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SARS-CoV-2 Immunization Orchestrates the Amplification of IFNγ-Producing T Cell and NK Cell Persistence

Capitolo di libro
Data di Pubblicazione:
2022
Abstract:
A successful vaccination would represent the most efficient means to control the pandemic of Coronavirus Disease-19 (COVID-19) that led to millions of deaths worldwide. Novel mRNA-based vaccines confer protective immunity against SARS-CoV-2, but whether immunity is immediately effective and how long it will remain in recipients are uncertain. We sought to assess the effectiveness of a two-dose regimen since the boosts are often delayed concerning the recommended intervals. Methods: A longitudinal cohort of healthcare workers (HCW, N = 46; 30.4% men; 69.6% women; mean age 36.05 ± 2.2 years) with no SARS-CoV-2 infection as documented by negative polymerase chain reaction was immunophenotyped in PBMC once a week for 4 weeks from the prime immunization (Pfizer mRNA BNT162b2) and had received 2 doses, to study the kinetic response. Results: We identified three risk groups to develop SARS-CoV-2 infection IgG+-based (late responders, R-; early responders, R+; pauci responders, PR). In all receipts, amplification of B cells and NK cells, including IL4-producing B cells and IL4-producing CD8+ T cells, is early stimulated by the vaccine. After the boost, we observed a growing increase of NK cells but a resistance of T cells, IFNγ-producing CD4+T cells, and IFNγ-producing NK cells. Also, hematologic parameters decline until the boost. The positive association of IFNγ-producing NK with IFNγ-producing CD4+T cells by the multiple mixed-effect model, adjusted for confounders (p = 0.036) as well as the correlation matrix (r = 0.6, p < 0.01), suggests a relationship between these two subsets of lymphocytes. Conclusions: These findings introduce several concerns about policy delay in vaccination: based on immunological protection, B cells and the persistent increase of NK cells during 2 doses of the mRNA-based vaccine could provide further immune protection against the virus, while CD8+ T cells increased slightly only in the R+ and PR groups.
Tipologia CRIS:
Articolo in Volume
Keywords:
CD4; CD8; immune response; NK; SARS-CoV-2; vaccines; Adult; B-Lymphocytes; BNT162 Vaccine; COVID-19; Female; Humans; Interferon-gamma; Interleukin-4; Killer Cells, Natural; Leukocytes, Mononuclear; Lymphocyte Subsets; Male; SARS-CoV-2; T-Lymphocytes; Th1-Th2 Balance; Immunization
Elenco autori:
La Sala, L.; Gandini, S.; Bruno, A.; Allevi, R.; Gallazzi, M.; Senesi, P.; Palano, M. T.; Meregalli, P.; Longhi, E.; Sommese, C.; Luzi, L.; Trabucchi, E.
Autori di Ateneo:
BRUNO ANTONINO
Link alla scheda completa:
https://irinsubria.uninsubria.it/handle/11383/2132607
Titolo del libro:
NA
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