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.

SARS-CoV-2 Immunization Orchestrates the Amplification of IFNγ-Producing T Cell and NK Cell Persistence / L. La Sala, S. Gandini, A. Bruno, R. Allevi, M. Gallazzi, P. Senesi, M.T. Palano, P. Meregalli, E. Longhi, C. Sommese, L. Luzi, E. Trabucchi. - In: FRONTIERS IN IMMUNOLOGY. - ISSN 1664-3224. - 13:(2022 Feb 14), pp. 798813.1-798813.9. [10.3389/fimmu.2022.798813]

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

L. La Sala
Primo
;
R. Allevi;P. Senesi;M.T. Palano;L. Luzi
Penultimo
;
E. Trabucchi
Ultimo
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.
No
English
CD4; CD8; immune response; NK; SARS-CoV-2; vaccines
Settore MED/13 - Endocrinologia
Settore MEDS-02/A - Patologia generale
Settore MEDS-08/A - Endocrinologia
Articolo
Esperti anonimi
Pubblicazione scientifica
Goal 3: Good health and well-being
   Alchilamminoindoli e cicloesilfenoli come smart drugs: caratterizzazione analitica e determinazione analitica in matrici biologiche e non biologiche.
   MINISTERO DELL'ISTRUZIONE E DEL MERITO
   20098KWPMC_001
14-feb-2022
Frontiers Media
13
798813
1
9
9
Pubblicato
Periodico con rilevanza internazionale
scopus
crossref
datacite
Aderisco
info:eu-repo/semantics/article
SARS-CoV-2 Immunization Orchestrates the Amplification of IFNγ-Producing T Cell and NK Cell Persistence / L. La Sala, S. Gandini, A. Bruno, R. Allevi, M. Gallazzi, P. Senesi, M.T. Palano, P. Meregalli, E. Longhi, C. Sommese, L. Luzi, E. Trabucchi. - In: FRONTIERS IN IMMUNOLOGY. - ISSN 1664-3224. - 13:(2022 Feb 14), pp. 798813.1-798813.9. [10.3389/fimmu.2022.798813]
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L. La Sala, S. Gandini, A. Bruno, R. Allevi, M. Gallazzi, P. Senesi, M.T. Palano, P. Meregalli, E. Longhi, C. Sommese, L. Luzi, E. Trabucchi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/914128
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