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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Veröffentlicht in:BMC infectious diseases 2010-12, Vol.10, p.348
Hauptverfasser: Latorre, Irene, Martinez-Lacasa, Xavier, Font, Roser, Lacoma, Alicia, Puig, Jordi, Tural, Cristina, Lite, Josep, Prat, Cristina, Cuchi, Eva, Ausina, Vicente, Domínguez, Jose
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container_title BMC infectious diseases
container_volume 10
creator Latorre, Irene
Martinez-Lacasa, Xavier
Font, Roser
Lacoma, Alicia
Puig, Jordi
Tural, Cristina
Lite, Josep
Prat, Cristina
Cuchi, Eva
Ausina, Vicente
Domínguez, Jose
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&gt; 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. 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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&gt; 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. 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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&gt; 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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source Springer Nature - Complete Springer Journals; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access; Springer Nature OA Free Journals
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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