like SARS-CoV-2, have posed new challenges during the COVID-19 pandemic, requiring tailored approaches to protect transplant recipients.

Fungal infections, particularly invasive Candida and Aspergillus infections, present substantial risks to solid organ transplant recipients. Rapid diagnosis, targeted antifungal therapy, and careful monitoring of immunosuppressive regimens are crucial in managing these potentially life-threatening infections.

Parasitic infections, although less common, can occur in transplant recipients, particularly in those with travel histories or exposure to endemic regions. Protozoal and helminthic infections necessitate early identification, prompt treatment, and preventive measures.

Microbiological diagnostic techniques, including molecular assays, serology, and culture-based methods, play a pivotal role in identifying causative agents and guiding appropriate antimicrobial therapy. Surveillance programs and infection prevention protocols implemented in transplant centers are essential for detecting outbreaks and implementing timely interventions.

Efforts to mitigate the risk of infections in solid organ transplant recipients involve a multidisciplinary approach involving microbiologists, infectious disease specialists, transplant surgeons, and immunologists. Ongoing research focusing on the pathogenesis, host-pathogen interactions, and novel diagnostic approaches will continue to refine our understanding of infections in this population and aid in the development of preventive strategies and improved patient care.

Some of the focal points include, but are not limited to, the following:

  • management of MDR infections in solid organ transplant patients
  • epidemiology and microbiology of infections in solid organ transplant patients
  • impact of MDR germ infections in solid organ transplant patients
  • new therapeutic options in solid organ transplant patients

Reviews, original research, and communications will be welcome. 

Dr. Biagio Pinchera
Guest Editor

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Published Papers (3 papers)

