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B Cell Immunosenescence.
Frasca, Daniela; Diaz, Alain; Romero, Maria; Garcia, Denisse; Blomberg, Bonnie B.
Afiliação
  • Frasca D; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, Florida 33136, USA; email: dfrasca@med.miami.edu.
  • Diaz A; Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
  • Romero M; Miami Integrative Metabolomics Research Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
  • Garcia D; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, Florida 33136, USA; email: dfrasca@med.miami.edu.
  • Blomberg BB; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, Florida 33136, USA; email: dfrasca@med.miami.edu.
Annu Rev Cell Dev Biol ; 36: 551-574, 2020 10 06.
Article em En | MEDLINE | ID: mdl-33021823
ABSTRACT
Innate and adaptive immune responses decline with age, leading to greater susceptibility to infectious diseases and reduced responses to vaccines. Diseases are more severe in old than in young individuals and have a greater impact on health outcomes such as morbidity, disability, and mortality. Aging is characterized by increased low-grade chronic inflammation, so-called inflammaging, that represents a link between changes in immune cells and a number of diseases and syndromes typical of old age. In this review we summarize current knowledge on age-associated changes in immune cells with special emphasis on B cells, which are more inflammatory and less responsive to infections and vaccines in the elderly. We highlight recent findings on factors and pathways contributing to inflammaging and how these lead to dysfunctional immune responses. We summarize recent published studies showing that adipose tissue, which increases in size with aging, contributes to inflammaging and dysregulated B cell function.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Imunossenescência Limite: Animals / Humans Idioma: En Revista: Annu Rev Cell Dev Biol Assunto da revista: BIOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Imunossenescência Limite: Animals / Humans Idioma: En Revista: Annu Rev Cell Dev Biol Assunto da revista: BIOLOGIA Ano de publicação: 2020 Tipo de documento: Article