Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients

Measurements of antigen-specific T cell responses in chronic diseases are limited by low frequencies of antigen-specific cells in the peripheral blood. Therefore, attempts have been made to add costimulatory molecules such as anti-CD28 or IL-7/IL-15 to ELISPOT assays to increase sensitivity. While...

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Main Authors: Stefanie Kuerten, Tobias R. Schlingmann, Tarvo Rajasalu, Doychin N. Angelov, Paul V. Lehmann, Magdalena Tary-Lehmann
Format: Article
Language:English
Published: Wiley 2008-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2008/590941
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author Stefanie Kuerten
Tobias R. Schlingmann
Tarvo Rajasalu
Doychin N. Angelov
Paul V. Lehmann
Magdalena Tary-Lehmann
author_facet Stefanie Kuerten
Tobias R. Schlingmann
Tarvo Rajasalu
Doychin N. Angelov
Paul V. Lehmann
Magdalena Tary-Lehmann
author_sort Stefanie Kuerten
collection DOAJ
description Measurements of antigen-specific T cell responses in chronic diseases are limited by low frequencies of antigen-specific cells in the peripheral blood. Therefore, attempts have been made to add costimulatory molecules such as anti-CD28 or IL-7/IL-15 to ELISPOT assays to increase sensitivity. While this approach has been successful under certain circumstances, results are often inconsistent. To date, there are no comprehensive studies directly comparing the in vitro effects of multiple costimulatory molecules in different disease settings. Therefore, in the present study we tested the effects of IL-7/IL-15, IFN-α, anti-ICOS, and anti-CD28 on antigen-specific T cell responses in patients infected with HCV or HIV versus healthy individuals. Our data show that none of the aforementioned molecules could significantly increase ELISPOT sensitivity, neither in HCV nor in HIV. Moreover, all of them caused false-positive responses to HCV and HIV antigens in healthy individuals. Our results question the broad use of in vitro costimulation.
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spelling doaj-art-e7cb61565ba64c9b9bef16522915ae952025-02-03T01:09:45ZengWileyClinical and Developmental Immunology1740-25221740-25302008-01-01200810.1155/2008/590941590941Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected PatientsStefanie Kuerten0Tobias R. Schlingmann1Tarvo Rajasalu2Doychin N. Angelov3Paul V. Lehmann4Magdalena Tary-Lehmann5Institut für Anatomie I, Medizinische Fakultät der Universität zu Köln, Joseph-Stelzmann-Str. 9, 50931 Köln, GermanyDepartment of Pathology, Case Western Reserve University, Wolstein Building, 10900 Euclid Avenue, Cleveland, OH 44106, USADepartment of Pathology, Case Western Reserve University, Wolstein Building, 10900 Euclid Avenue, Cleveland, OH 44106, USAInstitut für Anatomie I, Medizinische Fakultät der Universität zu Köln, Joseph-Stelzmann-Str. 9, 50931 Köln, GermanyDepartment of Pathology, Case Western Reserve University, Wolstein Building, 10900 Euclid Avenue, Cleveland, OH 44106, USADepartment of Pathology, Case Western Reserve University, Wolstein Building, 10900 Euclid Avenue, Cleveland, OH 44106, USAMeasurements of antigen-specific T cell responses in chronic diseases are limited by low frequencies of antigen-specific cells in the peripheral blood. Therefore, attempts have been made to add costimulatory molecules such as anti-CD28 or IL-7/IL-15 to ELISPOT assays to increase sensitivity. While this approach has been successful under certain circumstances, results are often inconsistent. To date, there are no comprehensive studies directly comparing the in vitro effects of multiple costimulatory molecules in different disease settings. Therefore, in the present study we tested the effects of IL-7/IL-15, IFN-α, anti-ICOS, and anti-CD28 on antigen-specific T cell responses in patients infected with HCV or HIV versus healthy individuals. Our data show that none of the aforementioned molecules could significantly increase ELISPOT sensitivity, neither in HCV nor in HIV. Moreover, all of them caused false-positive responses to HCV and HIV antigens in healthy individuals. Our results question the broad use of in vitro costimulation.http://dx.doi.org/10.1155/2008/590941
spellingShingle Stefanie Kuerten
Tobias R. Schlingmann
Tarvo Rajasalu
Doychin N. Angelov
Paul V. Lehmann
Magdalena Tary-Lehmann
Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
Clinical and Developmental Immunology
title Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
title_full Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
title_fullStr Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
title_full_unstemmed Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
title_short Lack of Disease Specificity Limits the Usefulness of In Vitro Costimulation in HIV- and HCV-Infected Patients
title_sort lack of disease specificity limits the usefulness of in vitro costimulation in hiv and hcv infected patients
url http://dx.doi.org/10.1155/2008/590941
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