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Older Human B Cells and Antibodies
B cells have a number of different roles in the immune response. Their excellent antigen presentation potential can contribute to the activation of other cells of the immune system, and evidence is emerging that specialized subsets of these cells, that may be increased with age, can influence the ce...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121151/ http://dx.doi.org/10.1007/978-3-319-99375-1_21 |
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author | Dunn-Walters, Deborah K. O’Hare, Joselli Silva |
author_facet | Dunn-Walters, Deborah K. O’Hare, Joselli Silva |
author_sort | Dunn-Walters, Deborah K. |
collection | PubMed |
description | B cells have a number of different roles in the immune response. Their excellent antigen presentation potential can contribute to the activation of other cells of the immune system, and evidence is emerging that specialized subsets of these cells, that may be increased with age, can influence the cell-mediated immune system in antitumor responses. They can also regulate immune responses, to avoid autoreactivity and excessive inflammation. Deficiencies in regulatory B cells may be beneficial in cancer but will only exacerbate the inflammatory environment that is a hallmark of aging. The B cell role as antibody producers is particularly important, since antibodies perform numerous different functions in different environments. Although studying tissue responses in humans is not as easy as in mice, we do know that certain classes of antibodies are more suited to protecting the mucosal tissues (IgA) or responding to T-independent bacterial polysaccharide antigens (IgG(2)) so we can make some inference with respect to tissue-specific immunity from a study of peripheral blood. We can also make inferences about changes in B cell development with age by looking at the repertoire of different B cell populations to see how age affects the selection events that would normally occur to avoid autoreactivity, or increase specificity, to antigen. |
format | Online Article Text |
id | pubmed-7121151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71211512020-04-06 Older Human B Cells and Antibodies Dunn-Walters, Deborah K. O’Hare, Joselli Silva Handbook of Immunosenescence Article B cells have a number of different roles in the immune response. Their excellent antigen presentation potential can contribute to the activation of other cells of the immune system, and evidence is emerging that specialized subsets of these cells, that may be increased with age, can influence the cell-mediated immune system in antitumor responses. They can also regulate immune responses, to avoid autoreactivity and excessive inflammation. Deficiencies in regulatory B cells may be beneficial in cancer but will only exacerbate the inflammatory environment that is a hallmark of aging. The B cell role as antibody producers is particularly important, since antibodies perform numerous different functions in different environments. Although studying tissue responses in humans is not as easy as in mice, we do know that certain classes of antibodies are more suited to protecting the mucosal tissues (IgA) or responding to T-independent bacterial polysaccharide antigens (IgG(2)) so we can make some inference with respect to tissue-specific immunity from a study of peripheral blood. We can also make inferences about changes in B cell development with age by looking at the repertoire of different B cell populations to see how age affects the selection events that would normally occur to avoid autoreactivity, or increase specificity, to antigen. 2019-04-11 /pmc/articles/PMC7121151/ http://dx.doi.org/10.1007/978-3-319-99375-1_21 Text en © Springer Nature Switzerland AG 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Dunn-Walters, Deborah K. O’Hare, Joselli Silva Older Human B Cells and Antibodies |
title | Older Human B Cells and Antibodies |
title_full | Older Human B Cells and Antibodies |
title_fullStr | Older Human B Cells and Antibodies |
title_full_unstemmed | Older Human B Cells and Antibodies |
title_short | Older Human B Cells and Antibodies |
title_sort | older human b cells and antibodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121151/ http://dx.doi.org/10.1007/978-3-319-99375-1_21 |
work_keys_str_mv | AT dunnwaltersdeborahk olderhumanbcellsandantibodies AT oharejosellisilva olderhumanbcellsandantibodies |