Prevention of perinatal transmission of hepatitis B Virus (HB V): A comparison of two prophylactic schedules
Perinatal transmission of hepatitis B virus (HBV) from HBsAg carrier mothers who were HBeAg+, antiHBe+, or negative for both HBe markers, was interrupted using either 4 doses of vaccine, or one dose of hepatitis B immunoglobulin (HBIG) at birth, combined with 4 doses of vaccine. In those infants who...
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Veröffentlicht in: | Journal of medical virology 1991-11, Vol.35 (3), p.212-215 |
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description | Perinatal transmission of hepatitis B virus (HBV) from HBsAg carrier mothers who were HBeAg+, antiHBe+, or negative for both HBe markers, was interrupted using either 4 doses of vaccine, or one dose of hepatitis B immunoglobulin (HBIG) at birth, combined with 4 doses of vaccine. In those infants who received HBlG at birth, the antiHBs titre was significantly higher at 1 and 2 months old, but at 6, 9, and 18 months old, there was no significant difference.
Among the infants of carrier mothers who did not display HBeAg (i.e., were antiHBe+, or negative for both HBe markers), a transient subclinical infection would have been expected in around 10% had there been no intervention. No evidence of such infection was detected, and no difference in outcome was found between the two treatment groups.
Amongst infants born to HBeAg+ carrier mothers, infection occurred in 1 out of 8 who had received HBlG and vaccine, and in 3 of 8 who had received vaccine only. The difference in outcome was not statistically significant, but the numbers analysed were small. The infections which occurred in spite of prophylaxis may be attributable to in utero infection, poor response to vaccine by the infant, or to the mother having a particularly high HBV‐DNA level. HBlG given at birth to infants of HBeAg+ carrier mothers may enhance the protection of infants who are destined to be poor responders to vaccine. |
doi_str_mv | 10.1002/jmv.1890350312 |
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Among the infants of carrier mothers who did not display HBeAg (i.e., were antiHBe+, or negative for both HBe markers), a transient subclinical infection would have been expected in around 10% had there been no intervention. No evidence of such infection was detected, and no difference in outcome was found between the two treatment groups.
Amongst infants born to HBeAg+ carrier mothers, infection occurred in 1 out of 8 who had received HBlG and vaccine, and in 3 of 8 who had received vaccine only. The difference in outcome was not statistically significant, but the numbers analysed were small. The infections which occurred in spite of prophylaxis may be attributable to in utero infection, poor response to vaccine by the infant, or to the mother having a particularly high HBV‐DNA level. HBlG given at birth to infants of HBeAg+ carrier mothers may enhance the protection of infants who are destined to be poor responders to vaccine.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.1890350312</identifier><identifier>PMID: 1839553</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Carrier State ; DNA, Viral - blood ; Female ; Hepatitis B - immunology ; Hepatitis B - prevention & control ; Hepatitis B - transmission ; Hepatitis B Antibodies - blood ; Hepatitis B e Antigens - blood ; hepatitis B im-munoglobulin (HBIG) ; Hepatitis B Vaccines ; hepatitis B virus ; hepatitis B virus (HBV) ; Hepatitis B virus - immunology ; Hepatitis B virus - isolation & purification ; Human viral diseases ; Humans ; Immunization Schedule ; Immunoglobulins - administration & dosage ; Infant, Newborn ; Infectious diseases ; Medical sciences ; perinatal transmission ; Pregnancy ; vaccine ; Viral diseases ; Viral hepatitis ; Viral Hepatitis Vaccines - administration & dosage</subject><ispartof>Journal of medical virology, 1991-11, Vol.35 (3), p.212-215</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-c3532-c650a7e57d47ea0aee794622ce0f2f674e7626929fb0dbf92f2f6d39523098503</citedby><cites>FETCH-LOGICAL-c3532-c650a7e57d47ea0aee794622ce0f2f674e7626929fb0dbf92f2f6d39523098503</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.1890350312$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.1890350312$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5146031$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1839553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wheeley, Susan M.</creatorcontrib><creatorcontrib>Jackson, Paul T.</creatorcontrib><creatorcontrib>Boxall, Elizabeth H</creatorcontrib><creatorcontrib>Tarlow, Michael J.</creatorcontrib><creatorcontrib>Gatrad, A. Rashid</creatorcontrib><creatorcontrib>Anderson, Janet</creatorcontrib><creatorcontrib>Bissenden, Jeffrey</creatorcontrib><title>Prevention of perinatal transmission of hepatitis B Virus (HB V): A comparison of two prophylactic schedules</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Perinatal transmission of hepatitis B virus (HBV) from HBsAg carrier mothers who were HBeAg+, antiHBe+, or negative for both HBe markers, was interrupted using either 4 doses of vaccine, or one dose of hepatitis B immunoglobulin (HBIG) at birth, combined with 4 doses of vaccine. In those infants who received HBlG at birth, the antiHBs titre was significantly higher at 1 and 2 months old, but at 6, 9, and 18 months old, there was no significant difference.
