A prospective study of in vitro anti-HBs producing B cells (spot-ELISA) following primary and supplementary vaccination with a recombinant hepatitis B vaccine in insulin dependent diabetic patients and matched controls
A prospective study of the immune response after hepatitis B vaccination was carried out in 32 insulin dependent diabetes mellitus (IDDM) patients and their age and sex matched healthy controls. A sensitive, immunoenzymatic technique was used, able to detect in vitro specific antibody production by...
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Veröffentlicht in: | Journal of medical virology 1991-11, Vol.35 (3), p.216-222 |
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creator | Wismans, P. J. Van Hattum, J. De Gast, G. C. Bouter, K. P. Diepersloot, R. J. A. Maikoe, T. J. Mudde, G. C. |
description | A prospective study of the immune response after hepatitis B vaccination was carried out in 32 insulin dependent diabetes mellitus (IDDM) patients and their age and sex matched healthy controls. A sensitive, immunoenzymatic technique was used, able to detect in vitro specific antibody production by mitogen stimulated individual B cells.
In‐vivo serologic response after vaccinationwith a standard scheme (0, 1 and 6 months) of 20 pg recombinant hepatitis B (HB) vaccine was significantly impaired in the IDDM patients both with respect to the number of nonresponders (25 versus 3%, P < 0.05) and antibody titers reached (1,377 vs. 9,060 IU/L, P < 0.05). The total number of in vitro IgM‐ and IgG‐class immunoglobulin producing B cells as detected by the spot‐ELISA, was found to be comparable in both groups. Specific IgG anti‐HBs (and to a lesser extent IgM anti‐HBs) showed impairment in the diabetic population as a whole. The number of IgG anti‐HBs producing B cells was mark‐ edly depressed one month following vaccination, which is probably a reflection of homing of B cells outside the circulation.
Responding subjects were identified early during their vaccination by the detection of in vitro anti‐HBs production using the spot‐ELISA. Nonresponding healthy subjects and IDDM patients as a group showed a low number of IgG anti‐HBs spots, suggesting a reduced specific memory B cell frequency. In 13 of 15 hypo‐ and nonresponders with positive IgG anti‐HBs spots supplementary vaccination(s) resulted in improved anti‐HBs levels. |
doi_str_mv | 10.1002/jmv.1890350313 |
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In‐vivo serologic response after vaccinationwith a standard scheme (0, 1 and 6 months) of 20 pg recombinant hepatitis B (HB) vaccine was significantly impaired in the IDDM patients both with respect to the number of nonresponders (25 versus 3%, P < 0.05) and antibody titers reached (1,377 vs. 9,060 IU/L, P < 0.05). The total number of in vitro IgM‐ and IgG‐class immunoglobulin producing B cells as detected by the spot‐ELISA, was found to be comparable in both groups. Specific IgG anti‐HBs (and to a lesser extent IgM anti‐HBs) showed impairment in the diabetic population as a whole. The number of IgG anti‐HBs producing B cells was mark‐ edly depressed one month following vaccination, which is probably a reflection of homing of B cells outside the circulation.
Responding subjects were identified early during their vaccination by the detection of in vitro anti‐HBs production using the spot‐ELISA. Nonresponding healthy subjects and IDDM patients as a group showed a low number of IgG anti‐HBs spots, suggesting a reduced specific memory B cell frequency. In 13 of 15 hypo‐ and nonresponders with positive IgG anti‐HBs spots supplementary vaccination(s) resulted in improved anti‐HBs levels.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.1890350313</identifier><identifier>PMID: 1839554</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; antigens ; B-Lymphocytes - immunology ; Biological and medical sciences ; Diabetes Mellitus, Type 1 - immunology ; Enzyme-Linked Immunosorbent Assay ; Female ; hepatitis B antibodies ; Hepatitis B Antibodies - biosynthesis ; hepatitis B antigens ; Hepatitis B Vaccines ; Human viral diseases ; Humans ; immune response ; Immunization ; In Vitro Techniques ; Infectious diseases ; insulin dependent diabetes mellitus ; Male ; Medical sciences ; Middle Aged ; Prospective Studies ; Vaccines, Synthetic - administration & dosage ; Viral diseases ; Viral hepatitis ; viral hepatitis vaccines ; Viral Hepatitis Vaccines - administration & dosage</subject><ispartof>Journal of medical virology, 1991-11, Vol.35 (3), p.216-222</ispartof><rights>Copyright © 1991 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3533-dd9b3ce1da63f6267e003a14bdadec5b27b6bf2f409cabab26ad30806b24bbdc3</citedby><cites>FETCH-LOGICAL-c3533-dd9b3ce1da63f6267e003a14bdadec5b27b6bf2f409cabab26ad30806b24bbdc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.1890350313$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.1890350313$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5146032$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1839554$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wismans, P. J.</creatorcontrib><creatorcontrib>Van Hattum, J.</creatorcontrib><creatorcontrib>De Gast, G. C.</creatorcontrib><creatorcontrib>Bouter, K. P.</creatorcontrib><creatorcontrib>Diepersloot, R. J. A.</creatorcontrib><creatorcontrib>Maikoe, T. J.</creatorcontrib><creatorcontrib>Mudde, G. C.</creatorcontrib><title>A prospective study of in vitro anti-HBs producing B cells (spot-ELISA) following primary and supplementary vaccination with a recombinant hepatitis B vaccine in insulin dependent diabetic patients and matched controls</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>A prospective study of the immune response after hepatitis B vaccination was carried out in 32 insulin dependent diabetes mellitus (IDDM) patients and their age and sex matched healthy controls. A sensitive, immunoenzymatic technique was used, able to detect in vitro specific antibody production by mitogen stimulated individual B cells.
