| Autor: |
Nguyen, Huy C, Lal, Kerri G, Balinsky, Corey A, Hontz, Robert D, Lin, Jin, Beye, Matthew J, Smith, Lauren, Pan, Li, Cheng, Ying, Fox, Isabella, Lizewski, Stephen E, Foo, Hayley S, Krebs, Shelly J, Sun, Peifang, Letizia, Andrew G |
| Předmět: |
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| Zdroj: |
Journal of Infectious Diseases; 9/15/2024, Vol. 230 Issue 3, p645-656, 12p |
| Abstrakt: |
Background COVID-19 remains a global public health challenge due to new immune-evasive SARS-CoV-2 variants and heterogeneous immunity. Methods In this cross-sectional study, we evaluated the adaptive immune responses in US active duty personnel who completed a COVID-19 primary vaccine series and had heterogenous SARS-CoV-2 vaccination and infection histories to 3 previously dominant variants (ancestral, Delta, BA.5) and 3 circulating variants (XBB.1.5, EG.5, and BA.2.86) in late 2023. Analyses were based on the most recent exposure in terms of timing (within or beyond 12 months) and type (vaccine or infection). Results Significant reduction was observed in binding antibodies, neutralization antibodies, memory B cells, and CD8+ T cells against circulating variants when compared with previous variants. The reduction in antibody response was more pronounced in those whose most recent exposure was >12 months from enrollment. In contrast, the CD4+ T-cell response was largely consistent across all tested variants. The type of most recent exposure was not a significant factor in determining the magnitude of current immune responses. Conclusions Administration of the XBB.1.5-based booster is likely to enhance cross-reactive humoral responses against SARS-CoV-2 circulating lineages. Ongoing surveillance of immune responses to emerging variants is needed for informing vaccine composition and timing. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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