Efficacy of High-Dose Intra-dermal Hepatitis B Virus Vaccine in Previous Vaccination Non-responders with Chronic Liver Disease
Background Hepatitis B virus (HBV) vaccination is essential in chronic liver disease (CLD), because it can help prevent acute-on-chronic disease, which has potentially fatal complications. Unfortunately, this group has a significant proportion of HBV vaccination non-responders. A variety of intra-mu...
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description | Background
Hepatitis B virus (HBV) vaccination is essential in chronic liver disease (CLD), because it can help prevent acute-on-chronic disease, which has potentially fatal complications. Unfortunately, this group has a significant proportion of HBV vaccination non-responders. A variety of intra-muscular (IM) vaccination methods have been used in an attempt to remedy this poor-response, but with limited success.
Aims
Herein is reported the safety and efficacy of high-dose intra-dermal (ID) HBV vaccination in CLD individuals who had failed previous IM standard and boost-dosing regimens.
Methods
Forty-eight CLD individuals, known HBcAb negative, who had failed both a three-dose schedule of 40 μg IM vaccination, and boost dosing of either 40 or 80 μg IM, were identified, of which 42 completed the vaccination course. Each received a 40 μg ID total dose (20 μg per arm) during their clinic visits until a response was documented or a maximum of three doses had been administered. HBsAb titer ≥10 mIU/ml was regarded as an immunologic response; the intention was to achieve an optimum response of ≥100 mIU/ml.
Results
Twenty-nine of forty-two (69%) individuals had an immunologic response, with 15 (51%) of the responders having the optimum response. No changes in serologic data occurred. No serious dermatologic reactions were observed. No differences between those who responded and those who did not were observed with regard to the presence of cirrhosis, diabetes mellitus, or chronic kidney disease.
Conclusions
High-dose ID HBV vaccination of previous CLD non-responders to the standard IM regimen with boost dosing is both safe and efficacious, and should be considered for all such groups. |
doi_str_mv | 10.1007/s10620-011-1996-0 |
format | Article |
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Hepatitis B virus (HBV) vaccination is essential in chronic liver disease (CLD), because it can help prevent acute-on-chronic disease, which has potentially fatal complications. Unfortunately, this group has a significant proportion of HBV vaccination non-responders. A variety of intra-muscular (IM) vaccination methods have been used in an attempt to remedy this poor-response, but with limited success.
Aims
Herein is reported the safety and efficacy of high-dose intra-dermal (ID) HBV vaccination in CLD individuals who had failed previous IM standard and boost-dosing regimens.
Methods
Forty-eight CLD individuals, known HBcAb negative, who had failed both a three-dose schedule of 40 μg IM vaccination, and boost dosing of either 40 or 80 μg IM, were identified, of which 42 completed the vaccination course. Each received a 40 μg ID total dose (20 μg per arm) during their clinic visits until a response was documented or a maximum of three doses had been administered. HBsAb titer ≥10 mIU/ml was regarded as an immunologic response; the intention was to achieve an optimum response of ≥100 mIU/ml.
Results
Twenty-nine of forty-two (69%) individuals had an immunologic response, with 15 (51%) of the responders having the optimum response. No changes in serologic data occurred. No serious dermatologic reactions were observed. No differences between those who responded and those who did not were observed with regard to the presence of cirrhosis, diabetes mellitus, or chronic kidney disease.
Conclusions
High-dose ID HBV vaccination of previous CLD non-responders to the standard IM regimen with boost dosing is both safe and efficacious, and should be considered for all such groups.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-011-1996-0</identifier><identifier>PMID: 22160636</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Adult ; Aged ; Biochemistry ; Chronic Disease ; Chronic illnesses ; Chronic kidney failure ; Complications and side effects ; Diabetes ; Dose-Response Relationship, Drug ; Female ; Gastroenterology ; Hepatitis B ; Hepatitis B - prevention & control ; Hepatitis B Surface Antigens - blood ; Hepatitis B vaccine ; Hepatitis B Vaccines - administration & dosage ; Hepatitis B Vaccines - adverse effects ; Hepatitis B Vaccines - therapeutic use ; Hepatitis B virus ; Hepatitis B virus - immunology ; Hepatology ; Humans ; Immunization ; Injections, Intradermal ; Liver cirrhosis ; Liver diseases ; Liver Diseases - blood ; Liver Diseases - immunology ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Oncology ; Original Article ; Practice Patterns, Physicians ; Retrospective Studies ; Transplant Surgery ; Treatment Outcome ; Vaccination</subject><ispartof>Digestive diseases and sciences, 2012, Vol.57 (1), p.215-220</ispartof><rights>Springer Science+Business Media, LLC 2011</rights><rights>COPYRIGHT 2012 Springer</rights><rights>Springer Science+Business Media, LLC 2011.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-1c21a4dd0d9478520c120c9176cbcadd0cc9ad6834f22a9c86c1695ff4a1afff3</citedby><cites>FETCH-LOGICAL-c497t-1c21a4dd0d9478520c120c9176cbcadd0cc9ad6834f22a9c86c1695ff4a1afff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10620-011-1996-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10620-011-1996-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,41495,42564,51326</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22160636$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dhillon, S.</creatorcontrib><creatorcontrib>Moore, C.</creatorcontrib><creatorcontrib>Li, S. D.</creatorcontrib><creatorcontrib>Aziz, A.</creatorcontrib><creatorcontrib>Kakar, A.</creatorcontrib><creatorcontrib>Dosanjh, A.</creatorcontrib><creatorcontrib>Beesla, A.</creatorcontrib><creatorcontrib>Murphy, L.</creatorcontrib><creatorcontrib>Van Thiel, D. H.</creatorcontrib><title>Efficacy of High-Dose Intra-dermal Hepatitis B Virus Vaccine in Previous Vaccination Non-responders with Chronic Liver Disease</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background
Hepatitis B virus (HBV) vaccination is essential in chronic liver disease (CLD), because it can help prevent acute-on-chronic disease, which has potentially fatal complications. Unfortunately, this group has a significant proportion of HBV vaccination non-responders. A variety of intra-muscular (IM) vaccination methods have been used in an attempt to remedy this poor-response, but with limited success.