In‐vivo serologic response after vaccinationwith a standard scheme (0, 1 and 6 months) of 20 pg recombinant hepatitis B (HB) vaccine was significantly impaired in the IDDM patients both with respect to the number of nonresponders (25 versus 3%, P < 0.05) and antibody titers reached (1,377 vs. 9,060 IU/L, P < 0.05). The total number of in vitro IgM‐ and IgG‐class immunoglobulin producing B cells as detected by the spot‐ELISA, was found to be comparable in both groups. Specific IgG anti‐HBs (and to a lesser extent IgM anti‐HBs) showed impairment in the diabetic population as a whole. The number of IgG anti‐HBs producing B cells was mark‐ edly depressed one month following vaccination, which is probably a reflection of homing of B cells outside the circulation.
Responding subjects were identified early during their vaccination by the detection of in vitro anti‐HBs production using the spot‐ELISA. Nonresponding healthy subjects and IDDM patients as a group showed a low number of IgG anti‐HBs spots, suggesting a reduced specific memory B cell frequency. In 13 of 15 hypo‐ and nonresponders with positive IgG anti‐HBs spots supplementary vaccination(s) resulted in improved anti‐HBs levels.</description><subject>Adult</subject><subject>antigens</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>hepatitis B antibodies</subject><subject>Hepatitis B Antibodies - biosynthesis</subject><subject>hepatitis B antigens</subject><subject>Hepatitis B Vaccines</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>immune response</subject><subject>Immunization</subject><subject>In Vitro Techniques</subject><subject>Infectious diseases</subject><subject>insulin dependent diabetes mellitus</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Vaccines, Synthetic - administration & dosage</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>viral hepatitis vaccines</subject><subject>Viral Hepatitis Vaccines - administration & dosage</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhiMEKkvLlRuSD6iCQ7Z2nDjJcVt1t4Wllfg8Wv6YsC6JE2Jnl_2r_BocsmrFqSdLM8_7zmheR9ErgucE4-TsrtnOSVFimmFK6JNoRnDJ4hLn5Gk0wyRlMWMkex69cO4OY1yUSXIUHZGCllmWzqI_C9T1retAebMF5Pyg96itkLFoa3zfImG9ia_O3YjpQRn7A50jBXXt0FvXtT6-XF9_XrxDVVvX7W5sd71pRL8PSo3c0HU1NGD9WNkKFQyEN61FO-M3SKAeVNvIULQebaALPW9cmDChMO5hrBvq8GrowOpghbQRErxRaORDwf2b1QivNqCRam1YvHYn0bNK1A5eHt7j6Ovy8svFVby-XV1fLNaxohmlsdalpAqIFoxWLGE5YEwFSaUWGlQmk1wyWSVVikslpJAJE5riAjOZpFJqRY-j08k3XOjXAM7zxrjxQsJCOzieJ6woSMkeBQlL07Qo0wDOJ1CFaFwPFT_clBPMx9R5SJ0_pB4Erw_Og2xAP-BTzKH_5tAXTom66oVVxt1jWfgmmCYBKydsZ2rYPzKUv__47b8V4klrnIff91rR_-Qsp3nGv9-seLFarj99WDKe0b_-VNsN</recordid><startdate>199111</startdate><enddate>199111</enddate><creator>Wismans, P. J.</creator><creator>Van Hattum, J.</creator><creator>De Gast, G. C.</creator><creator>Bouter, K. P.</creator><creator>Diepersloot, R. J. A.</creator><creator>Maikoe, T. J.</creator><creator>Mudde, G. C.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199111</creationdate><title>A prospective study of in vitro anti-HBs producing B cells (spot-ELISA) following primary and supplementary vaccination with a recombinant hepatitis B vaccine in insulin dependent diabetic patients and matched controls</title><author>Wismans, P. J. ; Van Hattum, J. ; De Gast, G. C. ; Bouter, K. P. ; Diepersloot, R. J. A. ; Maikoe, T. J. ; Mudde, G. C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3533-dd9b3ce1da63f6267e003a14bdadec5b27b6bf2f409cabab26ad30806b24bbdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adult</topic><topic>antigens</topic><topic>B-Lymphocytes - immunology</topic><topic>Biological and medical sciences</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>hepatitis B antibodies</topic><topic>Hepatitis B Antibodies - biosynthesis</topic><topic>hepatitis B antigens</topic><topic>Hepatitis B Vaccines</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>immune response</topic><topic>Immunization</topic><topic>In Vitro Techniques</topic><topic>Infectious diseases</topic><topic>insulin dependent diabetes mellitus</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Vaccines, Synthetic - administration & dosage</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>viral hepatitis vaccines</topic><topic>Viral Hepatitis Vaccines - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wismans, P. J.