IFN-[gamma] response on T-cell based assays in HIV-infected patients for detection of tuberculosis infection
Individuals infected with human immunodeficiency virus (HIV) have an increased risk of progression to active tuberculosis following Mycobacterium tuberculosis infection. The objective of the study was to determine IFN-[gamma] responses for the detection of latent tuberculosis infection (LTBI) with Q...
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description | Individuals infected with human immunodeficiency virus (HIV) have an increased risk of progression to active tuberculosis following Mycobacterium tuberculosis infection. The objective of the study was to determine IFN-[gamma] responses for the detection of latent tuberculosis infection (LTBI) with QuantiFERON-TB GOLD In Tube (QFT-G-IT) and T-SPOT.TB in HIV patients, and evaluate the influence of CD4 cell count on tests performance. We studied 75 HIV patients enrolled for ongoing studies of LTBI with T-SPOT.TB, QFN-G-IT and TST. Mean CD4 cell counts [+ -] standard deviation was 461.29 [+ -] 307.49 cells/[mu]l. Eight patients had a BCG scar. T-SPOT.TB, QFN-G-IT and TST were positive in 7 (9.3%), 5 (6.7%) and 9 (12%) cases, respectively. Global agreement between QFN-G-IT and T-SPOT.TB was 89% ([kappa] = 0.275). The overall agreement of T-SPOT.TB and QFN-G-IT with TST was 80.8% ([kappa] = 0.019) and 89% ([kappa] = 0.373), respectively. We have found negative IFN-[gamma] assays results among 2 BCG-vaccinated HIV-infected individuals with a positive TST. In non BCG-vaccinated patients, QFN-G-IT and TST were positive in 5 cases (7.5%) and T-SPOT.TB in 7 (10.4%). In contrast, in BCG-vaccinated patients, only TST was positive in 4/8 (50%) of the cases. The differences obtained in the number of positive results between TST and both IFN-[gamma] assays in BCG vaccinated patients were significant (95% CI 3-97%, p = 0.046), however, the confidence interval is very wide given the small number of patients. In patients with CD4[less than] 200, we obtained only one (5%) positive result with T-SPOT.TB; however, QFN-G-IT and TST were negative in all cases. On the contrary, percentages of positive results in patients with CD4> 200 were 10.9% (6/55), 9.1% (5/55) and 16.4% (9/55) with T-SPOT.TB, QFN-G-IT and TST, respectively. IFN-[gamma] tests have the benefit over TST that are less influenced by BCG vaccination, consequently they are more specific than TST. Although our number of patients with advance immunosuppression is limited, our study suggests that IFN-[gamma] assays are influenced with level of immunosuppression. The use of IFN-[gamma] assays could be a helpful method for diagnosing LTBI in HIV population. |
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The objective of the study was to determine IFN-[gamma] responses for the detection of latent tuberculosis infection (LTBI) with QuantiFERON-TB GOLD In Tube (QFT-G-IT) and T-SPOT.TB in HIV patients, and evaluate the influence of CD4 cell count on tests performance. We studied 75 HIV patients enrolled for ongoing studies of LTBI with T-SPOT.TB, QFN-G-IT and TST. Mean CD4 cell counts [+ -] standard deviation was 461.29 [+ -] 307.49 cells/[mu]l. Eight patients had a BCG scar. T-SPOT.TB, QFN-G-IT and TST were positive in 7 (9.3%), 5 (6.7%) and 9 (12%) cases, respectively. Global agreement between QFN-G-IT and T-SPOT.TB was 89% ([kappa] = 0.275). The overall agreement of T-SPOT.TB and QFN-G-IT with TST was 80.8% ([kappa] = 0.019) and 89% ([kappa] = 0.373), respectively. We have found negative IFN-[gamma] assays results among 2 BCG-vaccinated HIV-infected individuals with a positive TST. In non BCG-vaccinated patients, QFN-G-IT