Aims
Herein is reported the safety and efficacy of high-dose intra-dermal (ID) HBV vaccination in CLD individuals who had failed previous IM standard and boost-dosing regimens.
Methods
Forty-eight CLD individuals, known HBcAb negative, who had failed both a three-dose schedule of 40 μg IM vaccination, and boost dosing of either 40 or 80 μg IM, were identified, of which 42 completed the vaccination course. Each received a 40 μg ID total dose (20 μg per arm) during their clinic visits until a response was documented or a maximum of three doses had been administered. HBsAb titer ≥10 mIU/ml was regarded as an immunologic response; the intention was to achieve an optimum response of ≥100 mIU/ml.
Results
Twenty-nine of forty-two (69%) individuals had an immunologic response, with 15 (51%) of the responders having the optimum response. No changes in serologic data occurred. No serious dermatologic reactions were observed. No differences between those who responded and those who did not were observed with regard to the presence of cirrhosis, diabetes mellitus, or chronic kidney disease.
Conclusions
High-dose ID HBV vaccination of previous CLD non-responders to the standard IM regimen with boost dosing is both safe and efficacious, and should be considered for all such groups.</description><subject>Adult</subject><subject>Aged</subject><subject>Biochemistry</subject><subject>Chronic Disease</subject><subject>Chronic illnesses</subject><subject>Chronic kidney failure</subject><subject>Complications and side effects</subject><subject>Diabetes</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Hepatitis B</subject><subject>Hepatitis B - prevention & control</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B vaccine</subject><subject>Hepatitis B Vaccines - administration & dosage</subject><subject>Hepatitis B Vaccines - adverse effects</subject><subject>Hepatitis B Vaccines - therapeutic use</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Immunization</subject><subject>Injections, Intradermal</subject><subject>Liver cirrhosis</subject><subject>Liver diseases</subject><subject>Liver Diseases - blood</subject><subject>Liver Diseases - immunology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Practice Patterns, Physicians</subject><subject>Retrospective Studies</subject><subject>Transplant Surgery</subject><subject>Treatment Outcome</subject><subject>Vaccination</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kkFvVCEQx4nR2HX1A3gxRA-eqAz7HizHdlvdJhv1oL0SyoNdmvdghbc1vfjZnc3WNhobQiDD7z8Mw5-Q18CPgXP1oQKXgjMOwEBryfgTMoFWzZho5fwpmXCQuAeQR-RFrdecc61APidHQoDkciYn5Nd5CNFZd0tzoMu43rCzXD29SGOxrPNlsD1d-q0d4xgrPaWXsewqvbTOxeRpTPRr8Tcx38cQzIl-zokVX7c5YYpKf8ZxQxebklN0dBVvfKFnsXpb_UvyLNi--ld365R8_3j-bbFkqy-fLhYnK-YarUYGToBtuo53ulHzVnAHODUo6a6cxbhz2nZyPmuCEFa7uXQgdRtCY8GGEGZT8v6Qd1vyj52voxlidb7vbfJYvNFtIxuusHdT8vYf8jrvSsLijIamFVLrFqF3j0EItAqrE-KBWtvem5hCxqa6_cXmROGvzBTXDVLH_6FwdH6ILicfIsb_EsBB4EqutfhgtiUOttwa4GbvC3PwhUFfmL0vDEfNm7uCd1eD7-4Vf4yAgDgAFY_S2peHFz2e9Tcn68DN</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Dhillon, S.</creator><creator>Moore, C.</creator><creator>Li, S. D.</creator><creator>Aziz, A.</creator><creator>Kakar, A.</creator><creator>Dosanjh, A.</creator><creator>Beesla, A.</creator><creator>Murphy, L.</creator><creator>Van Thiel, D. H.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>2012</creationdate><title>Efficacy of High-Dose Intra-dermal Hepatitis B Virus Vaccine in Previous Vaccination Non-responders with Chronic Liver Disease</title><author>Dhillon, S. ; Moore, C. ; Li, S. D. ; Aziz, A. ; Kakar, A. ; Dosanjh, A. ; Beesla, A. ; Murphy, L. ; Van Thiel, D. