SARS-CoV-2: Immune Response Elicited by Infection or Vaccination
A special issue of Antibodies (ISSN 2073-4468). This special issue belongs to the section "Humoral Immunity".
Deadline for manuscript submissions: closed (28 February 2024) | Viewed by 14528
Special Issue Editor
Special Issue Information
Dear Colleagues,
The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has inflicted a massive burden on health and the global economy. The infection begins by binding its spike protein S1 region containing the receptor-binding domain (S-RBD) and the N-terminal domain (NTD) to the angiotensin-converting enzyme-2 (ACE-2). Thus, the SARS-CoV-2 S protein became the target for the development of COVID-19 vaccines, which can generate antibodies with potent neutralizing capability. Immunity against SARS-CoV-2 provides protection against infection or, when infection occurs, defense against severe disease.
As with other pathogens, mutations in the SARS-CoV-2 occur spontaneously during replication, producing novel variants that are selected for relevance based on their cellular infectivity, host-to-host transmissibility, or a failure of existing vaccines. Moreover, the viral signals can evade the immune protection conferred by vaccines and natural infection. As a result, the effectiveness of the immune system response to SARS-CoV-2 depends on the strength and breadth of specific antibody and T-cell responses.
Transmission rates and severity of new infections due to COVID-19 decreased post-vaccination. However, the degree, breadth, and durability of protection provided by vaccines remain unclear.
Dr. Elisa Pesce
Guest Editor
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Keywords
- COVID-19
- SARS-CoV-2
- immune response
- vaccines
- vaccine-induced immunity
- natural immunity
- cellular immunity
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