Abstract | OBJECTIVE: METHODS: In total, 57 cancer patients who received BNT162b2-RNA or BBIBP-CorV vaccines were enrolled. Cellular and humoral immunity were assessed at three-time points, before the first vaccine dose and 14-21 days after the first and second doses. Chemiluminescent microparticle immunoassay was used to evaluate SARS-CoV-2 anti-spike IgG response, and QuantiFERON® SARS-CoV-2 kit assessed T-cell response. RESULTS: Data showed that cancer patients' CD4+ and CD8+ T cell-median IFN-γ secretion of SARS-CoV-2 antigens increased after the first and second vaccine doses (p = 0.027 and p = 0.042). BNT162b2 vaccinees had significantly higher IFN-γ levels to CD4+ and CD8+ T cell epitopes than BBIBP-CorV vaccinees (p = 0.028). There was a positive correlation between IgG antibody titer and T cell response regardless of vaccine type (p < 0.05). CONCLUSIONS: This study is one of the first to investigate cellular and humoral immune responses to SARS-CoV-2 immunization in cancer patients on active therapy after each vaccine dose. COVID-19 immunizations helped cancer patients develop an effective immune response. Understanding the cellular and humoral immune response to COVID-19 in cancer patients undergoing active treatment is necessary to improve vaccines and avoid future SARS pandemics.
|
Authors | Lina Souan, Hikmat Abdel-Razeq, Muna Al Zughbieh, Sara Al Badr, Maher A Sughayer |
Journal | Viruses
(Viruses)
Vol. 15
Issue 7
(06 26 2023)
ISSN: 1999-4915 [Electronic] Switzerland |
PMID | 37515127
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- BIBP COVID-19 vaccine
- COVID-19 Vaccines
- BNT162 Vaccine
- Antibodies, Viral
- Epitopes, T-Lymphocyte
- Immunoglobulin G
|
Topics |
- Humans
- Immunity, Humoral
- COVID-19 Vaccines
- BNT162 Vaccine
- Kinetics
- COVID-19
(prevention & control)
- SARS-CoV-2
- Vaccination
- Antibodies, Viral
- Epitopes, T-Lymphocyte
- Immunoglobulin G
- Neoplasms
|