The challenge of discriminating between HIV‐1, HIV‐2 and HIV‐1/2 dual infections

Objectives Discrimination between HIV‐1 and HIV‐2 is important to ensure appropriate antiretroviral treatment (ART) and epidemiological surveillance. However, serological tests have shown frequent mistyping when applied in the field. We evaluated two confirmatory tests, INNO‐LIA HIV I/II Score and I...

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Veröffentlicht in:HIV medicine 2018-07, Vol.19 (6), p.403-410
Hauptverfasser: Hønge, BL, Jespersen, S, Medina, C, Té, DS, Silva, ZJ, Christiansen, M, Kjerulff, B, Laursen, AL, Wejse, C, Krarup, H, Erikstrup, C, Rodrigues, Amabelia, Silva, David, Oliviera‐Souto, Ines, Østergaard, Lars, Aaby, Peter, Fomsgaard, Anders
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container_end_page 410
container_issue 6
container_start_page 403
container_title HIV medicine
container_volume 19
creator Hønge, BL
Jespersen, S
Medina, C
Té, DS
Silva, ZJ
Christiansen, M
Kjerulff, B
Laursen, AL
Wejse, C
Krarup, H
Erikstrup, C
Rodrigues, Amabelia
Silva, David
Oliviera‐Souto, Ines
Østergaard, Lars
Aaby, Peter
Fomsgaard, Anders
description Objectives Discrimination between HIV‐1 and HIV‐2 is important to ensure appropriate antiretroviral treatment (ART) and epidemiological surveillance. However, serological tests have shown frequent mistyping when applied in the field. We evaluated two confirmatory tests, INNO‐LIA HIV I/II Score and ImmunoComb HIV 1/2 BiSpot, for HIV type discriminatory capacity. Methods Samples from 239 ART‐naïve HIV‐infected patients from the Bissau HIV Cohort in Guinea‐Bissau were selected retrospectively based on the initial HIV typing performed in Bissau, ensuring a broad representation of HIV types. INNO‐LIA results were interpreted by the newest software algorithm, and three independent observers read the ImmunoComb results. HIV‐1/HIV‐2 RNA and DNA were measured for confirmation. Results INNO‐LIA results showed 123 HIV‐1 positive samples, 69 HIV‐2 positive and 47 HIV‐1/2 dually reactive. There was agreement between INNO‐LIA and HIV‐1/HIV‐2 RNA and DNA detection, although not all HIV‐1/2 dually reactive samples could be confirmed by the nucleic acid results. Overall, the observers found that the ImmunoComb results differed from the INNO‐LIA results, with agreements of 90.4, 91.2 and 92.5%, respectively, for HIV‐1, HIV‐2 and HIV‐1/2. The combined kappa‐score for agreement between the three observers was 0.955 (z‐score 35.1; P < 0.01). Of the HIV‐2 mono‐reactive samples (INNO‐LIA), the three observers interpreted 24.6–31.9% as HIV‐1/2 dually infected by ImmunoComb. None of these samples had detectable HIV‐1 RNA or DNA. Conclusions There was accordance between INNO‐LIA calls and nucleic acid results, whereas ImmunoComb overestimated the number of HIV‐1/2 dually infected patients. Confirmatory typing is needed for patients diagnosed with HIV‐1/2 dual infection by ImmunoComb.
