SARS-CoV-2 Variants, Vaccines, and Immunology

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "COVID-19 Vaccines and Vaccination".

Deadline for manuscript submissions: closed (16 July 2023) | Viewed by 4558

Special Issue Editor


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Guest Editor
1. Division of Allergy and Clinical Immunology, Department of Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA
2. Ragon Institute of MGH, MIT and Harvard, Cambridge, MA 02139, USA
Interests: immunology; antibody; B-cells; SARS-CoV-2

Special Issue Information

Dear Colleagues,

SARS-CoV-2 has imposed a global threat and severely impacted the world, with the ongoing COVID-19 pandemic having resulted in millions of hospitalizations and deaths, which has been further exacerbated by the emergence of new variants.

Recent scientific and technological advancements have led to development of multiple vaccines at an unprecedent speed, some of which reached the public within just one year, which is highly encouraging; however, emerging variants have compromised the efficacy of available vaccines and created a pressing need to develop new vaccines. Current research has therefore focused on the development of both new variant-specific and pan-coronaviral vaccines. In addition to vaccines, the efficacy of therapeutic antibodies has also been compromised in the face of evolving variants, which warrants the development of variant-resistant broadly neutralizing antibodies and other therapeutic agents.

Immunity acquired by vaccination or infection naturally fades with time, which further increases the risk of infection or re-infection. However, the rate of fading varies among individuals, where some individuals have a relatively slower rate than others, but the factors influencing this variation are not yet clear. Despite much research having been conducted in a relatively short span of time, a clear understanding of the detailed immune response is still needed. Why are some individuals more susceptible to infection or severe illness; what defines protective immunity and how long it lasts; are there any differences in immunity acquired by different vaccine regimes or with infections, and what factors affect this; and how can the efficacy of vaccines and therapeutic agents be further improved?

For this Special Issue, we invite contributions that focus on the advancement of our understanding of evolving SARS-CoV-2, its immunological responses, and new vaccine strategies. 

We look forward to receiving your valuable contributions.

Dr. Avneesh Gautam
Guest Editor

Manuscript Submission Information

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Keywords

  • COVID-19
  • SARS-CoV-2 and its variants
  • immunological responses
  • vaccine efficacies
  • pan-coronaviral vaccines
  • neutralizing antibodies
  • antibody kinetics and durability

Published Papers (2 papers)

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Research

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13 pages, 677 KiB  
Article
Safety after BBIBP-CorV (Sinopharm) COVID-19 Vaccine in Adolescents Aged 10–17 Years in Thailand
by Saraiorn Thonginnetra, Kriangkrai Tawinprai, Krongkwan Niemsorn, Pathariya Promsena, Manunya Tandhansakul, Naruporn Kasemlawan, Natthanan Ruangkijpaisal, Narin Banomyong, Nanthida Phattraprayoon, Pisuttikan Rangkakulnuwat, Preeda Vanichsetakul, Teerapat Ungtrakul, Kasiruck Wittayasak, Nawarat Thonwirak, Kamonwan Soonklang and Nithi Mahanonda
Vaccines 2022, 10(10), 1765; https://doi.org/10.3390/vaccines10101765 - 21 Oct 2022
Cited by 10 | Viewed by 2201
Abstract
Coronavirus disease 2019 affected child health and impacted learning because of the resulting onsite school closures. This prospective cohort study included children aged 10–17 who received two 4 µg doses of BBIBP-CorV administered intramuscularly 21–28 days apart. To assess vaccine safety, 36,808 participants [...] Read more.
Coronavirus disease 2019 affected child health and impacted learning because of the resulting onsite school closures. This prospective cohort study included children aged 10–17 who received two 4 µg doses of BBIBP-CorV administered intramuscularly 21–28 days apart. To assess vaccine safety, 36,808 participants were then followed with paper- and web-based online questionnaire surveys that captured local and systemic reactogenicities following vaccine administration on days 1, 7, and 30. Among participants, 76% (27,880) reported reactogenicity within the first 24 h and 7 days following the first dose. Half (51.41%) of participants experienced pain at the injection site; the majority of cases were mild in severity. Injection site tenderness (37.93%) was another common local reaction. Fatigue (37.89%), myalgia (33.56%), and headache (26.76%) were the most common systemic reactions. On days 2–7 after the first dose, 25.85% of participants experienced adverse reactions. Following the second dose, reactogenicity was 7.6% and 1.09% within 24 h and between days 2–7. The majority of reactions were of mild to moderate severity. We report that two doses of the BBIBP-CorV caused mild to moderate side effects in adolescents in Thailand. The findings confirm the vaccine’s safety profile in this age group. Full article
(This article belongs to the Special Issue SARS-CoV-2 Variants, Vaccines, and Immunology)
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Review

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7 pages, 1516 KiB  
Review
A Closer Look at ACE2 Signaling Pathway and Processing during COVID-19 Infection: Identifying Possible Targets
by Pia V. Sodhi, Francoise Sidime, David D. Tarazona, Faviola Valdivia and Kelly S. Levano
Vaccines 2023, 11(1), 13; https://doi.org/10.3390/vaccines11010013 - 21 Dec 2022
Cited by 1 | Viewed by 1951
Abstract
Since the identification of its role as the functional receptor for SARS-CoV in 2003 and for SARS-CoV-2 in 2020, ACE2 has been studied in depth to understand COVID-19 susceptibility and severity. ACE2 is a widely expressed protein, and it plays a major regulatory [...] Read more.
Since the identification of its role as the functional receptor for SARS-CoV in 2003 and for SARS-CoV-2 in 2020, ACE2 has been studied in depth to understand COVID-19 susceptibility and severity. ACE2 is a widely expressed protein, and it plays a major regulatory role in the renin–angiotensin–aldosterone System (RAAS). The key to understanding susceptibility and severity may be found in ACE2 variants. Some variants have been shown to affect binding affinity with SARS-CoV-2. In this review, we discuss the role of ACE2 in COVID-19 infection, highlighting the importance of ACE2 isoforms (soluble and membrane-bound) and explore how ACE2 variants may influence an individual’s susceptibility to SARS-CoV-2 infection and disease outcome. Full article
(This article belongs to the Special Issue SARS-CoV-2 Variants, Vaccines, and Immunology)
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