Loading…
Antibody Response of the Newborn After Herpes Simplex Virus Infection
Antibody responses to herpes simplex virus (HSV) types 1and 2, as determined by enzyme-linked immunoabsorbent assay (ELISA), neutralization, and immunoblot, were assessed in sera from newborns with documented HSV infections. The antibody response of the newborns was defined by disease duration and c...
Saved in:
Published in: | The Journal of infectious diseases 1988-11, Vol.158 (5), p.925-933 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c414t-c3a753afb18c71c1761fed6cdde5d34e9de8db56350c95210355c750afd114a43 |
---|---|
cites | |
container_end_page | 933 |
container_issue | 5 |
container_start_page | 925 |
container_title | The Journal of infectious diseases |
container_volume | 158 |
creator | Kahlon, Jasbir Whitley, Richard J. |
description | Antibody responses to herpes simplex virus (HSV) types 1and 2, as determined by enzyme-linked immunoabsorbent assay (ELISA), neutralization, and immunoblot, were assessed in sera from newborns with documented HSV infections. The antibody response of the newborns was defined by disease duration and correlated with disease classification and outcome. Three unique observations were made. First, the quantity of total antibodies at presentation, as determined by ELISA and neutralization, was not predictive of disease classification or outcome. Second, the frequency and intensity of antibody responses to immunologically recognized HSV polypeptides in newborns with central nervous system and disseminated infections were greater than those in newborns with infections localized to the skin, eye, and mouth. Third, the long-term outcome in HSV-infected newborns could be predicted by the quantity of antibodies to the immediate-early infected cell polypeptide ICP 4. These data provide insight into host response to individual polypeptides and their potential value in predicting long-term prognosis. |
doi_str_mv | 10.1093/infdis/158.5.925 |
format | article |
fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_78502648</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>30136590</jstor_id><sourcerecordid>30136590</sourcerecordid><originalsourceid>FETCH-LOGICAL-c414t-c3a753afb18c71c1761fed6cdde5d34e9de8db56350c95210355c750afd114a43</originalsourceid><addsrcrecordid>eNqFkE1v1DAURS0EKkNhzwYpC8QuU784z3aWw6gwlSo-ClQVG8uxn0VKJg52RrT_nlQzDEtWd3HuvYvD2EvgS-CNOOuG4Lt8BqiXuGwqfMQWgEKVUoJ4zBacV1UJummesmc533LOayHVCTupdC0VwIKdr4apa6O_L64oj3HIVMRQTD-o-EC_25iGYhUmSsWG0ki5-NJtx57uiusu7XJxMQRyUxeH5-xJsH2mF4c8Zd_enX9db8rLj-8v1qvL0tVQT6UTVqGwoQXtFDhQEgJ56bwn9KKmxpP2LUqB3DVYAReITiG3wQPUthan7M3-d0zx147yZLZddtT3dqC4y0Zp5JWs9X-LgBVXWj8U-b7oUsw5UTBj6rY23Rvg5kGx2SueF9qgmRXPk1eH7127JX8cHJzO_PWB2-xsH5Id3Hzwt6Z4hSCafze3eYrpiAUHIbHhMy_3vMsT3R25TT-NVEKh2dx8N3i1fnvTXH8yn8UfPTydpg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15207888</pqid></control><display><type>article</type><title>Antibody Response of the Newborn After Herpes Simplex Virus Infection</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Oxford University Press Archive</source><creator>Kahlon, Jasbir ; Whitley, Richard J.</creator><creatorcontrib>Kahlon, Jasbir ; Whitley, Richard J.</creatorcontrib><description>Antibody responses to herpes simplex virus (HSV) types 1and 2, as determined by enzyme-linked immunoabsorbent assay (ELISA), neutralization, and immunoblot, were assessed in sera from newborns with documented HSV infections. The antibody response of the newborns was defined by disease duration and correlated with disease classification and outcome. Three unique observations were made. First, the quantity of total antibodies at presentation, as determined by ELISA and neutralization, was not predictive of disease classification or outcome. Second, the frequency and intensity of antibody responses to immunologically recognized HSV polypeptides in newborns with central nervous system and disseminated infections were greater than those in newborns with infections localized to the skin, eye, and mouth. Third, the long-term outcome in HSV-infected newborns could be predicted by the quantity of antibodies to the immediate-early infected cell polypeptide ICP 4. These data provide insight into host response to individual polypeptides and their potential value in predicting long-term prognosis.