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
Hauptverfasser: Wheeley, Susan M., Jackson, Paul T., Boxall, Elizabeth H, Tarlow, Michael J., Gatrad, A. Rashid, Anderson, Janet, Bissenden, Jeffrey
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container_end_page 215
container_issue 3
container_start_page 212
container_title Journal of medical virology
container_volume 35
creator Wheeley, Susan M.
Jackson, Paul T.
Boxall, Elizabeth H
Tarlow, Michael J.
Gatrad, A. Rashid
Anderson, Janet
Bissenden, Jeffrey
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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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 &amp; 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 &amp; purification</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunization Schedule</subject><subject>Immunoglobulins - administration &amp; 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 &amp; 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 &amp; 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 &amp; purification</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunization Schedule</topic><topic>Immunoglobulins - administration &amp; 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 &amp; 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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