Effects of aging on B cell function
Ability to make an optimal immune response to vaccines and infectious agents declines with age in humans and animal models. Recent advances have shown intrinsic B cell defects in aged mice and humans, including decreases in Ig class switch recombination (CSR), activation-induced cytidine deaminase (...
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Veröffentlicht in: | Current opinion in immunology 2009-08, Vol.21 (4), p.425-430 |
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description | Ability to make an optimal immune response to vaccines and infectious agents declines with age in humans and animal models. Recent advances have shown intrinsic B cell defects in aged mice and humans, including decreases in Ig class switch recombination (CSR), activation-induced cytidine deaminase (AID), and E47 transcription factor. Effects on somatic hypermutation (SHM) have been varied depending on the system studied. Increase of AID in mice has shown improved CSR but not SHM. The reported microarray analysis of human B cell subsets may now be used to delineate B cell defects with aging and all the advances presented should lead to selecting agents for improved immune response in the elderly. |
doi_str_mv | 10.1016/j.coi.2009.06.001 |
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Recent advances have shown intrinsic B cell defects in aged mice and humans, including decreases in Ig class switch recombination (CSR), activation-induced cytidine deaminase (AID), and E47 transcription factor. Effects on somatic hypermutation (SHM) have been varied depending on the system studied. Increase of AID in mice has shown improved CSR but not SHM. The reported microarray analysis of human B cell subsets may now be used to delineate B cell defects with aging and all the advances presented should lead to selecting agents for improved immune response in the elderly.</description><identifier>ISSN: 0952-7915</identifier><identifier>ISSN: 1879-0372</identifier><identifier>EISSN: 1879-0372</identifier><identifier>DOI: 10.1016/j.coi.2009.06.001</identifier><identifier>PMID: 19608393</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Aging - immunology ; Aging - metabolism ; Aging - pathology ; Allergy and Immunology ; Animals ; B-Lymphocytes - immunology ; B-Lymphocytes - metabolism ; B-Lymphocytes - pathology ; Cytidine Deaminase - genetics ; Cytidine Deaminase - immunology ; Cytidine Deaminase - metabolism ; Gene Expression Regulation - immunology ; Humans ; Immune Tolerance ; Immunoglobulin Class Switching ; Mice ; Somatic Hypermutation, Immunoglobulin ; TCF Transcription Factors - genetics ; TCF Transcription Factors - immunology ; TCF Transcription Factors - metabolism ; Transcription Factor 7-Like 1 Protein</subject><ispartof>Current opinion in immunology, 2009-08, Vol.21 (4), p.425-430</ispartof><rights>Elsevier Ltd</rights><rights>2009 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-2cae02543a867879e9392e2b8ec5d2c150ee62c5bcd11ebeec8ea94fa916f7fe3</citedby><cites>FETCH-LOGICAL-c536t-2cae02543a867879e9392e2b8ec5d2c150ee62c5bcd11ebeec8ea94fa916f7fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0952791509001319$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19608393$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frasca, Daniela</creatorcontrib><creatorcontrib>Blomberg, Bonnie B</creatorcontrib><title>Effects of aging on B cell function</title><title>Current opinion in immunology</title><addtitle>Curr Opin Immunol</addtitle><description>Ability to make an optimal immune response to vaccines and infectious agents declines with age in humans and animal models. Recent advances have shown intrinsic B cell defects in aged mice and humans, including decreases in Ig class switch recombination (CSR), activation-induced cytidine deaminase (AID), and E47 transcription factor. Effects on somatic hypermutation (SHM) have been varied depending on the system studied. Increase of AID in mice has shown improved CSR but not SHM. The reported microarray analysis of human B cell subsets may now be used to delineate B cell defects with aging and all the advances presented should lead to selecting agents for improved immune response in the elderly.