CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.6/11184 |
Resumo: | There is increasing evidence that in humans the adaptive immunological system can influence cognitive functions of the brain. We have undertaken a comprehensive immunological analysis of lymphocyte and monocyte populations as well as of HLA molecules expression in a cohort of elderly volunteers (age range, 64-101) differing in their cognitive status. Hereby, we report on the identification of a novel signature in cognitively impaired elderly characterized by: (1) elevated percentages of CD8+ T effector-memory cells expressing high levels of the CD45RA phosphate receptor (Temra hi); (2) high percentages of CD8+ T cells expressing high levels of the CD8β chain (CD8βhi); (3) augmented production of IFNγ by in vitro activated CD4+ T cells. Noteworthy, CD3+CD8+ Temra hi and CD3+CD8βhi cells were associated with impaired cognition. Cytomegalovirus seroprevalence showed that all volunteers studied but one were CMV positive. Finally, we show that some of these phenotypic and functional features are associated with an increased frequency of the HLA-B8 serotype, which belongs to the ancestral haplotype HLA-A1, Cw7, B8, DR3, DQ2, among cognitively impaired volunteers. To our knowledge, this is the first proof in humans linking the amount of cell surface CD45RA and CD8β chain expressed by CD8+ Temra cells, and the amount of IFNγ produced by in vitro activated CD4+ T cells, with impaired cognitive function in the elderly. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive FunctionCD8 AntigensCD8-Positive T-LymphocytesCognitive DysfunctionHumansImmunophenotypingInterferon-gammaLeukocyte Common AntigensLeukocytes, MononuclearLymphocyte ActivationPrevalenceT-Lymphocyte SubsetsBiomarkersCognitionThere is increasing evidence that in humans the adaptive immunological system can influence cognitive functions of the brain. We have undertaken a comprehensive immunological analysis of lymphocyte and monocyte populations as well as of HLA molecules expression in a cohort of elderly volunteers (age range, 64-101) differing in their cognitive status. Hereby, we report on the identification of a novel signature in cognitively impaired elderly characterized by: (1) elevated percentages of CD8+ T effector-memory cells expressing high levels of the CD45RA phosphate receptor (Temra hi); (2) high percentages of CD8+ T cells expressing high levels of the CD8β chain (CD8βhi); (3) augmented production of IFNγ by in vitro activated CD4+ T cells. Noteworthy, CD3+CD8+ Temra hi and CD3+CD8βhi cells were associated with impaired cognition. Cytomegalovirus seroprevalence showed that all volunteers studied but one were CMV positive. Finally, we show that some of these phenotypic and functional features are associated with an increased frequency of the HLA-B8 serotype, which belongs to the ancestral haplotype HLA-A1, Cw7, B8, DR3, DQ2, among cognitively impaired volunteers. To our knowledge, this is the first proof in humans linking the amount of cell surface CD45RA and CD8β chain expressed by CD8+ Temra cells, and the amount of IFNγ produced by in vitro activated CD4+ T cells, with impaired cognitive function in the elderly.uBibliorumEsgalhado, AJReste-Ferreira, DéboraAlbino, StephanieSousa, AdrianaAmaral, Ana PaulaMartinho, AntónioOliveira, Isabel TomásVerde, IgnacioLourenço, OlgaFonseca, Ana MCardoso, Elsa M.Arosa, FA2021-07-05T10:11:52Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.6/11184eng10.3389/fimmu.2020.592656info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-11-27T12:36:02Zoai:ubibliorum.ubi.pt:10400.6/11184Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-11-27T12:36:02Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
title |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
spellingShingle |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function Esgalhado, AJ CD8 Antigens CD8-Positive T-Lymphocytes Cognitive Dysfunction Humans Immunophenotyping Interferon-gamma Leukocyte Common Antigens Leukocytes, Mononuclear Lymphocyte Activation Prevalence T-Lymphocyte Subsets Biomarkers Cognition |
title_short |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
title_full |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
title_fullStr |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
title_full_unstemmed |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
title_sort |
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function |
author |
Esgalhado, AJ |
author_facet |
Esgalhado, AJ Reste-Ferreira, Débora Albino, Stephanie Sousa, Adriana Amaral, Ana Paula Martinho, António Oliveira, Isabel Tomás Verde, Ignacio Lourenço, Olga Fonseca, Ana M Cardoso, Elsa M. Arosa, FA |
author_role |
author |
author2 |
Reste-Ferreira, Débora Albino, Stephanie Sousa, Adriana Amaral, Ana Paula Martinho, António Oliveira, Isabel Tomás Verde, Ignacio Lourenço, Olga Fonseca, Ana M Cardoso, Elsa M. Arosa, FA |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
uBibliorum |
dc.contributor.author.fl_str_mv |
Esgalhado, AJ Reste-Ferreira, Débora Albino, Stephanie Sousa, Adriana Amaral, Ana Paula Martinho, António Oliveira, Isabel Tomás Verde, Ignacio Lourenço, Olga Fonseca, Ana M Cardoso, Elsa M. Arosa, FA |
dc.subject.por.fl_str_mv |
CD8 Antigens CD8-Positive T-Lymphocytes Cognitive Dysfunction Humans Immunophenotyping Interferon-gamma Leukocyte Common Antigens Leukocytes, Mononuclear Lymphocyte Activation Prevalence T-Lymphocyte Subsets Biomarkers Cognition |
topic |
CD8 Antigens CD8-Positive T-Lymphocytes Cognitive Dysfunction Humans Immunophenotyping Interferon-gamma Leukocyte Common Antigens Leukocytes, Mononuclear Lymphocyte Activation Prevalence T-Lymphocyte Subsets Biomarkers Cognition |
description |
There is increasing evidence that in humans the adaptive immunological system can influence cognitive functions of the brain. We have undertaken a comprehensive immunological analysis of lymphocyte and monocyte populations as well as of HLA molecules expression in a cohort of elderly volunteers (age range, 64-101) differing in their cognitive status. Hereby, we report on the identification of a novel signature in cognitively impaired elderly characterized by: (1) elevated percentages of CD8+ T effector-memory cells expressing high levels of the CD45RA phosphate receptor (Temra hi); (2) high percentages of CD8+ T cells expressing high levels of the CD8β chain (CD8βhi); (3) augmented production of IFNγ by in vitro activated CD4+ T cells. Noteworthy, CD3+CD8+ Temra hi and CD3+CD8βhi cells were associated with impaired cognition. Cytomegalovirus seroprevalence showed that all volunteers studied but one were CMV positive. Finally, we show that some of these phenotypic and functional features are associated with an increased frequency of the HLA-B8 serotype, which belongs to the ancestral haplotype HLA-A1, Cw7, B8, DR3, DQ2, among cognitively impaired volunteers. To our knowledge, this is the first proof in humans linking the amount of cell surface CD45RA and CD8β chain expressed by CD8+ Temra cells, and the amount of IFNγ produced by in vitro activated CD4+ T cells, with impaired cognitive function in the elderly. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 2020-01-01T00:00:00Z 2021-07-05T10:11:52Z |
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://hdl.handle.net/10400.6/11184 |
url |
http://hdl.handle.net/10400.6/11184 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.3389/fimmu.2020.592656 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817549656529305600 |