Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus

Extremely early diagnosis of human immunodeficiency virus (HIV) infection has been considered highly important for its treatment. We conducted a performance assessment of a newly developed rapid diagnostic reagent for HIV by using a fourth-generation immunochromatographic assay (Alere HIV Combo). We...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Kansenshogaku Zasshi 2015/11/20, Vol.89(6), pp.733-740
Hauptverfasser: NAKAGIRI, Itsuhiro, WADA, Hideho, TOKUNAGA, Hirotoshi, FUKUDA, Hirofumi, TASAKA, Taizo, SUGIHARA, Takashi
Format: Artikel
Sprache:eng ; jpn
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 740
container_issue 6
container_start_page 733
container_title Kansenshogaku Zasshi
container_volume 89
creator NAKAGIRI, Itsuhiro
WADA, Hideho
TOKUNAGA, Hirotoshi
FUKUDA, Hirofumi
TASAKA, Taizo
SUGIHARA, Takashi
description Extremely early diagnosis of human immunodeficiency virus (HIV) infection has been considered highly important for its treatment. We conducted a performance assessment of a newly developed rapid diagnostic reagent for HIV by using a fourth-generation immunochromatographic assay (Alere HIV Combo). We used whole-blood, plasma, and serum samples obtained from 250 Japanese adults who visited the Kawasaki Medical School Hospital and underwent HIV screening tests. We also used 12 types of commercial HIV-1 seroconversion panels and World Health Organization standard antigens. This method, which has a detection sensitivity of 100% and a specificity of 99.3%, was as accurate as the chemiluminescent immunoassay (CLIA) method. In a sensitivity test using seroconversion panels in the early phase of infection, the mean duration until positive conversion was 19.3 days. With this method having a high detection sensitivity for HIV-1p24 antigen, the results from whole-blood samples were the same as those from plasma and serum samples. Therefore, it can be considered as a useful rapid measurement method for general practice.
doi_str_mv 10.11150/kansenshogakuzasshi.89.733
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1761470351</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1761470351</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3593-ae6178e13d2279a0380f061ffdd67c346345f66b6f64f1d38e442fae8059e1f83</originalsourceid><addsrcrecordid>eNp1kE1vEzEURS0EolHpX0CW2LCZ1B9jj0esqpbSSgWqChA7y_E8J6Yz4-CXKUp_PYaErOjqbc69V-8Q8oazOedcsdN7NyKMuEpLdz89OsRVnJt23kj5jMy4MXWldPv9OZkxaZpKtZwfkRPEuGCMtTUTSrwkR0IbwZUQMwK3kEPKgxs90DNEQBxg3NAUqKOf4Fe_pRfwAH1aQ0fv3Dp29CK65ZhwEz29A7f8Q5cGejWVEno9DNOYOgjRRxj9ln6LecJX5EVwPcLJ_h6Tr5fvv5xfVTefP1yfn91UXqpWVg40bwxw2QnRtK58wALTPISu042XtZa1ClovdNB14J00UNciODBMtcCDkcfk7a53ndPPCXBjh4ge-t6NkCa0vNG8bphUvKDvdqjPCTFDsOscB5e3ljP7V7X9j2prWltUl_Tr_dC0GKA7ZP-JLcDHHfADN8XRAXC5eOvhqW69HzhwfuWyhVH-Boqwn3k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1761470351</pqid></control><display><type>article</type><title>Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>J-STAGE (Japan Science &amp; Technology Information Aggregator, Electronic) Freely Available Titles - Japanese</source><source>Alma/SFX Local Collection</source><creator>NAKAGIRI, Itsuhiro ; WADA, Hideho ; TOKUNAGA, Hirotoshi ; FUKUDA, Hirofumi ; TASAKA, Taizo ; SUGIHARA, Takashi</creator><creatorcontrib>NAKAGIRI, Itsuhiro ; WADA, Hideho ; TOKUNAGA, Hirotoshi ; FUKUDA, Hirofumi ; TASAKA, Taizo ; SUGIHARA, Takashi</creatorcontrib><description>Extremely early diagnosis of human immunodeficiency virus (HIV) infection has been considered highly important for its treatment. We conducted a performance assessment of a newly developed rapid diagnostic reagent for HIV by using a fourth-generation immunochromatographic assay (Alere HIV Combo). We used whole-blood, plasma, and serum samples obtained from 250 Japanese adults who visited the Kawasaki Medical School Hospital and underwent HIV screening tests. We also used 12 types of commercial HIV-1 seroconversion panels and World Health Organization standard antigens. This method, which has a detection sensitivity of 100% and a specificity of 99.3%, was as accurate as the chemiluminescent immunoassay (CLIA) method. In a sensitivity test using seroconversion panels in the early phase of infection, the mean duration until positive conversion was 19.3 days. With this method having a high detection sensitivity for HIV-1p24 antigen, the results from whole-blood samples were the same as those from plasma and serum samples. Therefore, it can be considered as a useful rapid measurement method for general practice.