</description><subject>Aging - immunology</subject><subject>Aging - metabolism</subject><subject>Aging - pathology</subject><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - metabolism</subject><subject>B-Lymphocytes - pathology</subject><subject>Cytidine Deaminase - genetics</subject><subject>Cytidine Deaminase - immunology</subject><subject>Cytidine Deaminase - metabolism</subject><subject>Gene Expression Regulation - immunology</subject><subject>Humans</subject><subject>Immune Tolerance</subject><subject>Immunoglobulin Class Switching</subject><subject>Mice</subject><subject>Somatic Hypermutation, Immunoglobulin</subject><subject>TCF Transcription Factors - genetics</subject><subject>TCF Transcription Factors - immunology</subject><subject>TCF Transcription Factors - metabolism</subject><subject>Transcription Factor 7-Like 1 Protein</subject><issn>0952-7915</issn><issn>1879-0372</issn><issn>1879-0372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ks1r3DAQxUVpaTZp_4BeiqHQnuyOpJVsUQikIf2AQA9tz4NWHm219UqpZQfy31dml_TjkJMO-r3HzHvD2AsODQeu3-4al0IjAEwDugHgj9iKd62pQbbiMVuBUaJuDVcn7DTnHQAoJeEpO-FGQyeNXLFXV96Tm3KVfGW3IW6rFKv3laNhqPwc3RRSfMaeeDtken58z9j3D1ffLj_V118-fr68uK6dknqqhbMEQq2l7XRbpiAjjSCx6cipXjiugEgLpzau55w2RK4ja9beGq5960mesfOD78282VPvKE6jHfBmDHs73mGyAf_9ieEHbtMtik5JqdfF4M3RYEy_ZsoT7kNeVrGR0pyxlVK1nRSikK8fJAUILkuIBeQH0I0p55H8_TgccCkBd1hKwKUEBI2lhKJ5-fcefxTH1Avw7gBQSfM20IjZBYqO-jCWMrAvhg_Zn_-ndkOIwdnhJ91R3qV5jKUm5JgFAn5drmA5AjCLmhv5G1vvq9Q</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Frasca, Daniela</creator><creator>Blomberg, Bonnie B</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090801</creationdate><title>Effects of aging on B cell function</title><author>Frasca, Daniela ; Blomberg, Bonnie B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-2cae02543a867879e9392e2b8ec5d2c150ee62c5bcd11ebeec8ea94fa916f7fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aging - immunology</topic><topic>Aging - metabolism</topic><topic>Aging - pathology</topic><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>B-Lymphocytes - immunology</topic><topic>B-Lymphocytes - metabolism</topic><topic>B-Lymphocytes - pathology</topic><topic>Cytidine Deaminase - genetics</topic><topic>Cytidine Deaminase - immunology</topic><topic>Cytidine Deaminase - metabolism</topic><topic>Gene Expression Regulation - immunology</topic><topic>Humans</topic><topic>Immune Tolerance</topic><topic>Immunoglobulin Class Switching</topic><topic>Mice</topic><topic>Somatic Hypermutation, Immunoglobulin</topic><topic>TCF Transcription Factors - genetics</topic><topic>TCF Transcription Factors - immunology</topic><topic>TCF Transcription Factors - metabolism</topic><topic>Transcription Factor 7-Like 1 Protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frasca, Daniela</creatorcontrib><creatorcontrib>Blomberg, Bonnie B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current opinion in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frasca, Daniela</au><au>Blomberg, Bonnie B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of aging on B cell function</atitle><jtitle>Current opinion in immunology</jtitle><addtitle>Curr Opin Immunol</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>21</volume><issue>4</issue><spage>425</spage><epage>430</epage><pages>425-430</pages><issn>0952-7915</issn><issn>1879-0372</issn><eissn>1879-0372</eissn><abstract>Ability to make an optimal immune response to vaccines and infectious agents declines with age in humans and animal models. 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subjects | Aging - immunology Aging - metabolism Aging - pathology Allergy and Immunology Animals B-Lymphocytes - immunology B-Lymphocytes - metabolism B-Lymphocytes - pathology Cytidine Deaminase - genetics Cytidine Deaminase - immunology Cytidine Deaminase - metabolism Gene Expression Regulation - immunology Humans Immune Tolerance Immunoglobulin Class Switching Mice Somatic Hypermutation, Immunoglobulin TCF Transcription Factors - genetics TCF Transcription Factors - immunology TCF Transcription Factors - metabolism Transcription Factor 7-Like 1 Protein |
title | Effects of aging on B cell function |
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