Laboratory diagnosis of acute measles infections in hospitalized children in Zambia
Laboratory diagnosis of measles infection is rarely performed in developing countries and tends to depend on clinical symptoms alone. We evaluated detection of immunoglobulin M (IgM) antibodies for confirmation of acute measles infection in Zambia. In 149 hospitalized children with clinical diagnosi...
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Veröffentlicht in: | Tropical medicine & international health 1997-07, Vol.2 (7), p.612-616 |
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description | Laboratory diagnosis of measles infection is rarely performed in developing countries and tends to depend on clinical symptoms alone. We evaluated detection of immunoglobulin M (IgM) antibodies for confirmation of acute measles infection in Zambia. In 149 hospitalized children with clinical diagnosis of measles, IgM antibodies were detected in 88.6% (132/149). The IgM‐positive rate increased with time after onset of skin rash and all samples were positive after 4 days. In addition to IgM antibody test, virus isolations from throat swabs using B95a cells were also performed. These were positive in only 20.9% (14/67), and both IgM and virus isolation in combination increased the positive rate to 92.5% (62/67). Vaccinated children had higher neutralizing (Nt) antibody responses and, among IgM‐negative patients, all 4 vaccinated children had high Nt antibodies while all 10 unvaccinated children had negative or low Nt results. The IgM antibody test was proved to be a sensitive method for laboratory confirmation of measles virus infection in developing countries. |
doi_str_mv | 10.1046/j.1365-3156.1997.d01-346.x |
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Vaccinated children had higher neutralizing (Nt) antibody responses and, among IgM‐negative patients, all 4 vaccinated children had high Nt antibodies while all 10 unvaccinated children had negative or low Nt results. The IgM antibody test was proved to be a sensitive method for laboratory confirmation of measles virus infection in developing countries.</description><identifier>ISSN: 1360-2276</identifier><identifier>EISSN: 1365-3156</identifier><identifier>DOI: 10.1046/j.1365-3156.1997.d01-346.x</identifier><identifier>PMID: 9270728</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Acute Disease ; Adolescent ; Antibodies, Viral - blood ; Biological and medical sciences ; Child ; Child, Preschool ; Cross Infection - diagnosis ; Cross Infection - prevention & control ; Cross Infection - virology ; Female ; Human viral diseases ; Humans ; IgM ; Immunoglobulin M - blood ; Infant ; Infectious diseases ; isolation ; Male ; Measles ; Measles - diagnosis ; Measles - prevention & control ; Measles - virology ; Measles Vaccine - immunology ; Measles virus - immunology ; Measles virus - isolation & purification ; Medical sciences ; Pharynx - virology ; Tropical medicine ; vaccine failure ; Viral diseases ; Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye ; Zambia</subject><ispartof>Tropical medicine & international health, 1997-07, Vol.2 (7), p.612-616</ispartof><rights>1997 Blackwell Science Ltd</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4930-704f76b44c2d1e1fe34b7ec12ac5c31e6a230b29c02bfb5aeee49e2826d949c23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-3156.1997.d01-346.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45551,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2742505$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9270728$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oshitani, H.</creatorcontrib><creatorcontrib>Suzuki, H.</creatorcontrib><creatorcontrib>Mpabalwani, M.</creatorcontrib><creatorcontrib>Mizuta, K.</creatorcontrib><creatorcontrib>Kasolo, F. C.</creatorcontrib><creatorcontrib>Luo, N. P.</creatorcontrib><creatorcontrib>Numazaki, Y.</creatorcontrib><title>Laboratory diagnosis of acute measles infections in hospitalized children in Zambia</title><title>Tropical medicine & international health</title><addtitle>Trop Med Int Health</addtitle><description>Laboratory diagnosis of measles infection is rarely performed in developing countries and tends to depend on clinical symptoms alone. We evaluated detection of immunoglobulin M (IgM) antibodies for confirmation of acute measles infection in Zambia. In 149 hospitalized children with clinical diagnosis of measles, IgM antibodies were detected in 88.6% (132/149). The IgM‐positive rate increased with time after onset of skin rash and all samples were positive after 4 days. In addition to IgM antibody test, virus isolations from throat swabs using B95a cells were also performed. These were positive in only 20.9% (14/67), and both IgM and virus isolation in combination increased the positive rate to 92.5% (62/67). Vaccinated children had higher neutralizing (Nt) antibody responses and, among IgM‐negative patients, all 4 vaccinated children had high Nt antibodies while all 10 unvaccinated children had negative or low Nt results. The IgM antibody test was proved to be a sensitive method for laboratory confirmation of measles virus infection in developing countries.