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/158.5.925</identifier><identifier>PMID: 2846711</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Antibodies ; Antibodies, Viral - biosynthesis ; Antibody formation ; Biological and medical sciences ; Central nervous system diseases ; Enzyme linked immunosorbent assay ; Health outcomes ; Herpes Simplex - immunology ; Human viral diseases ; Humans ; Immediate-Early Proteins ; Immunoblotting ; Immunoglobulin G - biosynthesis ; Immunoglobulin M - biosynthesis ; Infant, Newborn ; Infections ; Infectious diseases ; Medical sciences ; Neonatal diseases ; Nervous system diseases ; Neutralization Tests ; Newborns ; Original Articles ; Peptides - immunology ; Simplexvirus ; Simplexvirus - immunology ; Viral diseases ; Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye ; Viral Proteins - immunology</subject><ispartof>The Journal of infectious diseases, 1988-11, Vol.158 (5), p.925-933</ispartof><rights>Copyright 1988 The University of Chicago</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-c3a753afb18c71c1761fed6cdde5d34e9de8db56350c95210355c750afd114a43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30136590$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30136590$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7025139$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2846711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kahlon, Jasbir</creatorcontrib><creatorcontrib>Whitley, Richard J.</creatorcontrib><title>Antibody Response of the Newborn After Herpes Simplex Virus Infection</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Antibody responses to herpes simplex virus (HSV) types 1and 2, as determined by enzyme-linked immunoabsorbent assay (ELISA), neutralization, and immunoblot, were assessed in sera from newborns with documented HSV infections. The antibody response of the newborns was defined by disease duration and correlated with disease classification and outcome. Three unique observations were made. First, the quantity of total antibodies at presentation, as determined by ELISA and neutralization, was not predictive of disease classification or outcome. Second, the frequency and intensity of antibody responses to immunologically recognized HSV polypeptides in newborns with central nervous system and disseminated infections were greater than those in newborns with infections localized to the skin, eye, and mouth. Third, the long-term outcome in HSV-infected newborns could be predicted by the quantity of antibodies to the immediate-early infected cell polypeptide ICP 4. These data provide insight into host response to individual polypeptides and their potential value in predicting long-term prognosis.</description><subject>Antibodies</subject><subject>Antibodies, Viral - biosynthesis</subject><subject>Antibody formation</subject><subject>Biological and medical sciences</subject><subject>Central nervous system diseases</subject><subject>Enzyme linked immunosorbent assay</subject><subject>Health outcomes</subject><subject>Herpes Simplex - immunology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immediate-Early Proteins</subject><subject>Immunoblotting</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Infant, Newborn</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Neonatal diseases</subject><subject>Nervous system diseases</subject><subject>Neutralization Tests</subject><subject>Newborns</subject><subject>Original Articles</subject><subject>Peptides - immunology</subject><subject>Simplexvirus</subject><subject>Simplexvirus - immunology</subject><subject>Viral diseases</subject><subject>Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye</subject><subject>Viral Proteins - immunology</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAURS0EKkNhzwYpC8QuU784z3aWw6gwlSo-ClQVG8uxn0VKJg52RrT_nlQzDEtWd3HuvYvD2EvgS-CNOOuG4Lt8BqiXuGwqfMQWgEKVUoJ4zBacV1UJummesmc533LOayHVCTupdC0VwIKdr4apa6O_L64oj3HIVMRQTD-o-EC_25iGYhUmSsWG0ki5-NJtx57uiusu7XJxMQRyUxeH5-xJsH2mF4c8Zd_enX9db8rLj-8v1qvL0tVQT6UTVqGwoQXtFDhQEgJ56bwn9KKmxpP2LUqB3DVYAReITiG3wQPUthan7M3-d0zx147yZLZddtT3dqC4y0Zp5JWs9X-LgBVXWj8U-b7oUsw5UTBj6rY23Rvg5kGx2SueF9qgmRXPk1eH7127JX8cHJzO_PWB2-xsH5Id3Hzwt6Z4hSCafze3eYrpiAUHIbHhMy_3vMsT3R25TT-NVEKh2dx8N3i1fnvTXH8yn8UfPTydpg</recordid><startdate>19881101</startdate><enddate>19881101</enddate><creator>Kahlon, Jasbir</creator><creator>Whitley, Richard J.