MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3389/fimmu.2022.975918 http://hdl.handle.net/11449/248998 |
Resumo: | Background: 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. |
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MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from BrazilCOVID-19HLAhuman leukocyte antigensimmune responsemajor histocompatibility complex (MCH)MUC22resistant genetic variantsSARS-CoV-2Background: 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.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Pathology School of Medicine São Paulo State University (UNESP)Molecular Genetics and Bioinformatics Laboratory Experimental Research Unit (Unipex) School of Medicine São Paulo State University (UNESP)Human Genome and Stem Cell Research Center University of São PauloDepartment of Genetics and Evolutionary Biology Biosciences Institute University of São PauloCentro Universitário Sudoeste PaulistaDepartamento de Química Faculdade de Filosofa Ciências e Letras de Ribeirão Preto Universidade de São PauloPrograma de Pós-Graduação em Genética e Biologia Molecular Universidade Federal do Rio Grande do Sul (UFRGS)Laboratório de Saúde Humana In Silico Programa de Pós-Graduação em Saúde e Desenvolvimento Humano Universidade La SalleDepartamento de Clínica Médica Disciplina de Alergia e Imunologia Clínica Faculdade de Medicina da Universidade de São PauloLaboratório de Imunologia Instituto do Coração (InCor) Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)Instituto de Investigação em Imunologia Instituto Nacional de Ciências e Tecnologia-iii (INCT)Department of Clinical and Toxicological Analyses School of Pharmaceutical Sciences University of São PauloPrevent Senior InstituteDepartment of Pathology School of Medicine University of Sao PauloDepartment of Pathology School of Medicine São Paulo State University (UNESP)Molecular Genetics and Bioinformatics Laboratory Experimental Research Unit (Unipex) School of Medicine São Paulo State University (UNESP)FAPESP: 2013/08028-1FAPESP: 2013/17084-0FAPESP: 2014/50931-3FAPESP: 2017/19223-0FAPESP: 2019/19998-8FAPESP: 2020/09702-1CNPq: 465355/2014-5Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Centro Universitário Sudoeste PaulistaUniversidade Federal do Rio Grande do Sul (UFRGS)Universidade La SalleInstituto Nacional de Ciências e Tecnologia-iii (INCT)Prevent Senior InstituteCastelli, Erick C. [UNESP]de Castro, Mateus V.Naslavsky, Michel S.Scliar, Marilia O.Silva, Nayane S. B. [UNESP]Pereira, Raphaela N. [UNESP]Ciriaco, Viviane A. O. [UNESP]Castro, Camila F. B. [UNESP]Mendes-Junior, Celso T.Silveira, Etiele de S.de Oliveira, Iuri M.Antonio, Eduardo C.Vieira, Gustavo F.Meyer, DiogoNunes, KellyMatos, Larissa R. B.Silva, Monize V. R.Wang, Jaqueline Y. T.Esposito, JoyceCória, Vivian R.Magawa, Jhosiene Y.Santos, Keity S.Cunha-Neto, EdecioKalil, JorgeBortolin, Raul H.Hirata, Mário HiroyukiDell’Aquila, Luiz P.Razuk-Filho, AlvaroBatista-Júnior, Pedro B.Duarte-Neto, Amaro N.Dolhnikoff, MarisaSaldiva, Paulo H. N.Passos-Bueno, Maria RitaZatz, Mayana2023-07-29T13:59:32Z2023-07-29T13:59:32Z2022-10-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3389/fimmu.2022.975918Frontiers in Immunology, v. 13.1664-3224http://hdl.handle.net/11449/24899810.3389/fimmu.2022.9759182-s2.0-85141376893Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFrontiers in Immunologyinfo:eu-repo/semantics/openAccess2024-06-24T14:52:03Zoai:repositorio.unesp.br:11449/248998Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:15:04.282064Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
title |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
spellingShingle |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil Castelli, Erick C. [UNESP] COVID-19 HLA human leukocyte antigens immune response major histocompatibility complex (MCH) MUC22 resistant genetic variants SARS-CoV-2 |
title_short |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
title_full |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