</description><identifier>ISSN: 0387-5911</identifier><identifier>EISSN: 1884-569X</identifier><identifier>DOI: 10.11150/kansenshogakuzasshi.89.733</identifier><identifier>PMID: 26821522</identifier><language>eng ; jpn</language><publisher>Japan: The Japanese Association for Infectious Diseases</publisher><subject>Adult ; Chromatography, Affinity - methods ; HIV Antibodies - immunology ; HIV Antigens - analysis ; HIV Infections - diagnosis ; HIV screening tests ; HIV-1 - immunology ; HIV-1 - isolation &amp; purification ; HIV-1p24 antigen ; Humans ; immunochromatographic assay ; Middle Aged ; whole-blood sample</subject><ispartof>Kansenshogaku Zasshi, 2015/11/20, Vol.89(6), pp.733-740</ispartof><rights>2015 The Japansese Association for Infectious Diseases</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3593-ae6178e13d2279a0380f061ffdd67c346345f66b6f64f1d38e442fae8059e1f83</citedby><cites>FETCH-LOGICAL-c3593-ae6178e13d2279a0380f061ffdd67c346345f66b6f64f1d38e442fae8059e1f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26821522$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NAKAGIRI, Itsuhiro</creatorcontrib><creatorcontrib>WADA, Hideho</creatorcontrib><creatorcontrib>TOKUNAGA, Hirotoshi</creatorcontrib><creatorcontrib>FUKUDA, Hirofumi</creatorcontrib><creatorcontrib>TASAKA, Taizo</creatorcontrib><creatorcontrib>SUGIHARA, Takashi</creatorcontrib><title>Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus</title><title>Kansenshogaku Zasshi</title><addtitle>J. J. A. Inf. D</addtitle><description>Extremely early diagnosis of human immunodeficiency virus (HIV) infection has been considered highly important for its treatment. We conducted a performance assessment of a newly developed rapid diagnostic reagent for HIV by using a fourth-generation immunochromatographic assay (Alere HIV Combo). We used whole-blood, plasma, and serum samples obtained from 250 Japanese adults who visited the Kawasaki Medical School Hospital and underwent HIV screening tests. We also used 12 types of commercial HIV-1 seroconversion panels and World Health Organization standard antigens. This method, which has a detection sensitivity of 100% and a specificity of 99.3%, was as accurate as the chemiluminescent immunoassay (CLIA) method. In a sensitivity test using seroconversion panels in the early phase of infection, the mean duration until positive conversion was 19.3 days. With this method having a high detection sensitivity for HIV-1p24 antigen, the results from whole-blood samples were the same as those from plasma and serum samples. Therefore, it can be considered as a useful rapid measurement method for general practice.</description><subject>Adult</subject><subject>Chromatography, Affinity - methods</subject><subject>HIV Antibodies - immunology</subject><subject>HIV Antigens - analysis</subject><subject>HIV Infections - diagnosis</subject><subject>HIV screening tests</subject><subject>HIV-1 - immunology</subject><subject>HIV-1 - isolation &amp; purification</subject><subject>HIV-1p24 antigen</subject><subject>Humans</subject><subject>immunochromatographic assay</subject><subject>Middle Aged</subject><subject>whole-blood sample</subject><issn>0387-5911</issn><issn>1884-569X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1vEzEURS0EolHpX0CW2LCZ1B9jj0esqpbSSgWqChA7y_E8J6Yz4-CXKUp_PYaErOjqbc69V-8Q8oazOedcsdN7NyKMuEpLdz89OsRVnJt23kj5jMy4MXWldPv9OZkxaZpKtZwfkRPEuGCMtTUTSrwkR0IbwZUQMwK3kEPKgxs90DNEQBxg3NAUqKOf4Fe_pRfwAH1aQ0fv3Dp29CK65ZhwEz29A7f8Q5cGejWVEno9DNOYOgjRRxj9ln6LecJX5EVwPcLJ_h6Tr5fvv5xfVTefP1yfn91UXqpWVg40bwxw2QnRtK58wALTPISu042XtZa1ClovdNB14J00UNciODBMtcCDkcfk7a53ndPPCXBjh4ge-t6NkCa0vNG8bphUvKDvdqjPCTFDsOscB5e3ljP7V7X9j2prWltUl_Tr_dC0GKA7ZP-JLcDHHfADN8XRAXC5eOvhqW69HzhwfuWyhVH-Boqwn3k</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>NAKAGIRI, Itsuhiro</creator><creator>WADA, Hideho</creator><creator>TOKUNAGA, Hirotoshi</creator><creator>FUKUDA, Hirofumi</creator><creator>TASAKA, Taizo</creator><creator>SUGIHARA, Takashi</creator><general>The Japanese Association for Infectious