Among the infants of carrier mothers who did not display HBeAg (i.e., were antiHBe+, or negative for both HBe markers), a transient subclinical infection would have been expected in around 10% had there been no intervention. No evidence of such infection was detected, and no difference in outcome was found between the two treatment groups.
Amongst infants born to HBeAg+ carrier mothers, infection occurred in 1 out of 8 who had received HBlG and vaccine, and in 3 of 8 who had received vaccine only. The difference in outcome was not statistically significant, but the numbers analysed were small. The infections which occurred in spite of prophylaxis may be attributable to in utero infection, poor response to vaccine by the infant, or to the mother having a particularly high HBV‐DNA level. HBlG given at birth to infants of HBeAg+ carrier mothers may enhance the protection of infants who are destined to be poor responders to vaccine.</description><subject>Biological and medical sciences</subject><subject>Carrier State</subject><subject>DNA, Viral - blood</subject><subject>Female</subject><subject>Hepatitis B - immunology</subject><subject>Hepatitis B - prevention & control</subject><subject>Hepatitis B - transmission</subject><subject>Hepatitis B Antibodies - blood</subject><subject>Hepatitis B e Antigens - blood</subject><subject>hepatitis B im-munoglobulin (HBIG)</subject><subject>Hepatitis B Vaccines</subject><subject>hepatitis B virus</subject><subject>hepatitis B virus (HBV)</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis B virus - isolation & purification</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunization Schedule</subject><subject>Immunoglobulins - administration & dosage</subject><subject>Infant, Newborn</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>perinatal transmission</subject><subject>Pregnancy</subject><subject>vaccine</subject><subject>Viral diseases</subject><subject>Viral hepatitis</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>eNqFkc1v1DAQxS0EKkvLlRuSDwjBIduxk9gxt1KgLRSoEBSJi-V1Jlq3zgd20rL_fV1l1YpTT7b8fjOeeY-QFwyWDIDvX7RXS1YpyEvIGX9EFgyUyBRI9pgsgBUiE4KVT8mzGC8AoFKc75AdVuWqLPMF8WcBr7AbXd_RvqEDBteZ0Xg6BtPF1sW4VdY4mNGNLtL39NyFKdI3x-n29h09oLZvBxNcnMnxuqdD6If1xhs7OkujXWM9eYx75EljfMTn23OX_Pr08efhcXb6_ejk8OA0s3mZ88yKEozEUtaFRAMGUapCcG4RGt4IWaAUXCiumhXUq0bx29c6LcRzUFXyYZe8nvumMf5OGEedFrHovemwn6KWXEKyhj0IMlEUBS9kApczaEMfY8BGD8G1Jmw0A32bg0456PscUsHLbedp1WJ9j8_GJ_3VVjfRGt8kt62Ld1iZgkt9EqZm7Np53Dzwqf789fy_EbK51sUR_93VmnCphcxlqX9_O9Jw9uVHwf9U-kN-A3tPr4w</recordid><startdate>199111</startdate><enddate>199111</enddate><creator>Wheeley, Susan M.</creator><creator>Jackson, Paul T.</creator><creator>Boxall, Elizabeth H</creator><creator>Tarlow, Michael J.</creator><creator>Gatrad, A. Rashid</creator><creator>Anderson, Janet</creator><creator>Bissenden, Jeffrey</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>Prevention of perinatal transmission of hepatitis B Virus (HB V): A comparison of two prophylactic schedules</title><author>Wheeley, Susan M. ; Jackson, Paul T. ; Boxall, Elizabeth H ; Tarlow, Michael J. ; Gatrad, A. Rashid ; Anderson, Janet ; Bissenden, Jeffrey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3532-c650a7e57d47ea0aee794622ce0f2f674e7626929fb0dbf92f2f6d39523098503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Biological and medical sciences</topic><topic>Carrier State</topic><topic>DNA, Viral - blood</topic><topic>Female</topic><topic>Hepatitis B - immunology</topic><topic>Hepatitis B - prevention & control</topic><topic>Hepatitis B - transmission</topic><topic>Hepatitis B Antibodies - blood</topic><topic>Hepatitis B e Antigens - blood</topic><topic>hepatitis B im-munoglobulin (HBIG)</topic><topic>Hepatitis B Vaccines</topic><topic>hepatitis B virus</topic><topic>hepatitis B virus (HBV)</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatitis B virus - isolation & purification</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunization Schedule</topic><topic>Immunoglobulins - administration & dosage</topic><topic>Infant, Newborn</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>perinatal transmission</topic><topic>Pregnancy</topic><topic>vaccine</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>Viral Hepatitis Vaccines - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wheeley, Susan M.