</description><subject>Acute Disease</subject><subject>Adolescent</subject><subject>Antibodies, Viral - blood</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cross Infection - diagnosis</subject><subject>Cross Infection - prevention & control</subject><subject>Cross Infection - virology</subject><subject>Female</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>IgM</subject><subject>Immunoglobulin M - blood</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>isolation</subject><subject>Male</subject><subject>Measles</subject><subject>Measles - diagnosis</subject><subject>Measles - prevention & control</subject><subject>Measles - virology</subject><subject>Measles Vaccine - immunology</subject><subject>Measles virus - immunology</subject><subject>Measles virus - isolation & purification</subject><subject>Medical sciences</subject><subject>Pharynx - virology</subject><subject>Tropical medicine</subject><subject>vaccine failure</subject><subject>Viral diseases</subject><subject>Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye</subject><subject>Zambia</subject><issn>1360-2276</issn><issn>1365-3156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEtr20AURofSkCZpf0JBlNKdlHlpxtNFIZg8DA5ZJN10M1yNruoxksadkWmcXx8pNt5ndS985z44hHxjtGBUqst1wYQqc8FKVTBjdFFTlgupiucP5OwYfXzrac65Vp_IeUprSqmUpTolp4ZrqvnsjDwuoQoRhhB3We3hbx-ST1loMnDbAbMOIbWYMt836AYf-qnNViFt_ACtf8E6cyvf1hH7KfgDXeXhMzlpoE345VAvyO-b66f5Xb58uF3Mr5a5k0bQXFPZaFVJ6XjNkDUoZKXRMQ6udIKhAi5oxY2jvGqqEhBRGuQzrmojjePigvzY793E8G-LabCdTw7bFnoM22S14UJLI0fw5x50MaQUsbGb6DuIO8uonYzatZ202UmbnYza0agdjdrncfjr4cq26rA-jh4Ujvn3Qw7JQdtE6J1PR4xryUtajtivPfbft7h7xwP26X5BNRWvKb-TiQ</recordid><startdate>199707</startdate><enddate>199707</enddate><creator>Oshitani, H.</creator><creator>Suzuki, H.</creator><creator>Mpabalwani, M.</creator><creator>Mizuta, K.</creator><creator>Kasolo, F. 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P. ; Numazaki, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4930-704f76b44c2d1e1fe34b7ec12ac5c31e6a230b29c02bfb5aeee49e2826d949c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Acute Disease</topic><topic>Adolescent</topic><topic>Antibodies, Viral - blood</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cross Infection - diagnosis</topic><topic>Cross Infection - prevention & control</topic><topic>Cross Infection - virology</topic><topic>Female</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>IgM</topic><topic>Immunoglobulin M - blood</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>isolation</topic><topic>Male</topic><topic>Measles</topic><topic>Measles - diagnosis</topic><topic>Measles - prevention & control</topic><topic>Measles - virology</topic><topic>Measles Vaccine - immunology</topic><topic>Measles virus - immunology</topic><topic>Measles virus - isolation & purification</topic><topic>Medical sciences</topic><topic>Pharynx - virology</topic><topic>Tropical medicine</topic><topic>vaccine failure</topic><topic>Viral diseases</topic><topic>Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye</topic><topic>Zambia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oshitani, H.</creatorcontrib><creatorcontrib>Suzuki, H.</creatorcontrib><creatorcontrib>Mpabalwani, M.</creatorcontrib><creatorcontrib>Mizuta, K.</creatorcontrib><creatorcontrib>Kasolo, F. 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P.</au><au>Numazaki, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Laboratory diagnosis of acute measles infections in hospitalized children in Zambia</atitle><jtitle>Tropical medicine & international health</jtitle><addtitle>Trop Med Int Health</addtitle><date>1997-07</date><risdate>1997</risdate><volume>2</volume><issue>7</issue><spage>612</spage><epage>616</epage><pages>612-616</pages><issn>1360-2276</issn><eissn>1365-3156</eissn><abstract>Laboratory diagnosis of measles infection is rarely performed in developing countries and tends to depend on clinical symptoms alone. We evaluated detection of immunoglobulin M (IgM) antibodies for confirmation of acute measles infection in Zambia. In 149 hospitalized children with clinical diagnosis of measles, IgM antibodies were detected in 88.6% (132/149). The IgM‐positive rate increased with time after onset of skin rash and all samples were positive after 4 days. In addition to IgM antibody test, virus isolations from throat swabs using B95a cells were also performed. These were positive in only 20.9% (14/67), and both IgM and virus isolation in combination increased the positive rate to 92.5% (62/67). Vaccinated children had higher neutralizing (Nt) antibody responses and, among IgM‐negative patients, all 4 vaccinated children had high Nt antibodies while all 10 unvaccinated children had negative or low Nt results. The IgM antibody test was proved to be a sensitive method for laboratory confirmation of measles virus infection in developing countries.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9270728</pmid><doi>10.1046/j.1365-3156.1997.d01-346.x</doi><tpages>5</tpages></addata></record> |
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subjects | Acute Disease Adolescent Antibodies, Viral - blood Biological and medical sciences Child Child, Preschool Cross Infection - diagnosis Cross Infection - prevention & control Cross Infection - virology Female Human viral diseases Humans IgM Immunoglobulin M - blood Infant Infectious diseases isolation Male Measles Measles - diagnosis Measles - prevention & control Measles - virology Measles Vaccine - immunology Measles virus - immunology Measles virus - isolation & purification Medical sciences Pharynx - virology Tropical medicine vaccine failure Viral diseases Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye Zambia |
title | Laboratory diagnosis of acute measles infections in hospitalized children in Zambia |
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