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Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults
Although pituitary hormones are known to affect immune function, treated hypopituitarism is not a recognized cause of immune deficiency in humans. We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1),...
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Published in: | Clinical and experimental immunology 2009-05, Vol.156 (2), p.271-277 |
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description | Although pituitary hormones are known to affect immune function, treated hypopituitarism is not a recognized cause of immune deficiency in humans. We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1), on stable pituitary replacement including growth hormone, and 12 healthy volunteers (group 2) were studied. Lymphocyte subsets, pneumococcal antibody levels pre- and 1 month after polysaccharide vaccination, T cell numbers and in-vitro interferon (IFN)-γ response were studied. There were no significant differences in T cell numbers or IFN-γ secretion. B cell numbers were lower in group 1, especially those with low prolactin levels. Independent of this finding, nine of 21 patients in this group had low antibody response to polysaccharide antigen. This was most striking in those with low insulin-like growth factor 1 levels and appeared to be independent of the use of anti-convulsants or corticosteroid replacement. Significant humoral immune deficiency is seen in panhypopituitarism and may contribute to morbidity. |
doi_str_mv | 10.1111/j.1365-2249.2009.03881.x |
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We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1), on stable pituitary replacement including growth hormone, and 12 healthy volunteers (group 2) were studied. Lymphocyte subsets, pneumococcal antibody levels pre- and 1 month after polysaccharide vaccination, T cell numbers and in-vitro interferon (IFN)-γ response were studied. There were no significant differences in T cell numbers or IFN-γ secretion. B cell numbers were lower in group 1, especially those with low prolactin levels. Independent of this finding, nine of 21 patients in this group had low antibody response to polysaccharide antigen. This was most striking in those with low insulin-like growth factor 1 levels and appeared to be independent of the use of anti-convulsants or corticosteroid replacement. Significant humoral immune deficiency is seen in panhypopituitarism and may contribute to morbidity.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/j.1365-2249.2009.03881.x</identifier><identifier>PMID: 19236430</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Analytical, structural and metabolic biochemistry ; Antibodies, Bacterial - blood ; Antibody Formation ; autoimmunity ; Biological and medical sciences ; Case-Control Studies ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. Psychology ; Human Growth Hormone - therapeutic use ; Humans ; hypopituitarism ; Hypopituitarism - blood ; Hypopituitarism - drug therapy ; Hypopituitarism - immunology ; Hypothalamus. Hypophysis. Epiphysis (diseases) ; immune function ; Immunoglobulin G - blood ; Insulin-Like Growth Factor I - analysis ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; Non tumoral diseases. Target tissue resistance. Benign neoplasms ; Pneumococcal Vaccines - administration & dosage ; Pneumococcal Vaccines - immunology ; Prolactin - blood ; prolactin deficiency ; Streptococcus pneumoniae ; T-Lymphocyte Subsets - immunology ; Tetanus Toxoid - immunology ; Translational Studies ; Vaccination</subject><ispartof>Clinical and experimental immunology, 2009-05, Vol.156 (2), p.271-277</ispartof><rights>2009 British Society for Immunology</rights><rights>2009 INIST-CNRS</rights><rights>Journal Compilation © 2009 British Society for Immunology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5571-2466d192b7ee8fd1a623c59ce75736e92fceff556f1739ba560782db98a1d0ed3</citedby><cites>FETCH-LOGICAL-c5571-2466d192b7ee8fd1a623c59ce75736e92fceff556f1739ba560782db98a1d0ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759475/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759475/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21336130$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19236430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukherjee, A</creatorcontrib><creatorcontrib>Helbert, M</creatorcontrib><creatorcontrib>Ryder, W.D.J</creatorcontrib><creatorcontrib>Borrow, R</creatorcontrib><creatorcontrib>Davis, J.R.E</creatorcontrib><creatorcontrib>Shalet, S.M</creatorcontrib><title>Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>Although pituitary hormones are known to affect immune function, treated hypopituitarism is not a recognized cause of immune deficiency in humans. We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1), on stable pituitary replacement including growth hormone, and 12 healthy volunteers (group 2) were studied. Lymphocyte subsets, pneumococcal antibody levels pre- and 1 month after polysaccharide vaccination, T cell numbers and in-vitro interferon (IFN)-γ response were studied. There were no significant differences in T cell numbers or IFN-γ secretion. B cell numbers were lower in group 1, especially those with low prolactin levels. Independent of this finding, nine of 21 patients in this group had low antibody response to polysaccharide antigen. This was most striking in those with low insulin-like growth factor 1 levels and appeared to be independent of the use of anti-convulsants or corticosteroid replacement. Significant humoral immune deficiency is seen in panhypopituitarism and may contribute to morbidity.