title_fullStr |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
title_full_unstemmed |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
title_sort |
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil |
author |
Castelli, Erick C. [UNESP] |
author_facet |
Castelli, Erick C. [UNESP] de Castro, Mateus V. Naslavsky, Michel S. Scliar, Marilia O. Silva, Nayane S. B. [UNESP] Pereira, Raphaela N. [UNESP] Ciriaco, Viviane A. O. [UNESP] Castro, Camila F. B. [UNESP] Mendes-Junior, Celso T. Silveira, Etiele de S. de Oliveira, Iuri M. Antonio, Eduardo C. Vieira, Gustavo F. Meyer, Diogo Nunes, Kelly Matos, Larissa R. B. Silva, Monize V. R. Wang, Jaqueline Y. T. Esposito, Joyce Cória, Vivian R. Magawa, Jhosiene Y. Santos, Keity S. Cunha-Neto, Edecio Kalil, Jorge Bortolin, Raul H. Hirata, Mário Hiroyuki Dell’Aquila, Luiz P. Razuk-Filho, Alvaro Batista-Júnior, Pedro B. Duarte-Neto, Amaro N. Dolhnikoff, Marisa Saldiva, Paulo H. N. Passos-Bueno, Maria Rita Zatz, Mayana |
author_role |
author |
author2 |
de Castro, Mateus V. Naslavsky, Michel S. Scliar, Marilia O. Silva, Nayane S. B. [UNESP] Pereira, Raphaela N. [UNESP] Ciriaco, Viviane A. O. [UNESP] Castro, Camila F. B. [UNESP] Mendes-Junior, Celso T. Silveira, Etiele de S. de Oliveira, Iuri M. Antonio, Eduardo C. Vieira, Gustavo F. Meyer, Diogo Nunes, Kelly Matos, Larissa R. B. Silva, Monize V. R. Wang, Jaqueline Y. T. Esposito, Joyce Cória, Vivian R. Magawa, Jhosiene Y. Santos, Keity S. Cunha-Neto, Edecio Kalil, Jorge Bortolin, Raul H. Hirata, Mário Hiroyuki Dell’Aquila, Luiz P. Razuk-Filho, Alvaro Batista-Júnior, Pedro B. Duarte-Neto, Amaro N. Dolhnikoff, Marisa Saldiva, Paulo H. N. Passos-Bueno, Maria Rita Zatz, Mayana |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade de São Paulo (USP) Centro Universitário Sudoeste Paulista Universidade Federal do Rio Grande do Sul (UFRGS) Universidade La Salle Instituto Nacional de Ciências e Tecnologia-iii (INCT) Prevent Senior Institute |
dc.contributor.author.fl_str_mv |
Castelli, Erick C. [UNESP] de Castro, Mateus V. Naslavsky, Michel S. Scliar, Marilia O. Silva, Nayane S. B. [UNESP] Pereira, Raphaela N. [UNESP] Ciriaco, Viviane A. O. [UNESP] Castro, Camila F. B. [UNESP] Mendes-Junior, Celso T. Silveira, Etiele de S. de Oliveira, Iuri M. Antonio, Eduardo C. Vieira, Gustavo F. Meyer, Diogo Nunes, Kelly Matos, Larissa R. B. Silva, Monize V. R. Wang, Jaqueline Y. T. Esposito, Joyce Cória, Vivian R. Magawa, Jhosiene Y. Santos, Keity S. Cunha-Neto, Edecio Kalil, Jorge Bortolin, Raul H. Hirata, Mário Hiroyuki Dell’Aquila, Luiz P. Razuk-Filho, Alvaro Batista-Júnior, Pedro B. Duarte-Neto, Amaro N. Dolhnikoff, Marisa Saldiva, Paulo H. N. Passos-Bueno, Maria Rita Zatz, Mayana |
dc.subject.por.fl_str_mv |
COVID-19 HLA human leukocyte antigens immune response major histocompatibility complex (MCH) MUC22 resistant genetic variants SARS-CoV-2 |
topic |
COVID-19 HLA human leukocyte antigens immune response major histocompatibility complex (MCH) MUC22 resistant genetic variants SARS-CoV-2 |
description |
Background: 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. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-10-25 2023-07-29T13:59:32Z 2023-07-29T13:59:32Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3389/fimmu.2022.975918 Frontiers in Immunology, v. 13. 1664-3224 http://hdl.handle.net/11449/248998 10.3389/fimmu.2022.975918 2-s2.0-85141376893 |
url |
http://dx.doi.org/10.3389/fimmu.2022.975918 http://hdl.handle.net/11449/248998 |
identifier_str_mv |
Frontiers in Immunology, v. 13. 1664-3224 10.3389/fimmu.2022.975918 2-s2.0-85141376893 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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Frontiers in Immunology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
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UNESP |
reponame_str |
Repositório Institucional da UNESP |
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Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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1808129502058905600 |