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Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing
Interferon (IFN)-γ release assays (IGRA) have improved tuberculosis contact tracing, but discrimination of recent from remote Mycobacterium tuberculosis contacts is not possible by IGRA alone. We present results of a tuberculosis contact investigation with a new early-secretory-antigenic-target (ESA...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907387/ https://www.ncbi.nlm.nih.gov/pubmed/20652022 http://dx.doi.org/10.1371/journal.pone.0011670 |
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author | Krummel, Benjamin Strassburg, Alan Ernst, Martin Reiling, Norbert Eker, Barbara Rath, Heidrun Hoerster, Robert Wappler, Waltraud Glaewe, Andrea Schoellhorn, Volker Sotgiu, Giovanni Lange, Christoph |
author_facet | Krummel, Benjamin Strassburg, Alan Ernst, Martin Reiling, Norbert Eker, Barbara Rath, Heidrun Hoerster, Robert Wappler, Waltraud Glaewe, Andrea Schoellhorn, Volker Sotgiu, Giovanni Lange, Christoph |
author_sort | Krummel, Benjamin |
collection | PubMed |
description | Interferon (IFN)-γ release assays (IGRA) have improved tuberculosis contact tracing, but discrimination of recent from remote Mycobacterium tuberculosis contacts is not possible by IGRA alone. We present results of a tuberculosis contact investigation with a new early-secretory-antigenic-target (ESAT)-6 and culture-filtrate-protein (CFP)-10 specific interleukin (IL)-2 ELISpot in addition to ESAT-6 and CFP-10 specific IFN-γ ELISpot and tuberculin skin testing (TST). Results of the TST, IFN-γ ELISpot and IL-2 ELISpot were positive in 6/172 (3.4%), 7/167 (4.2%) and 6/196 (3.1%) of contacts, respectively. Close contact (≥100 hours) to the index case increased the risk of positive results in the IFN-γ ELISpot, TST, and IL-2 ELISpot by 40.8, 19.3, and 2.5 times, respectively. Individuals with a positive IFN-γ ELISpot/negative IL-2 ELISpot result had a median (IQR) duration of index case exposure of 568 hours (133_1000) compared to individuals with a positive IFN-γ ELISpot/positive IL-2 ELISpot result (median = 24 hours; 20_130; p-value = 0.047). Combination of a M. tuberculosis specific IFN-γ ELISpot with a M. tuberculosis specific IL-2 ELISpot significantly improved the identification of individuals with the highest risk of recent M. tuberculosis infection and is a promising method that should be explored to target tuberculosis preventive chemotherapy. |
format | Text |
id | pubmed-2907387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29073872010-07-22 Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing Krummel, Benjamin Strassburg, Alan Ernst, Martin Reiling, Norbert Eker, Barbara Rath, Heidrun Hoerster, Robert Wappler, Waltraud Glaewe, Andrea Schoellhorn, Volker Sotgiu, Giovanni Lange, Christoph PLoS One Research Article Interferon (IFN)-γ release assays (IGRA) have improved tuberculosis contact tracing, but discrimination of recent from remote Mycobacterium tuberculosis contacts is not possible by IGRA alone. We present results of a tuberculosis contact investigation with a new early-secretory-antigenic-target (ESAT)-6 and culture-filtrate-protein (CFP)-10 specific interleukin (IL)-2 ELISpot in addition to ESAT-6 and CFP-10 specific IFN-γ ELISpot and tuberculin skin testing (TST). Results of the TST, IFN-γ ELISpot and IL-2 ELISpot were positive in 6/172 (3.4%), 7/167 (4.2%) and 6/196 (3.1%) of contacts, respectively. Close contact (≥100 hours) to the index case increased the risk of positive results in the IFN-γ ELISpot, TST, and IL-2 ELISpot by 40.8, 19.3, and 2.5 times, respectively. Individuals with a positive IFN-γ ELISpot/negative IL-2 ELISpot result had a median (IQR) duration of index case exposure of 568 hours (133_1000) compared to individuals with a positive IFN-γ ELISpot/positive IL-2 ELISpot result (median = 24 hours; 20_130; p-value = 0.047). Combination of a M. tuberculosis specific IFN-γ ELISpot with a M. tuberculosis specific IL-2 ELISpot significantly improved the identification of individuals with the highest risk of recent M. tuberculosis infection and is a promising method that should be explored to target tuberculosis preventive chemotherapy. Public Library of Science 2010-07-20 /pmc/articles/PMC2907387/ /pubmed/20652022 http://dx.doi.org/10.1371/journal.pone.0011670 Text en Krummel et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Krummel, Benjamin Strassburg, Alan Ernst, Martin Reiling, Norbert Eker, Barbara Rath, Heidrun Hoerster, Robert Wappler, Waltraud Glaewe, Andrea Schoellhorn, Volker Sotgiu, Giovanni Lange, Christoph Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title | Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title_full | Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title_fullStr | Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title_full_unstemmed | Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title_short | Potential Role for IL-2 ELISpot in Differentiating Recent and Remote Infection in Tuberculosis Contact Tracing |
title_sort | potential role for il-2 elispot in differentiating recent and remote infection in tuberculosis contact tracing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907387/ https://www.ncbi.nlm.nih.gov/pubmed/20652022 http://dx.doi.org/10.1371/journal.pone.0011670 |
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