CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function

Detalhes bibliográficos
Autor(a) principal: Esgalhado, AJ
Data de Publicação: 2020
Outros Autores: 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
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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spelling 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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