</creatorcontrib><creatorcontrib>Jackson, Paul T.</creatorcontrib><creatorcontrib>Boxall, Elizabeth H</creatorcontrib><creatorcontrib>Tarlow, Michael J.</creatorcontrib><creatorcontrib>Gatrad, A. Rashid</creatorcontrib><creatorcontrib>Anderson, Janet</creatorcontrib><creatorcontrib>Bissenden, Jeffrey</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>Wheeley, Susan M.</au><au>Jackson, Paul T.</au><au>Boxall, Elizabeth H</au><au>Tarlow, Michael J.</au><au>Gatrad, A. Rashid</au><au>Anderson, Janet</au><au>Bissenden, Jeffrey</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of perinatal transmission of hepatitis B Virus (HB V): A comparison of two prophylactic schedules</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>212</spage><epage>215</epage><pages>212-215</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Perinatal transmission of hepatitis B virus (HBV) from HBsAg carrier mothers who were HBeAg+, antiHBe+, or negative for both HBe markers, was interrupted using either 4 doses of vaccine, or one dose of hepatitis B immunoglobulin (HBIG) at birth, combined with 4 doses of vaccine. In those infants who received HBlG at birth, the antiHBs titre was significantly higher at 1 and 2 months old, but at 6, 9, and 18 months old, there was no significant difference.
Among the infants of carrier mothers who did not display HBeAg (i.e., were antiHBe+, or negative for both HBe markers), a transient subclinical infection would have been expected in around 10% had there been no intervention. No evidence of such infection was detected, and no difference in outcome was found between the two treatment groups.
Amongst infants born to HBeAg+ carrier mothers, infection occurred in 1 out of 8 who had received HBlG and vaccine, and in 3 of 8 who had received vaccine only. The difference in outcome was not statistically significant, but the numbers analysed were small. The infections which occurred in spite of prophylaxis may be attributable to in utero infection, poor response to vaccine by the infant, or to the mother having a particularly high HBV‐DNA level. HBlG given at birth to infants of HBeAg+ carrier mothers may enhance the protection of infants who are destined to be poor responders to vaccine.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1839553</pmid><doi>10.1002/jmv.1890350312</doi><tpages>4</tpages></addata></record> |
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subjects | Biological and medical sciences Carrier State DNA, Viral - blood Female Hepatitis B - immunology Hepatitis B - prevention & control Hepatitis B - transmission Hepatitis B Antibodies - blood Hepatitis B e Antigens - blood hepatitis B im-munoglobulin (HBIG) Hepatitis B Vaccines hepatitis B virus hepatitis B virus (HBV) Hepatitis B virus - immunology Hepatitis B virus - isolation & purification Human viral diseases Humans Immunization Schedule Immunoglobulins - administration & dosage Infant, Newborn Infectious diseases Medical sciences perinatal transmission Pregnancy vaccine Viral diseases Viral hepatitis Viral Hepatitis Vaccines - administration & dosage |
title | Prevention of perinatal transmission of hepatitis B Virus (HB V): A comparison of two prophylactic schedules |
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