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18 pages, 2619 KiB  
Article
Monocentric, Retrospective Study on Infectious Complications within One Year after Solid-Organ Transplantation at a Belgian University Hospital
by Céline Van Den Daele, Delphine Martiny, Isabelle Etienne, Delphine Kemlin, Ana Roussoulières, Youri Sokolow, Desislava Germanova, Thierry Gustot, Leda Nobile and Maya Hites
Microorganisms 2024, 12(4), 755; https://doi.org/10.3390/microorganisms12040755 - 09 Apr 2024
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Abstract
The epidemiology, diagnostic methods and management of infectious complications after solid-organ transplantation (SOT) are evolving. The aim of our study is to describe current infectious complications in the year following SOT and risk factors for their development and outcome. We conducted a retrospective [...] Read more.
The epidemiology, diagnostic methods and management of infectious complications after solid-organ transplantation (SOT) are evolving. The aim of our study is to describe current infectious complications in the year following SOT and risk factors for their development and outcome. We conducted a retrospective study in adult SOT recipients in a Belgian university hospital between 2018 and 2019. We gathered demographic characteristics, comorbidities leading to transplantation, clinical, microbiological, surgery-specific and therapeutic data concerning infectious episodes, and survival status up to one year post-transplantation. Two-hundred-and-thirty-one SOT recipients were included (90 kidneys, 79 livers, 35 lungs, 19 hearts and 8 multiple organs). We observed 381 infections in 143 (62%) patients, due to bacteria (235 (62%)), viruses (67 (18%)), and fungi (32 (8%)). Patients presented a median of two (1–5) infections, and the first infection occurred during the first six months. Nineteen (8%) patients died, eleven (58%) due to infectious causes. Protective factors identified against developing infection were obesity [OR [IC]: 0.41 [0.19–0.89]; p = 0.025] and liver transplantation [OR [IC]: 0.21 [0.07–0.66]; p = 0.007]. Risk factors identified for developing an infection were lung transplantation [OR [IC]: 6.80 [1.17–39.36]; p = 0.032], CMV mismatch [OR [IC]: 3.53 [1.45–8.64]; p = 0.006] and neutropenia [OR [IC]: 2.87 [1.27–6.47]; p = 0.011]. Risk factors identified for death were inadequate cytomegalovirus prophylaxis, infection severity and absence of pneumococcal vaccination. Post-transplant infections were common. Addressing modifiable risk factors is crucial, such as pneumococcal vaccination. Full article
(This article belongs to the Special Issue Infections in Solid Organ Transplant Recipients)
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12 pages, 2117 KiB  
Article
BKPyV DNAemia in Kidney Transplant Recipients Undergoing Regular Screening: A Single-Centre Cohort Study
by Daniel B. Rasmussen, Dina L. Møller, Sebastian R. Hamm, Álvaro H. Borges, Alex C. Y. Nielsen, Nikolai S. Kirkby, Søren S. Sørensen and Susanne D. Nielsen
Microorganisms 2024, 12(1), 65; https://doi.org/10.3390/microorganisms12010065 - 29 Dec 2023
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Abstract
Infection with BK polyomavirus (BKPyV) is a common opportunistic infection after kidney transplantation (KT) and may affect graft function. We aimed to determine the incidence, risk factors, and clinical outcomes of BKPyV DNAemia in a prospective cohort of 601 KT recipients transplanted from [...] Read more.
Infection with BK polyomavirus (BKPyV) is a common opportunistic infection after kidney transplantation (KT) and may affect graft function. We aimed to determine the incidence, risk factors, and clinical outcomes of BKPyV DNAemia in a prospective cohort of 601 KT recipients transplanted from 2012 to 2020. BKPyV PCR on plasma was performed at days 60, 90, 180, 270, and 360 post-KT. Any BKPyV DNAemia was defined as a single BKPyV DNA of ≥1000 copies/mL. Severe BKPyV DNAemia was defined as two consecutive BKPyV DNA of ≥10,000 copies/mL. Cumulative incidences were investigated using the Aalen–Johansen estimator, and the risk factors were investigated in Cox proportional hazard models. The incidence of any BKPyV DNAemia and severe BKPyV DNAemia was 21% (18–25) and 13% (10–16) at one year post-KT, respectively. Recipient age > 50 years (aHR, 1.72; 95% CI 1.00–2.94; p = 0.049), male sex (aHR, 1.96; 95% CI 1.17–3.29; p = 0.011), living donors (aHR, 1.65; 95% CI 1.03–2.74; p = 0.045), and >3 HLA-ABDR mismatches (aHR, 1.72; 95% CI 1.01–2.94; p = 0.046) increased the risk of severe BKPyV DNAemia. Any BKPyV DNAemia was associated with an increased risk of graft function decline (aHR, 2.26; 95% CI 1.00–5.12; p = 0.049), and severe BKPyV DNAemia was associated with an increased risk of graft loss (aHR, 3.18; 95% CI 1.06–9.58; p = 0.039). These findings highlight the importance of BKPyV monitoring post-KT. Full article
(This article belongs to the Special Issue Infections in Solid Organ Transplant Recipients)
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18 pages, 5762 KiB  
Systematic Review
Evidence for Immunity against Tetanus, Diphtheria, and Pertussis through Natural Infection or Vaccination in Adult Solid Organ Transplant Recipients: A Systematic Review
by Emil Lenzing, Zitta Barrella Harboe, Søren Schwartz Sørensen, Allan Rasmussen, Susanne Dam Nielsen and Omid Rezahosseini
Microorganisms 2024, 12(5), 847; https://doi.org/10.3390/microorganisms12050847 - 24 Apr 2024
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Abstract
(1) Background: We aim to systematically review the current evidence on immunity against tetanus, diphtheria, and pertussis in adult solid organ transplantation (SOT) recipients, either through natural infection or vaccination. (2) Methods: This systematic review was conducted per PRISMA guidelines. We assessed the [...] Read more.
(1) Background: We aim to systematically review the current evidence on immunity against tetanus, diphtheria, and pertussis in adult solid organ transplantation (SOT) recipients, either through natural infection or vaccination. (2) Methods: This systematic review was conducted per PRISMA guidelines. We assessed the risk of bias using the Cochrane RoB 2 and ROBINS-I and summarized the findings narratively due to the heterogeneity of the studies. (3) Results: Of the 315 screened articles, 11 were included. Tetanus immunity varied between 55% and 86%, diphtheria immunity from 23% to 75%, and pertussis immunity was between 46% and 82%. Post-vaccination immunity showed variation across the studies, with some indicating reductions and others no change, with antibody responses influenced by transplanted organs, gender, age, and immunosuppressive regimens. The single randomized study exhibited a low risk of bias, while of the ten non-randomized studies, six showed moderate and four serious risks of bias, necessitating cautious interpretation of results. (4) Conclusions: SOT recipients exhibit considerable immunity against tetanus and diphtheria at transplantation, but this immunity decreases over time. Although vaccination can enhance this immunity, the response may be suboptimal, and the increased antibody levels may not persist, underscoring the need for tailored vaccination strategies in this vulnerable population. Full article
(This article belongs to the Special Issue Infections in Solid Organ Transplant Recipients)
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