and TST were positive in 5 cases (7.5%) and T-SPOT.TB in 7 (10.4%). In contrast, in BCG-vaccinated patients, only TST was positive in 4/8 (50%) of the cases. The differences obtained in the number of positive results between TST and both IFN-[gamma] assays in BCG vaccinated patients were significant (95% CI 3-97%, p = 0.046), however, the confidence interval is very wide given the small number of patients. In patients with CD4[less than] 200, we obtained only one (5%) positive result with T-SPOT.TB; however, QFN-G-IT and TST were negative in all cases. On the contrary, percentages of positive results in patients with CD4> 200 were 10.9% (6/55), 9.1% (5/55) and 16.4% (9/55) with T-SPOT.TB, QFN-G-IT and TST, respectively. IFN-[gamma] tests have the benefit over TST that are less influenced by BCG vaccination, consequently they are more specific than TST. Although our number of patients with advance immunosuppression is limited, our study suggests that IFN-[gamma] assays are influenced with level of immunosuppression. The use of IFN-[gamma] assays could be a helpful method for diagnosing LTBI in HIV population.</description><identifier>ISSN: 1471-2334</identifier><identifier>EISSN: 1471-2334</identifier><identifier>DOI: 10.1186/1471-2334-10-348</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>CD4 lymphocytes ; Demographic aspects ; Diagnosis ; Dosage and administration ; HIV ; HIV patients ; Human immunodeficiency virus ; Immune response ; Interferon gamma ; Medical research ; Physiological aspects ; Studies ; Tuberculosis</subject><ispartof>BMC infectious diseases, 2010-12, Vol.10, p.348</ispartof><rights>COPYRIGHT 2010 BioMed Central Ltd.</rights><rights>2010 Latorre et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Latorre, Irene</creatorcontrib><creatorcontrib>Martinez-Lacasa, Xavier</creatorcontrib><creatorcontrib>Font, Roser</creatorcontrib><creatorcontrib>Lacoma, Alicia</creatorcontrib><creatorcontrib>Puig, Jordi</creatorcontrib><creatorcontrib>Tural, Cristina</creatorcontrib><creatorcontrib>Lite, Josep</creatorcontrib><creatorcontrib>Prat, Cristina</creatorcontrib><creatorcontrib>Cuchi, Eva</creatorcontrib><creatorcontrib>Ausina, Vicente</creatorcontrib><creatorcontrib>Domínguez, Jose</creatorcontrib><title>IFN-[gamma] response on T-cell based assays in HIV-infected patients for detection of tuberculosis infection</title><title>BMC infectious diseases</title><description>Individuals infected with human immunodeficiency virus (HIV) have an increased risk of progression to active tuberculosis following Mycobacterium tuberculosis infection. The objective of the study was to determine IFN-[gamma] responses for the detection of latent tuberculosis infection (LTBI) with QuantiFERON-TB GOLD In Tube (QFT-G-IT) and T-SPOT.TB in HIV patients, and evaluate the influence of CD4 cell count on tests performance. We studied 75 HIV patients enrolled for ongoing studies of LTBI with T-SPOT.TB, QFN-G-IT and TST. Mean CD4 cell counts [+ -] standard deviation was 461.29 [+ -] 307.49 cells/[mu]l. Eight patients had a BCG scar. T-SPOT.TB, QFN-G-IT and TST were positive in 7 (9.3%), 5 (6.7%) and 9 (12%) cases, respectively. Global agreement between QFN-G-IT and T-SPOT.TB was 89% ([kappa] = 0.275). The overall agreement of T-SPOT.TB and QFN-G-IT with TST was 80.8% ([kappa] = 0.019) and 89% ([kappa] = 0.373), respectively. We have found negative IFN-[gamma] assays results among 2 BCG-vaccinated HIV-infected individuals with a positive TST. In non BCG-vaccinated patients, QFN-G-IT and TST were positive in 5 cases (7.5%) and T-SPOT.TB in 7 (10.4%). In contrast, in BCG-vaccinated patients, only TST was positive in 4/8 (50%) of the cases. The