Protective immunity after COVID-19 has been questioned: what can we do without SARS-CoV-2-IgG detection?

dc.creatorMelgaço, Juliana Gil
dc.creatorAzamor, Tamiris
dc.creatorAno Bom, Ana Paula Dinis
dc.date.accessioned2020-05-14T17:06:40Z
dc.date.available2020-05-14T17:06:40Z
dc.date.issued2020-04-28
dc.description.abstractSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a severe acute respiratory syndrome that is called COVID-19. Clinical manifestations of COVID-19 include diarrhea, pneumonia, lymphopenia, exhausted lymphocytes, and pro-inflammatory cytokine production. Immunology is part of the process of clinical evolution, but there are some questions around immunity-based protection: (1) why some infected people have only mild symptoms of the disease or are asymptomatic; (2) why delayed and weak antibody responses are associated with severe outcomes; and (3) why positivity in molecular tests does not represent protective antibody IgG. Perhaps T cell responses may be the key to solving those questions. SARS-CoV-2-specific memory T cells persist in peripheral blood and may be capable of providing effective information about protective immunity. The T cells studies can be helpful in elucidating the pathways for development of vaccines, therapies, and diagnostics for COVID-19 and for filling these immunology knowledge gaps.pt_BR
dc.identifier.citationMELGAÇO, J. G.; AZAMOR, T.; ANO BOM, A. P. D. Protective immunity after COVID-19 has been questioned: what can we do without SARS-CoV-2-IgG detection? Cellular Immunology, New York, v. 353, July 2020.pt_BR
dc.identifier.urihttps://repositorio.ufla.br/handle/1/40911
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0008874920302501pt_BR
dc.languageen_USpt_BR
dc.publisherElsevierpt_BR
dc.rightsopenAccesspt_BR
dc.sourceCellular Immunologypt_BR
dc.subjectCOVID-19pt_BR
dc.subjectCoronaviruspt_BR
dc.subjectSARS-CoV-2pt_BR
dc.titleProtective immunity after COVID-19 has been questioned: what can we do without SARS-CoV-2-IgG detection?pt_BR
dc.typeArtigopt_BR

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