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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/11986

Title: Analysis of Mycobacterium ulcerans-specific Tcell cytokines for diagnosis of Buruli ulcer disease and as potential indicator for disease progression
Authors: Nausch, Norman
Antwi-Berko, Daniel
Mubarik, Yusif
Abass, Kabiru Mohammed
Owusu, Wellington
Owusu-Dabo, Ellis
Debrah, Linda Batsa
Debrah, A. Y
Jacobsen, Marc
Phillips, Richard O.
Issue Date: Feb-2017
Publisher: PLoS Neglected Tropical Diseases
Citation: PLoS Neglected Tropical Diseases 11(2):e0005415
Abstract: Background Buruli ulcer disease (BUD), caused by Mycobacterium (M.) ulcerans, is the third most common mycobacterial disease after tuberculosis and leprosy. BUD causes necrotic skin lesions and is a significant problem for health care in the affected countries. As for other mycobacterial infections, T cell mediated immune responses are important for protection and recovery during treatment, but detailed studies investigating these immune responses in BUD patients are scarce. In this study, we aimed to characterise M. ulcerans-specific CD4+ T cell responses in BUD patients and to analyse specific cytokine-producing T cells in the context of disease severity and progression. Methodology/Principal findings For this case-control study, whole blood samples of BUD patients (N = 36, 1.5?17 years of age) and healthy contacts (N = 22, 3?15 years of age) were stimulated with antigen prepared from M. ulcerans and CD4+ T cells were analysed for the expression of TNF?, IFN? and CD40L by flow cytometry. The proportions and profile of cytokine producing CD4+ T cells was compared between the two study groups and correlated with disease progression and severity. Proportions of cytokine double-positive IFN?+TNF?+, TNF?+CD40L+, IFN?+CD40L+ (p = 0.014, p = 0.010, p = 0.002, respectively) and triple positive IFN?+TNF?+CD40L+ (p = 0.010) producing CD4+ T cell subsets were increased in BUD patients. In addition, TNF?+CD40L-IFN?- CD4+ T cells differed between patients and controls (p = 0.034). TNF?+CD40L-IFN?- CD4+ T cells were correlated with lesion size (p = 0.010) and proportion were higher in ?slow? healers compared to ?fast healers? (p = 0.030). Conclusions We were able to identify M. ulcerans-specific CD4+ T cell subsets with specific cytokine profiles. In particular a CD4+ T cell subset, producing TNF? but not IFN? and CD40L, showed association with lesion size and healing progress. Further studies are required to investigate, if the identified CD4+ T cell subset has the potential to be used as biomarker for diagnosis, severity and/or progression of disease.
Description: This article is published in PLoS Neglected Tropical Diseasesand aslo available at DOI: 10.1371/journal.pntd.0005415
URI: 10.1371/journal.pntd.0005415
http://hdl.handle.net/123456789/11986
Appears in Collections:College of Health Sciences

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