differences obtained in the number of positive results between TST and both IFN-[gamma] assays in BCG vaccinated patients were significant (95% CI 3-97%, p = 0.046), however, the confidence interval is very wide given the small number of patients. In patients with CD4[less than] 200, we obtained only one (5%) positive result with T-SPOT.TB; however, QFN-G-IT and TST were negative in all cases. On the contrary, percentages of positive results in patients with CD4> 200 were 10.9% (6/55), 9.1% (5/55) and 16.4% (9/55) with T-SPOT.TB, QFN-G-IT and TST, respectively. IFN-[gamma] tests have the benefit over TST that are less influenced by BCG vaccination, consequently they are more specific than TST. Although our number of patients with advance immunosuppression is limited, our study suggests that IFN-[gamma] assays are influenced with level of immunosuppression. The use of IFN-[gamma] assays could be a helpful method for diagnosing LTBI in HIV population.</description><subject>CD4 lymphocytes</subject><subject>Demographic aspects</subject><subject>Diagnosis</subject><subject>Dosage and administration</subject><subject>HIV</subject><subject>HIV patients</subject><subject>Human immunodeficiency virus</subject><subject>Immune response</subject><subject>Interferon gamma</subject><subject>Medical research</subject><subject>Physiological aspects</subject><subject>Studies</subject><subject>Tuberculosis</subject><issn>1471-2334</issn><issn>1471-2334</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpNj81LAzEQxYMoWKt3j0HP0Xya5FiK_YCil8WLyJJsJ2XLdlM32YP_vZGKeJrhze_Nm0HoltEHxszTI5OaES6EJIwSIc0ZmvxJ5__6S3SV0p5Spg23E9StFy_kfecOB_eBB0jH2CfAsccVaaDrsHcJttil5L4Sbnu8Wr-Rtg_Q5CIfXW6hzwmHOOAt5KK2xRoDzqOHoRm7mNofWzhNrtFFcF2Cm986RdXiuZqvyOZ1uZ7PNmSnlCJOGksp5dZuZbCKgjYyGMd00EZYZbyXynMvnSpfKM44Y144K5lRAI0FMUV3p7XHIX6OkHK9j-PQl8Ta0kILS1WB7k_QznVQlxNjHlxzaFNTz7hURmiqqfgGrs1kZQ</recordid><startdate>20101210</startdate><enddate>20101210</enddate><creator>Latorre, Irene</creator><creator>Martinez-Lacasa, Xavier</creator><creator>Font, Roser</creator><creator>Lacoma, Alicia</creator><creator>Puig, Jordi</creator><creator>Tural, Cristina</creator><creator>Lite, Josep</creator><creator>Prat, Cristina</creator><creator>Cuchi, Eva</creator><creator>Ausina, Vicente</creator><creator>Domínguez, Jose</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>3V.</scope><scope>7QL</scope><scope>7T2</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20101210</creationdate><title>IFN-[gamma] response on T-cell based assays in HIV-infected patients for detection of tuberculosis infection</title><author>Latorre, Irene ; Martinez-Lacasa, Xavier ; Font, Roser ; Lacoma, Alicia ; Puig, Jordi ; Tural, Cristina ; Lite, Josep ; Prat, Cristina ; Cuchi, Eva ; Ausina, Vicente ; Domínguez, Jose</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g555-a489000299d4f950e784f8a17f783958bb45b2b4a5001521211b3a94185eec9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>CD4 lymphocytes</topic><topic>Demographic aspects</topic><topic>Diagnosis</topic><topic>Dosage and administration</topic><topic>HIV</topic><topic>HIV patients</topic><topic>Human immunodeficiency virus</topic><topic>Immune response</topic><topic>Interferon gamma</topic><topic>Medical research</topic><topic>Physiological aspects</topic><topic>Studies</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Latorre, Irene</creatorcontrib><creatorcontrib>Martinez-Lacasa, Xavier</creatorcontrib><creatorcontrib>Font, Roser</creatorcontrib><creatorcontrib>Lacoma, Alicia</creatorcontrib><creatorcontrib>Puig, Jordi</creatorcontrib><creatorcontrib>Tural, Cristina</creatorcontrib><creatorcontrib>Lite, Josep</creatorcontrib><creatorcontrib>Prat, Cristina</creatorcontrib><creatorcontrib>Cuchi, Eva</creatorcontrib><creatorcontrib>Ausina, Vicente</creatorcontrib><creatorcontrib>Domínguez, Jose</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>BMC infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Latorre, Irene</au><au>Martinez-Lacasa, Xavier</au><au>Font, Roser</au><au>Lacoma, Alicia</au><au>Puig, Jordi</au><au>Tural, Cristina</au><au>Lite, Josep</au><au>Prat, Cristina</au><au>Cuchi, Eva</au><au>Ausina, Vicente</au><au>Domínguez, Jose</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IFN-[gamma] response on T-cell based assays in HIV-infected patients for detection of tuberculosis infection</atitle><jtitle>BMC infectious diseases</jtitle><date>2010-12-10</date><risdate>2010</risdate><volume>10</volume><spage>348</spage><pages>348-</pages><issn>1471-2334</issn><eissn>1471-2334</eissn><abstract>Individuals infected with human immunodeficiency virus (HIV) have an increased risk of progression to active tuberculosis following Mycobacterium tuberculosis infection. The objective of the study was to determine IFN-[gamma] responses for the detection of latent tuberculosis infection (LTBI) with QuantiFERON-TB GOLD In Tube (QFT-G-IT) and T-SPOT.TB in HIV patients, and evaluate the influence of CD4 cell count on tests performance. We studied 75 HIV patients enrolled for ongoing studies of LTBI with T-SPOT.TB, QFN-G-IT and TST. Mean CD4 cell counts [+ -] standard deviation was 461.29 [+ -] 307.49 cells/[mu]l. Eight patients had a BCG scar. T-SPOT.TB, QFN-G-IT and TST were positive in 7 (9.3%), 5 (6.7%) and 9 (12%) cases, respectively. Global agreement between QFN-G-IT and T-SPOT.TB was 89% ([kappa] = 0.275). The overall agreement of T-SPOT.TB and QFN-G-IT with TST was 80.8% ([kappa] = 0.019) and 89% ([kappa] = 0.373), respectively. We have found negative IFN-[gamma] assays results among 2 BCG-vaccinated HIV-infected individuals with a positive TST. In non BCG-vaccinated patients, QFN-G-IT and TST were positive in 5 cases (7.5%) and T-SPOT.TB in 7 (10.4%). In contrast, in BCG-vaccinated patients, only TST was positive in 4/8 (50%) of the cases. The differences obtained in the number of positive results between TST and both IFN-[gamma] assays in BCG vaccinated patients were significant (95% CI 3-97%, p = 0.046), however, the confidence interval is very wide given the small number of patients. In patients with CD4[less than] 200, we obtained only one (5%) positive result with T-SPOT.TB; however, QFN-G-IT and TST were negative in all cases. On the contrary, percentages of positive results in patients with CD4> 200 were 10.9% (6/55), 9.1% (5/55) and 16.4% (9/55) with T-SPOT.TB, QFN-G-IT and TST, respectively. IFN-[gamma] tests have the benefit over TST that are less influenced by BCG vaccination, consequently they are more specific than TST. Although our number of patients with advance immunosuppression is limited, our study suggests that IFN-[gamma] assays are influenced with level of immunosuppression. The use of IFN-[gamma] assays could be a helpful method for diagnosing LTBI in HIV population.</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><doi>10.1186/1471-2334-10-348</doi><oa>free_for_read</oa></addata></record> |
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subjects | CD4 lymphocytes Demographic aspects Diagnosis Dosage and administration HIV HIV patients Human immunodeficiency virus Immune response Interferon gamma Medical research Physiological aspects Studies Tuberculosis |
title | IFN-[gamma] response on T-cell based assays in HIV-infected patients for detection of tuberculosis infection |
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