doi_str_mv 10.1111/hiv.12606
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However, serological tests have shown frequent mistyping when applied in the field. We evaluated two confirmatory tests, INNO‐LIA HIV I/II Score and ImmunoComb HIV 1/2 BiSpot, for HIV type discriminatory capacity. Methods Samples from 239 ART‐naïve HIV‐infected patients from the Bissau HIV Cohort in Guinea‐Bissau were selected retrospectively based on the initial HIV typing performed in Bissau, ensuring a broad representation of HIV types. INNO‐LIA results were interpreted by the newest software algorithm, and three independent observers read the ImmunoComb results. HIV‐1/HIV‐2 RNA and DNA were measured for confirmation. Results INNO‐LIA results showed 123 HIV‐1 positive samples, 69 HIV‐2 positive and 47 HIV‐1/2 dually reactive. There was agreement between INNO‐LIA and HIV‐1/HIV‐2 RNA and DNA detection, although not all HIV‐1/2 dually reactive samples could be confirmed by the nucleic acid results. Overall, the observers found that the ImmunoComb results differed from the INNO‐LIA results, with agreements of 90.4, 91.2 and 92.5%, respectively, for HIV‐1, HIV‐2 and HIV‐1/2. The combined kappa‐score for agreement between the three observers was 0.955 (z‐score 35.1; P &lt; 0.01). Of the HIV‐2 mono‐reactive samples (INNO‐LIA), the three observers interpreted 24.6–31.9% as HIV‐1/2 dually infected by ImmunoComb. None of these samples had detectable HIV‐1 RNA or DNA. Conclusions There was accordance between INNO‐LIA calls and nucleic acid results, whereas ImmunoComb overestimated the number of HIV‐1/2 dually infected patients. Confirmatory typing is needed for patients diagnosed with HIV‐1/2 dual infection by ImmunoComb.</description><identifier>ISSN: 1464-2662</identifier><identifier>EISSN: 1468-1293</identifier><identifier>DOI: 10.1111/hiv.12606</identifier><identifier>PMID: 29573304</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Antiretroviral agents ; Deoxyribonucleic acid ; DNA ; Epidemiology ; Guinea‐Bissau ; HIV ; HIV type discrimination ; HIV‐2 ; Human immunodeficiency virus ; ImmunoComb ; Infections ; INNO‐LIA ; Observers ; Patients ; Ribonucleic acid ; RNA ; Sampling methods ; Serological tests ; Typing</subject><ispartof>HIV medicine, 2018-07, Vol.19 (6), p.403-410</ispartof><rights>2018 British HIV Association</rights><rights>2018 British HIV Association.</rights><rights>HIV Medicine © 2018 British HIV Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3886-8b4ad08af30f2110ff74ec96a513f227e89d8b7f61e906578d7e6c7ec307d7183</citedby><cites>FETCH-LOGICAL-c3886-8b4ad08af30f2110ff74ec96a513f227e89d8b7f61e906578d7e6c7ec307d7183</cites><orcidid>0000-0002-2534-2942 ; 0000-0001-9636-4519</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhiv.12606$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhiv.12606$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29573304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hønge, BL</creatorcontrib><creatorcontrib>Jespersen, S</creatorcontrib><creatorcontrib>Medina, C</creatorcontrib><creatorcontrib>Té, DS</creatorcontrib><creatorcontrib>Silva, ZJ</creatorcontrib><creatorcontrib>Christiansen, M</creatorcontrib><creatorcontrib>Kjerulff, B</creatorcontrib><creatorcontrib>Laursen, AL</creatorcontrib><creatorcontrib>Wejse, C</creatorcontrib><creatorcontrib>Krarup, H</creatorcontrib><creatorcontrib>Erikstrup, C</creatorcontrib><creatorcontrib>Rodrigues, Amabelia</creatorcontrib><creatorcontrib>Silva, David</creatorcontrib><creatorcontrib>Oliviera‐Souto, Ines</creatorcontrib><creatorcontrib>Østergaard, Lars</creatorcontrib><creatorcontrib>Aaby, Peter</creatorcontrib><creatorcontrib>Fomsgaard, Anders</creatorcontrib><creatorcontrib>Bissau HIV Cohort study group</creatorcontrib><creatorcontrib>the Bissau HIV Cohort study group</creatorcontrib><title>The challenge of discriminating between HIV‐1, HIV‐2 and HIV‐1/2 dual infections</title><title>HIV medicine</title><addtitle>HIV Med</addtitle><description>Objectives Discrimination between HIV‐1 and HIV‐2 is important