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</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>19881101</creationdate><title>Antibody Response of the Newborn After Herpes Simplex Virus Infection</title><author>Kahlon, Jasbir ; Whitley, Richard J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-c3a753afb18c71c1761fed6cdde5d34e9de8db56350c95210355c750afd114a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Antibodies</topic><topic>Antibodies, Viral - biosynthesis</topic><topic>Antibody formation</topic><topic>Biological and medical sciences</topic><topic>Central nervous system diseases</topic><topic>Enzyme linked immunosorbent assay</topic><topic>Health outcomes</topic><topic>Herpes Simplex - immunology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immediate-Early Proteins</topic><topic>Immunoblotting</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Infant, Newborn</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Neonatal diseases</topic><topic>Nervous system diseases</topic><topic>Neutralization Tests</topic><topic>Newborns</topic><topic>Original Articles</topic><topic>Peptides - immunology</topic><topic>Simplexvirus</topic><topic>Simplexvirus - immunology</topic><topic>Viral diseases</topic><topic>Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye</topic><topic>Viral Proteins - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kahlon, Jasbir</creatorcontrib><creatorcontrib>Whitley, Richard J.</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>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kahlon, Jasbir</au><au>Whitley, Richard J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibody Response of the Newborn After Herpes Simplex Virus Infection</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>1988-11-01</date><risdate>1988</risdate><volume>158</volume><issue>5</issue><spage>925</spage><epage>933</epage><pages>925-933</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Antibody responses to herpes simplex virus (HSV) types 1and 2, as determined by enzyme-linked immunoabsorbent assay (ELISA), neutralization, and immunoblot, were assessed in sera from newborns with documented HSV infections. The antibody response of the newborns was defined by disease duration and correlated with disease classification and outcome. Three unique observations were made. First, the quantity of total antibodies at presentation, as determined by ELISA and neutralization, was not predictive of disease classification or outcome. Second, the frequency and intensity of antibody responses to immunologically recognized HSV polypeptides in newborns with central nervous system and disseminated infections were greater than those in newborns with infections localized to the skin, eye, and mouth. Third, the long-term outcome in HSV-infected newborns could be predicted by the quantity of antibodies to the immediate-early infected cell polypeptide ICP 4. These data provide insight into host response to individual polypeptides and their potential value in predicting long-term prognosis.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>2846711</pmid><doi>10.1093/infdis/158.5.925</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1899 |
ispartof | The Journal of infectious diseases, 1988-11, Vol.158 (5), p.925-933 |
issn | 0022-1899 1537-6613 |
language | eng |
recordid | cdi_proquest_miscellaneous_78502648 |
source | JSTOR Archival Journals and Primary Sources Collection; Oxford University Press Archive |
subjects | Antibodies Antibodies, Viral - biosynthesis Antibody formation Biological and medical sciences Central nervous system diseases Enzyme linked immunosorbent assay Health outcomes Herpes Simplex - immunology Human viral diseases Humans Immediate-Early Proteins Immunoblotting Immunoglobulin G - biosynthesis Immunoglobulin M - biosynthesis Infant, Newborn Infections Infectious diseases Medical sciences Neonatal diseases Nervous system diseases Neutralization Tests Newborns Original Articles Peptides - immunology Simplexvirus Simplexvirus - immunology Viral diseases Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye Viral Proteins - immunology |
title | Antibody Response of the Newborn After Herpes Simplex Virus Infection |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T12%3A43%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antibody%20Response%20of%20the%20Newborn%20After%20Herpes%20Simplex%20Virus%20Infection&rft.jtitle=The%20Journal%20of%20infectious%20diseases&rft.au=Kahlon,%20Jasbir&rft.date=1988-11-01&rft.volume=158&rft.issue=5&rft.spage=925&rft.epage=933&rft.pages=925-933&rft.issn=0022-1899&rft.eissn=1537-6613&rft.coden=JIDIAQ&rft_id=info:doi/10.1093/infdis/158.5.925&rft_dat=%3Cjstor_proqu%3E30136590%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c414t-c3a753afb18c71c1761fed6cdde5d34e9de8db56350c95210355c750afd114a43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=15207888&rft_id=info:pmid/2846711&rft_jstor_id=30136590&rfr_iscdi=true |