</creatorcontrib><creatorcontrib>Van Hattum, J.</creatorcontrib><creatorcontrib>De Gast, G. C.</creatorcontrib><creatorcontrib>Bouter, K. P.</creatorcontrib><creatorcontrib>Diepersloot, R. J. A.</creatorcontrib><creatorcontrib>Maikoe, T. J.</creatorcontrib><creatorcontrib>Mudde, G. C.</creatorcontrib><collection>Istex</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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wismans, P. J.</au><au>Van Hattum, J.</au><au>De Gast, G. C.</au><au>Bouter, K. P.</au><au>Diepersloot, R. J. A.</au><au>Maikoe, T. J.</au><au>Mudde, G. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A prospective study of in vitro anti-HBs producing B cells (spot-ELISA) following primary and supplementary vaccination with a recombinant hepatitis B vaccine in insulin dependent diabetic patients and matched controls</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>1991-11</date><risdate>1991</risdate><volume>35</volume><issue>3</issue><spage>216</spage><epage>222</epage><pages>216-222</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>A prospective study of the immune response after hepatitis B vaccination was carried out in 32 insulin dependent diabetes mellitus (IDDM) patients and their age and sex matched healthy controls. A sensitive, immunoenzymatic technique was used, able to detect in vitro specific antibody production by mitogen stimulated individual B cells.
In‐vivo serologic response after vaccinationwith a standard scheme (0, 1 and 6 months) of 20 pg recombinant hepatitis B (HB) vaccine was significantly impaired in the IDDM patients both with respect to the number of nonresponders (25 versus 3%, P < 0.05) and antibody titers reached (1,377 vs. 9,060 IU/L, P < 0.05). The total number of in vitro IgM‐ and IgG‐class immunoglobulin producing B cells as detected by the spot‐ELISA, was found to be comparable in both groups. Specific IgG anti‐HBs (and to a lesser extent IgM anti‐HBs) showed impairment in the diabetic population as a whole. The number of IgG anti‐HBs producing B cells was mark‐ edly depressed one month following vaccination, which is probably a reflection of homing of B cells outside the circulation.
Responding subjects were identified early during their vaccination by the detection of in vitro anti‐HBs production using the spot‐ELISA. Nonresponding healthy subjects and IDDM patients as a group showed a low number of IgG anti‐HBs spots, suggesting a reduced specific memory B cell frequency. In 13 of 15 hypo‐ and nonresponders with positive IgG anti‐HBs spots supplementary vaccination(s) resulted in improved anti‐HBs levels.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1839554</pmid><doi>10.1002/jmv.1890350313</doi><tpages>7</tpages></addata></record> |
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subjects | Adult antigens B-Lymphocytes - immunology Biological and medical sciences Diabetes Mellitus, Type 1 - immunology Enzyme-Linked Immunosorbent Assay Female hepatitis B antibodies Hepatitis B Antibodies - biosynthesis hepatitis B antigens Hepatitis B Vaccines Human viral diseases Humans immune response Immunization In Vitro Techniques Infectious diseases insulin dependent diabetes mellitus Male Medical sciences Middle Aged Prospective Studies Vaccines, Synthetic - administration & dosage Viral diseases Viral hepatitis viral hepatitis vaccines Viral Hepatitis Vaccines - administration & dosage |
title | A prospective study of in vitro anti-HBs producing B cells (spot-ELISA) following primary and supplementary vaccination with a recombinant hepatitis B vaccine in insulin dependent diabetic patients and matched controls |
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