to ensure appropriate antiretroviral treatment (ART) and epidemiological surveillance. However, serological tests have shown frequent mistyping when applied in the field. We evaluated two confirmatory tests, INNO‐LIA HIV I/II Score and ImmunoComb HIV 1/2 BiSpot, for HIV type discriminatory capacity. Methods Samples from 239 ART‐naïve HIV‐infected patients from the Bissau HIV Cohort in Guinea‐Bissau were selected retrospectively based on the initial HIV typing performed in Bissau, ensuring a broad representation of HIV types. INNO‐LIA results were interpreted by the newest software algorithm, and three independent observers read the ImmunoComb results. HIV‐1/HIV‐2 RNA and DNA were measured for confirmation. Results INNO‐LIA results showed 123 HIV‐1 positive samples, 69 HIV‐2 positive and 47 HIV‐1/2 dually reactive. There was agreement between INNO‐LIA and HIV‐1/HIV‐2 RNA and DNA detection, although not all HIV‐1/2 dually reactive samples could be confirmed by the nucleic acid results. Overall, the observers found that the ImmunoComb results differed from the INNO‐LIA results, with agreements of 90.4, 91.2 and 92.5%, respectively, for HIV‐1, HIV‐2 and HIV‐1/2. The combined kappa‐score for agreement between the three observers was 0.955 (z‐score 35.1; P &lt; 0.01). Of the HIV‐2 mono‐reactive samples (INNO‐LIA), the three observers interpreted 24.6–31.9% as HIV‐1/2 dually infected by ImmunoComb. None of these samples had detectable HIV‐1 RNA or DNA. Conclusions There was accordance between INNO‐LIA calls and nucleic acid results, whereas ImmunoComb overestimated the number of HIV‐1/2 dually infected patients. 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However, serological tests have shown frequent mistyping when applied in the field. We evaluated two confirmatory tests, INNO‐LIA HIV I/II Score and ImmunoComb HIV 1/2 BiSpot, for HIV type discriminatory capacity. Methods Samples from 239 ART‐naïve HIV‐infected patients from the Bissau HIV Cohort in Guinea‐Bissau were selected retrospectively based on the initial HIV typing performed in Bissau, ensuring a broad representation of HIV types. INNO‐LIA results were interpreted by the newest software algorithm, and three independent observers read the ImmunoComb results. HIV‐1/HIV‐2 RNA and DNA were measured for confirmation. Results INNO‐LIA results showed 123 HIV‐1 positive samples, 69 HIV‐2 positive and 47 HIV‐1/2 dually reactive. There was agreement between INNO‐LIA and HIV‐1/HIV‐2 RNA and DNA detection, although not all HIV‐1/2 dually reactive samples could be confirmed by the nucleic acid results. Overall, the observers found that the ImmunoComb results differed from the INNO‐LIA results, with agreements of 90.4, 91.2 and 92.5%, respectively, for HIV‐1, HIV‐2 and HIV‐1/2. The combined kappa‐score for agreement between the three observers was 0.955 (z‐score 35.1; P &lt; 0.01). Of the HIV‐2 mono‐reactive samples (INNO‐LIA), the three observers interpreted 24.6–31.9% as HIV‐1/2 dually infected by ImmunoComb. None of these samples had detectable HIV‐1 RNA or DNA. Conclusions There was accordance between INNO‐LIA calls and nucleic acid results, whereas ImmunoComb overestimated the number of HIV‐1/2 dually infected patients. Confirmatory typing is needed for patients diagnosed with HIV‐1/2 dual infection by ImmunoComb.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29573304</pmid><doi>10.1111/hiv.12606</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2534-2942</orcidid><orcidid>https://orcid.org/0000-0001-9636-4519</orcidid><oa>free_for_read</oa></addata></record>
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; Wiley Free Content
subjects Antiretroviral agents
Deoxyribonucleic acid
DNA
Epidemiology
Guinea‐Bissau
HIV
HIV type discrimination
HIV‐2
Human immunodeficiency virus
ImmunoComb
Infections
INNO‐LIA
Observers
Patients
Ribonucleic acid
RNA
Sampling methods
Serological tests
Typing
title The challenge of discriminating between HIV‐1, HIV‐2 and HIV‐1/2 dual infections
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