Diseases</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>7X8</scope></search><sort><creationdate>20151101</creationdate><title>Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus</title><author>NAKAGIRI, Itsuhiro ; WADA, Hideho ; TOKUNAGA, Hirotoshi ; FUKUDA, Hirofumi ; TASAKA, Taizo ; SUGIHARA, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3593-ae6178e13d2279a0380f061ffdd67c346345f66b6f64f1d38e442fae8059e1f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Chromatography, Affinity - methods</topic><topic>HIV Antibodies - immunology</topic><topic>HIV Antigens - analysis</topic><topic>HIV Infections - diagnosis</topic><topic>HIV screening tests</topic><topic>HIV-1 - immunology</topic><topic>HIV-1 - isolation &amp; purification</topic><topic>HIV-1p24 antigen</topic><topic>Humans</topic><topic>immunochromatographic assay</topic><topic>Middle Aged</topic><topic>whole-blood sample</topic><toplevel>online_resources</toplevel><creatorcontrib>NAKAGIRI, Itsuhiro</creatorcontrib><creatorcontrib>WADA, Hideho</creatorcontrib><creatorcontrib>TOKUNAGA, Hirotoshi</creatorcontrib><creatorcontrib>FUKUDA, Hirofumi</creatorcontrib><creatorcontrib>TASAKA, Taizo</creatorcontrib><creatorcontrib>SUGIHARA, Takashi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Kansenshogaku Zasshi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NAKAGIRI, Itsuhiro</au><au>WADA, Hideho</au><au>TOKUNAGA, Hirotoshi</au><au>FUKUDA, Hirofumi</au><au>TASAKA, Taizo</au><au>SUGIHARA, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus</atitle><jtitle>Kansenshogaku Zasshi</jtitle><addtitle>J. J. A. Inf. D</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>89</volume><issue>6</issue><spage>733</spage><epage>740</epage><pages>733-740</pages><issn>0387-5911</issn><eissn>1884-569X</eissn><abstract>Extremely early diagnosis of human immunodeficiency virus (HIV) infection has been considered highly important for its treatment. We conducted a performance assessment of a newly developed rapid diagnostic reagent for HIV by using a fourth-generation immunochromatographic assay (Alere HIV Combo). We used whole-blood, plasma, and serum samples obtained from 250 Japanese adults who visited the Kawasaki Medical School Hospital and underwent HIV screening tests. We also used 12 types of commercial HIV-1 seroconversion panels and World Health Organization standard antigens. This method, which has a detection sensitivity of 100% and a specificity of 99.3%, was as accurate as the chemiluminescent immunoassay (CLIA) method. In a sensitivity test using seroconversion panels in the early phase of infection, the mean duration until positive conversion was 19.3 days. With this method having a high detection sensitivity for HIV-1p24 antigen, the results from whole-blood samples were the same as those from plasma and serum samples. Therefore, it can be considered as a useful rapid measurement method for general practice.</abstract><cop>Japan</cop><pub>The Japanese Association for Infectious Diseases</pub><pmid>26821522</pmid><doi>10.11150/kansenshogakuzasshi.89.733</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0387-5911
ispartof Kansenshogaku Zasshi, 2015/11/20, Vol.89(6), pp.733-740
issn 0387-5911
1884-569X
language eng ; jpn
recordid cdi_proquest_miscellaneous_1761470351
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Alma/SFX Local Collection
subjects Adult
Chromatography, Affinity - methods
HIV Antibodies - immunology
HIV Antigens - analysis
HIV Infections - diagnosis
HIV screening tests
HIV-1 - immunology
HIV-1 - isolation & purification
HIV-1p24 antigen
Humans
immunochromatographic assay
Middle Aged
whole-blood sample
title Performance Assessment of a Newly Developed Rapid Diagnostic Reagent for Human Immunodeficiency Virus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A00%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Performance%20Assessment%20of%20a%20Newly%20Developed%20Rapid%20Diagnostic%20Reagent%20for%20Human%20Immunodeficiency%20Virus&rft.jtitle=Kansenshogaku%20Zasshi&rft.au=NAKAGIRI,%20Itsuhiro&rft.date=2015-11-01&rft.volume=89&rft.issue=6&rft.spage=733&rft.epage=740&rft.pages=733-740&rft.issn=0387-5911&rft.eissn=1884-569X&rft_id=info:doi/10.11150/kansenshogakuzasshi.89.733&rft_dat=%3Cproquest_cross%3E1761470351%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1761470351&rft_id=info:pmid/26821522&rfr_iscdi=true