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Immune response against the SARS-CoV-2 spike protein in cancer patients after COVID-19 vaccination during the Omicron wave: a prospective study.
- Source :
-
Journal of infection and public health [J Infect Public Health] 2024 Jul; Vol. 17 (7), pp. 102473. Date of Electronic Publication: 2024 Jun 07. - Publication Year :
- 2024
-
Abstract
- Background: Cancer patients often have weakened immune systems, resulting in a lower response to vaccines, especially those receiving immunosuppressive oncological treatment (OT). We aimed to assess the impact of OT on the humoral and T-cell response to the B.1 lineage and Omicron variant following COVID-19 vaccination in patients with solid and hematological neoplasms.<br />Methods: We conducted a prospective study on cancer patients, stratified into OT and non-OT groups, who received a two-dose series of the COVID-19 mRNA vaccine and a booster six months later. The outcomes measured were the humoral (anti-SARS-CoV-2 S IgG titers and ACE2-S interaction inhibition capacity) and cellular (SARS-CoV-2 S-specific T-cell spots per million PBMCs) responses against the B.1 lineage and Omicron variant. These responses were evaluated four weeks after the second dose (n = 98) and eight weeks after the booster dose (n = 71).<br />Results: The humoral response after the second vaccine dose against the B.1 lineage and Omicron variant was significantly weaker in the OT group compared to the non-OT group (q-value<0.05). A booster dose of the mRNA-1273 vaccine significantly improved the humoral response in the OT group, making it comparable to the non-OT group. The mRNA-1273 vaccine, designed for the original Wuhan strain, elicited a weaker humoral response against the Omicron variant compared to the B.1 lineage, regardless of oncological treatment or vaccine dose. In contrast, T-cell responses against SARS-CoV-2, including the Omicron variant, were already present after the second vaccine dose and were not significantly affected by oncological treatments.<br />Conclusions: Cancer patients, particularly those receiving immunosuppressive oncological treatments, should require booster doses and adapted COVID-19 vaccines for new SARS-CoV-2 variants like Omicron. Future studies should evaluate the durability of the immune response and the efficacy of individualized regimens.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
- Subjects :
- Humans
Prospective Studies
Male
Female
Middle Aged
Aged
T-Lymphocytes immunology
Immunization, Secondary
Vaccination
Adult
Immunity, Humoral
Immunoglobulin G blood
Immunocompromised Host
Immunity, Cellular
COVID-19 immunology
COVID-19 prevention & control
COVID-19 Vaccines immunology
COVID-19 Vaccines administration & dosage
Spike Glycoprotein, Coronavirus immunology
SARS-CoV-2 immunology
Neoplasms immunology
Antibodies, Viral blood
Subjects
Details
- Language :
- English
- ISSN :
- 1876-035X
- Volume :
- 17
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of infection and public health
- Publication Type :
- Academic Journal
- Accession number :
- 38865774
- Full Text :
- https://doi.org/10.1016/j.jiph.2024.102473