</description><subject>Adult</subject><subject>Aged</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antibody Formation</subject><subject>autoimmunity</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Human Growth Hormone - therapeutic use</subject><subject>Humans</subject><subject>hypopituitarism</subject><subject>Hypopituitarism - blood</subject><subject>Hypopituitarism - drug therapy</subject><subject>Hypopituitarism - immunology</subject><subject>Hypothalamus. Hypophysis. Epiphysis (diseases)</subject><subject>immune function</subject><subject>Immunoglobulin G - blood</subject><subject>Insulin-Like Growth Factor I - analysis</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Non tumoral diseases. Target tissue resistance. Benign neoplasms</subject><subject>Pneumococcal Vaccines - administration & dosage</subject><subject>Pneumococcal Vaccines - immunology</subject><subject>Prolactin - blood</subject><subject>prolactin deficiency</subject><subject>Streptococcus pneumoniae</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>Tetanus Toxoid - immunology</subject><subject>Translational Studies</subject><subject>Vaccination</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkUuP0zAUhS0EYsrAX4BsYJfgR2wnC5BQNS9pJBYwC1aW41y3rtI42AlM_j1OWxVYgTe2db9zfKyDUEZwQdJ6vysIEzyntKwLinFdYFZVpHh8glbnwVO0wmmU1wSXF-hFjLt0FULQ5-iC1JSJkuEV-natXTcFyLzNdD-6xrdzFiAOvo-QjT4bfDdHbcxWB9fCgdlAn7k-GwPoEdps0P12HvzgxsmNOsyZbqdujC_RM6u7CK9O-yV6uL76ur7N7z_f3K0_3eeGc0lyWgrRpjyNBKhsS7SgzPDagOSSCaipNWAt58ISyepGc4FlRdumrjRpMbTsEn08-g5Ts4fWQD8G3akhuH0Ko7x26u9J77Zq438oKnldSp4M3p0Mgv8-QRzV3kUDXad78FNUQhKOSyn-CVLMpaSCJbA6gib4GAPYcxqC1VKg2qmlJ7X0pJYC1aFA9Zikr__8zW_hqbEEvD0BOhrd2aB74-KZo4QxQQ7chyP303Uw_3cAtb66W05J_-aot9orvQnpjYcvFCdrIoigpWS_AGWswlU</recordid><startdate>200905</startdate><enddate>200905</enddate><creator>Mukherjee, A</creator><creator>Helbert, M</creator><creator>Ryder, W.D.J</creator><creator>Borrow, R</creator><creator>Davis, J.R.E</creator><creator>Shalet, S.M</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Blackwell Science Inc</general><scope>FBQ</scope><scope>IQODW</scope><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>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200905</creationdate><title>Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults</title><author>Mukherjee, A ; Helbert, M ; Ryder, W.D.J ; Borrow, R ; Davis, J.R.E ; Shalet, S.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5571-2466d192b7ee8fd1a623c59ce75736e92fceff556f1739ba560782db98a1d0ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Antibodies, Bacterial - blood</topic><topic>Antibody Formation</topic><topic>autoimmunity</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Human Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>hypopituitarism</topic><topic>Hypopituitarism - blood</topic><topic>Hypopituitarism - drug therapy</topic><topic>Hypopituitarism - immunology</topic><topic>Hypothalamus. Hypophysis. Epiphysis (diseases)</topic><topic>immune function</topic><topic>Immunoglobulin G - blood</topic><topic>Insulin-Like Growth Factor I - analysis</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Non tumoral diseases. Target tissue resistance. Benign neoplasms</topic><topic>Pneumococcal Vaccines - administration & dosage</topic><topic>Pneumococcal Vaccines - immunology</topic><topic>Prolactin - blood</topic><topic>prolactin deficiency</topic><topic>Streptococcus pneumoniae</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>Tetanus Toxoid - immunology</topic><topic>Translational Studies</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukherjee, A</creatorcontrib><creatorcontrib>Helbert, M</creatorcontrib><creatorcontrib>Ryder, W.D.J</creatorcontrib><creatorcontrib>Borrow, R</creatorcontrib><creatorcontrib>Davis, J.R.E</creatorcontrib><creatorcontrib>Shalet, S.M</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukherjee, A</au><au>Helbert, M</au><au>Ryder, W.D.J</au><au>Borrow, R</au><au>Davis, J.R.E</au><au>Shalet, S.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2009-05</date><risdate>2009</risdate><volume>156</volume><issue>2</issue><spage>271</spage><epage>277</epage><pages>271-277</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>Although pituitary hormones are known to affect immune function, treated hypopituitarism is not a recognized cause of immune deficiency in humans. We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1), on stable pituitary replacement including growth hormone, and 12 healthy volunteers (group 2) were studied. Lymphocyte subsets, pneumococcal antibody levels pre- and 1 month after polysaccharide vaccination, T cell numbers and in-vitro interferon (IFN)-γ response were studied. There were no significant differences in T cell numbers or IFN-γ secretion. B cell numbers were lower in group 1, especially those with low prolactin levels. Independent of this finding, nine of 21 patients in this group had low antibody response to polysaccharide antigen. This was most striking in those with low insulin-like growth factor 1 levels and appeared to be independent of the use of anti-convulsants or corticosteroid replacement. Significant humoral immune deficiency is seen in panhypopituitarism and may contribute to morbidity.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>19236430</pmid><doi>10.1111/j.1365-2249.2009.03881.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Analytical, structural and metabolic biochemistry Antibodies, Bacterial - blood Antibody Formation autoimmunity Biological and medical sciences Case-Control Studies Endocrinopathies Female Fundamental and applied biological sciences. Psychology Human Growth Hormone - therapeutic use Humans hypopituitarism Hypopituitarism - blood Hypopituitarism - drug therapy Hypopituitarism - immunology Hypothalamus. Hypophysis. Epiphysis (diseases) immune function Immunoglobulin G - blood Insulin-Like Growth Factor I - analysis Logistic Models Male Medical sciences Middle Aged Non tumoral diseases. Target tissue resistance. Benign neoplasms Pneumococcal Vaccines - administration & dosage Pneumococcal Vaccines - immunology Prolactin - blood prolactin deficiency Streptococcus pneumoniae T-Lymphocyte Subsets - immunology Tetanus Toxoid - immunology Translational Studies Vaccination |
title | Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults |
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