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Publicação:
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil

dc.contributor.authorCastelli, Erick C. [UNESP]
dc.contributor.authorde Castro, Mateus V.
dc.contributor.authorNaslavsky, Michel S.
dc.contributor.authorScliar, Marilia O.
dc.contributor.authorSilva, Nayane S. B. [UNESP]
dc.contributor.authorPereira, Raphaela N. [UNESP]
dc.contributor.authorCiriaco, Viviane A. O. [UNESP]
dc.contributor.authorCastro, Camila F. B. [UNESP]
dc.contributor.authorMendes-Junior, Celso T.
dc.contributor.authorSilveira, Etiele de S.
dc.contributor.authorde Oliveira, Iuri M.
dc.contributor.authorAntonio, Eduardo C.
dc.contributor.authorVieira, Gustavo F.
dc.contributor.authorMeyer, Diogo
dc.contributor.authorNunes, Kelly
dc.contributor.authorMatos, Larissa R. B.
dc.contributor.authorSilva, Monize V. R.
dc.contributor.authorWang, Jaqueline Y. T.
dc.contributor.authorEsposito, Joyce
dc.contributor.authorCória, Vivian R.
dc.contributor.authorMagawa, Jhosiene Y.
dc.contributor.authorSantos, Keity S.
dc.contributor.authorCunha-Neto, Edecio
dc.contributor.authorKalil, Jorge
dc.contributor.authorBortolin, Raul H.
dc.contributor.authorHirata, Mário Hiroyuki
dc.contributor.authorDell’Aquila, Luiz P.
dc.contributor.authorRazuk-Filho, Alvaro
dc.contributor.authorBatista-Júnior, Pedro B.
dc.contributor.authorDuarte-Neto, Amaro N.
dc.contributor.authorDolhnikoff, Marisa
dc.contributor.authorSaldiva, Paulo H. N.
dc.contributor.authorPassos-Bueno, Maria Rita
dc.contributor.authorZatz, Mayana
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionCentro Universitário Sudoeste Paulista
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)
dc.contributor.institutionUniversidade La Salle
dc.contributor.institutionInstituto Nacional de Ciências e Tecnologia-iii (INCT)
dc.contributor.institutionPrevent Senior Institute
dc.date.accessioned2023-07-29T13:59:32Z
dc.date.available2023-07-29T13:59:32Z
dc.date.issued2022-10-25
dc.description.abstractBackground: Although aging correlates with a worse prognosis for Covid-19, super elderly still unvaccinated individuals presenting mild or no symptoms have been reported worldwide. Most of the reported genetic variants responsible for increased disease susceptibility are associated with immune response, involving type I IFN immunity and modulation; HLA cluster genes; inflammasome activation; genes of interleukins; and chemokines receptors. On the other hand, little is known about the resistance mechanisms against SARS-CoV-2 infection. Here, we addressed polymorphisms in the MHC region associated with Covid-19 outcome in super elderly resilient patients as compared to younger patients with a severe outcome. Methods: SARS-CoV-2 infection was confirmed by RT-PCR test. Aiming to identify candidate genes associated with host resistance, we investigated 87 individuals older than 90 years who recovered from Covid-19 with mild symptoms or who remained asymptomatic following positive test for SARS-CoV-2 as compared to 55 individuals younger than 60 years who had a severe disease or died due to Covid-19, as well as to the general elderly population from the same city. Whole-exome sequencing and an in-depth analysis of the MHC region was performed. All samples were collected in early 2020 and before the local vaccination programs started. Results: We found that the resilient super elderly group displayed a higher frequency of some missense variants in the MUC22 gene (a member of the mucins’ family) as one of the strongest signals in the MHC region as compared to the severe Covid-19 group and the general elderly control population. For example, the missense variant rs62399430 at MUC22 is two times more frequent among the resilient super elderly (p = 0.00002, OR = 2.24). Conclusion: Since the pro-inflammatory basal state in the elderly may enhance the susceptibility to severe Covid-19, we hypothesized that MUC22 might play an important protective role against severe Covid-19, by reducing overactive immune responses in the senior population.en
dc.description.affiliationDepartment of Pathology School of Medicine São Paulo State University (UNESP)
dc.description.affiliationMolecular Genetics and Bioinformatics Laboratory Experimental Research Unit (Unipex) School of Medicine São Paulo State University (UNESP)
dc.description.affiliationHuman Genome and Stem Cell Research Center University of São Paulo
dc.description.affiliationDepartment of Genetics and Evolutionary Biology Biosciences Institute University of São Paulo
dc.description.affiliationCentro Universitário Sudoeste Paulista
dc.description.affiliationDepartamento de Química Faculdade de Filosofa Ciências e Letras de Ribeirão Preto Universidade de São Paulo
dc.description.affiliationPrograma de Pós-Graduação em Genética e Biologia Molecular Universidade Federal do Rio Grande do Sul (UFRGS)
dc.description.affiliationLaboratório de Saúde Humana In Silico Programa de Pós-Graduação em Saúde e Desenvolvimento Humano Universidade La Salle
dc.description.affiliationDepartamento de Clínica Médica Disciplina de Alergia e Imunologia Clínica Faculdade de Medicina da Universidade de São Paulo
dc.description.affiliationLaboratório de Imunologia Instituto do Coração (InCor) Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)
dc.description.affiliationInstituto de Investigação em Imunologia Instituto Nacional de Ciências e Tecnologia-iii (INCT)
dc.description.affiliationDepartment of Clinical and Toxicological Analyses School of Pharmaceutical Sciences University of São Paulo
dc.description.affiliationPrevent Senior Institute
dc.description.affiliationDepartment of Pathology School of Medicine University of Sao Paulo
dc.description.affiliationUnespDepartment of Pathology School of Medicine São Paulo State University (UNESP)
dc.description.affiliationUnespMolecular Genetics and Bioinformatics Laboratory Experimental Research Unit (Unipex) School of Medicine São Paulo State University (UNESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2013/08028-1
dc.description.sponsorshipIdFAPESP: 2013/17084-0
dc.description.sponsorshipIdFAPESP: 2014/50931-3
dc.description.sponsorshipIdFAPESP: 2017/19223-0
dc.description.sponsorshipIdFAPESP: 2019/19998-8
dc.description.sponsorshipIdFAPESP: 2020/09702-1
dc.description.sponsorshipIdCNPq: 465355/2014-5
dc.identifierhttp://dx.doi.org/10.3389/fimmu.2022.975918
dc.identifier.citationFrontiers in Immunology, v. 13.
dc.identifier.doi10.3389/fimmu.2022.975918
dc.identifier.issn1664-3224
dc.identifier.scopus2-s2.0-85141376893
dc.identifier.urihttp://hdl.handle.net/11449/248998
dc.language.isoeng
dc.relation.ispartofFrontiers in Immunology
dc.sourceScopus
dc.subjectCOVID-19
dc.subjectHLA
dc.subjecthuman leukocyte antigens
dc.subjectimmune response
dc.subjectmajor histocompatibility complex (MCH)
dc.subjectMUC22
dc.subjectresistant genetic variants
dc.subjectSARS-CoV-2
dc.titleMUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazilen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt
unesp.departmentMicrobiologia e Imunologia - IBBpt

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