Frontiers in immunology · 2022
Humoral and cellular immune responses to CoronaVac up to one year after vaccination.
Клиническое исследование III фазыСтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Costa Priscilla Ramos, Correia Carolina Argondizo, Marmorato Mariana Prado, Dias Juliana Zanatta de Carvalho, Thomazella Mateus Vailant, Cabral da Silva Amanda, de Oliveira Ana Carolina Soares, Gusmão Arianne Fagotti, Ferrari Lilian, Freitas Angela Carvalho, Patiño Elizabeth González, Grifoni Alba, Weiskopf Daniela, Sette Alessandro, Scharf Rami, Kallás Esper Georges, Silveira Cássia Gisele Terrassani
Аннотация
Coronavac is a widely used SARS-CoV-2 inactivated vaccine, but its long-term immune response assessment is still lacking. We evaluated SARS-CoV-2-specific immune responses, including T cell activation markers, antigen-specific cytokine production and antibody response following vaccination in 53 adult and elderly individuals participating in a phase 3 clinical trial. Activated follicular helper T (Tfh), non-Tfh and memory CD4+ T cells were detected in almost all subjects early after the first vaccine dose. Activated memory CD4+ T cells were predominantly of central and effector memory T cell phenotypes and were sustained for at least 6 months. We also detected a balanced Th1-, Th2- and Th17/Th22-type cytokine production that was associated with response over time, together with particular cytokine profile linked to poor responses in older vaccinees. SARS-CoV-2-specific IgG levels peaked 14 days after the second dose and were mostly stable over one year. CoronaVac was able to induce a potent and durable antiviral antigen-specific cellular response and the cytokine profiles related to the response over time and impacted by the senescence were defined.