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-1c21a4dd0d9478520c120c9176cbcadd0cc9ad6834f22a9c86c1695ff4a1afff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biochemistry</topic><topic>Chronic Disease</topic><topic>Chronic illnesses</topic><topic>Chronic kidney failure</topic><topic>Complications and side effects</topic><topic>Diabetes</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Gastroenterology</topic><topic>Hepatitis B</topic><topic>Hepatitis B - prevention & control</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B vaccine</topic><topic>Hepatitis B Vaccines - administration & dosage</topic><topic>Hepatitis B Vaccines - adverse effects</topic><topic>Hepatitis B Vaccines - therapeutic use</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Immunization</topic><topic>Injections, Intradermal</topic><topic>Liver cirrhosis</topic><topic>Liver diseases</topic><topic>Liver Diseases - blood</topic><topic>Liver Diseases - immunology</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Practice Patterns, Physicians</topic><topic>Retrospective Studies</topic><topic>Transplant Surgery</topic><topic>Treatment Outcome</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dhillon, S.</creatorcontrib><creatorcontrib>Moore, C.</creatorcontrib><creatorcontrib>Li, S. 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H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dhillon, S.</au><au>Moore, C.</au><au>Li, S. D.</au><au>Aziz, A.</au><au>Kakar, A.</au><au>Dosanjh, A.</au><au>Beesla, A.</au><au>Murphy, L.</au><au>Van Thiel, D. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of High-Dose Intra-dermal Hepatitis B Virus Vaccine in Previous Vaccination Non-responders with Chronic Liver Disease</atitle><jtitle>Digestive diseases and sciences</jtitle><stitle>Dig Dis Sci</stitle><addtitle>Dig Dis Sci</addtitle><date>2012</date><risdate>2012</risdate><volume>57</volume><issue>1</issue><spage>215</spage><epage>220</epage><pages>215-220</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><abstract>Background
Hepatitis B virus (HBV) vaccination is essential in chronic liver disease (CLD), because it can help prevent acute-on-chronic disease, which has potentially fatal complications. Unfortunately, this group has a significant proportion of HBV vaccination non-responders. A variety of intra-muscular (IM) vaccination methods have been used in an attempt to remedy this poor-response, but with limited success.
Aims
Herein is reported the safety and efficacy of high-dose intra-dermal (ID) HBV vaccination in CLD individuals who had failed previous IM standard and boost-dosing regimens.
Methods
Forty-eight CLD individuals, known HBcAb negative, who had failed both a three-dose schedule of 40 μg IM vaccination, and boost dosing of either 40 or 80 μg IM, were identified, of which 42 completed the vaccination course. Each received a 40 μg ID total dose (20 μg per arm) during their clinic visits until a response was documented or a maximum of three doses had been administered. HBsAb titer ≥10 mIU/ml was regarded as an immunologic response; the intention was to achieve an optimum response of ≥100 mIU/ml.
Results
Twenty-nine of forty-two (69%) individuals had an immunologic response, with 15 (51%) of the responders having the optimum response. No changes in serologic data occurred. No serious dermatologic reactions were observed. No differences between those who responded and those who did not were observed with regard to the presence of cirrhosis, diabetes mellitus, or chronic kidney disease.
Conclusions
High-dose ID HBV vaccination of previous CLD non-responders to the standard IM regimen with boost dosing is both safe and efficacious, and should be considered for all such groups.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22160636</pmid><doi>10.1007/s10620-011-1996-0</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biochemistry Chronic Disease Chronic illnesses Chronic kidney failure Complications and side effects Diabetes Dose-Response Relationship, Drug Female Gastroenterology Hepatitis B Hepatitis B - prevention & control Hepatitis B Surface Antigens - blood Hepatitis B vaccine Hepatitis B Vaccines - administration & dosage Hepatitis B Vaccines - adverse effects Hepatitis B Vaccines - therapeutic use Hepatitis B virus Hepatitis B virus - immunology Hepatology Humans Immunization Injections, Intradermal Liver cirrhosis Liver diseases Liver Diseases - blood Liver Diseases - immunology Male Medicine Medicine & Public Health Middle Aged Oncology Original Article Practice Patterns, Physicians Retrospective Studies Transplant Surgery Treatment Outcome Vaccination |
title | Efficacy of High-Dose Intra-dermal Hepatitis B Virus Vaccine in Previous Vaccination Non-responders with Chronic Liver Disease |
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