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Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica

PURPOSE: The interaction between the Leishmania parasite and the host cell involves complex, multifaceted processes. The disease severity in cutaneous leishmaniasis (CL) is largely dependent on the causative species. Most of the information on immune responses in human CL is available with respect t...

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Autores principales: Katara, Gajendra Kumar, Raj, Anand, Kumar, Rajesh, Avishek, Kumar, Kaushal, Himanshu, Ansari, Nasim Akhtar, Bumb, Ram Awatar, Salotra, Poonam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840658/
https://www.ncbi.nlm.nih.gov/pubmed/24267152
http://dx.doi.org/10.1186/1471-2172-14-52
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author Katara, Gajendra Kumar
Raj, Anand
Kumar, Rajesh
Avishek, Kumar
Kaushal, Himanshu
Ansari, Nasim Akhtar
Bumb, Ram Awatar
Salotra, Poonam
author_facet Katara, Gajendra Kumar
Raj, Anand
Kumar, Rajesh
Avishek, Kumar
Kaushal, Himanshu
Ansari, Nasim Akhtar
Bumb, Ram Awatar
Salotra, Poonam
author_sort Katara, Gajendra Kumar
collection PubMed
description PURPOSE: The interaction between the Leishmania parasite and the host cell involves complex, multifaceted processes. The disease severity in cutaneous leishmaniasis (CL) is largely dependent on the causative species. Most of the information on immune responses in human CL is available with respect to L. major infection and is lacking for L. tropica species. In this study, we employed cytokine/chemokine/receptor membrane cDNA array to capture comprehensive picture of immuno-determinants in localized human tissue during L. tropica infection. Expression of selected molecules was evaluated by real time PCR in dermal lesion tissues at pre- and post treatment stages. Plasma IL-17 level was estimated by sandwich ELISA. RESULTS: The cDNA array analysis identified several immuno-determinants in tissue lesions of Indian CL including cytokines (IFN-γ, TNF-α, IL-1β, IL-10, IL-13), chemokines (IL-8, CCL2, CCL3, CCL4) and apoptotic molecules (Fas, TRAIL, IRF-1). Elevated mRNA levels of Th17 (IL-17, IL-23 and RORγt) and Treg (CD25, CTLA-4 and Foxp3) markers were observed in lesion tissues of CL patients compared to the control group, which subsided post treatment. Plasma IL-17 levels were found to be significantly higher in CL samples compared to controls. CONCLUSIONS: In addition to defining comprehensive immunological responses inside lesion tissues of CL patients, our study demonstrated the presence of Th17 and Treg cells in CL caused by L. tropica.
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spelling pubmed-38406582013-11-27 Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica Katara, Gajendra Kumar Raj, Anand Kumar, Rajesh Avishek, Kumar Kaushal, Himanshu Ansari, Nasim Akhtar Bumb, Ram Awatar Salotra, Poonam BMC Immunol Research Article PURPOSE: The interaction between the Leishmania parasite and the host cell involves complex, multifaceted processes. The disease severity in cutaneous leishmaniasis (CL) is largely dependent on the causative species. Most of the information on immune responses in human CL is available with respect to L. major infection and is lacking for L. tropica species. In this study, we employed cytokine/chemokine/receptor membrane cDNA array to capture comprehensive picture of immuno-determinants in localized human tissue during L. tropica infection. Expression of selected molecules was evaluated by real time PCR in dermal lesion tissues at pre- and post treatment stages. Plasma IL-17 level was estimated by sandwich ELISA. RESULTS: The cDNA array analysis identified several immuno-determinants in tissue lesions of Indian CL including cytokines (IFN-γ, TNF-α, IL-1β, IL-10, IL-13), chemokines (IL-8, CCL2, CCL3, CCL4) and apoptotic molecules (Fas, TRAIL, IRF-1). Elevated mRNA levels of Th17 (IL-17, IL-23 and RORγt) and Treg (CD25, CTLA-4 and Foxp3) markers were observed in lesion tissues of CL patients compared to the control group, which subsided post treatment. Plasma IL-17 levels were found to be significantly higher in CL samples compared to controls. CONCLUSIONS: In addition to defining comprehensive immunological responses inside lesion tissues of CL patients, our study demonstrated the presence of Th17 and Treg cells in CL caused by L. tropica. BioMed Central 2013-11-22 /pmc/articles/PMC3840658/ /pubmed/24267152 http://dx.doi.org/10.1186/1471-2172-14-52 Text en Copyright © 2013 Katara et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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.
spellingShingle Research Article
Katara, Gajendra Kumar
Raj, Anand
Kumar, Rajesh
Avishek, Kumar
Kaushal, Himanshu
Ansari, Nasim Akhtar
Bumb, Ram Awatar
Salotra, Poonam
Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title_full Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title_fullStr Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title_full_unstemmed Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title_short Analysis of localized immune responses reveals presence of Th17 and Treg cells in cutaneous leishmaniasis due to Leishmania tropica
title_sort analysis of localized immune responses reveals presence of th17 and treg cells in cutaneous leishmaniasis due to leishmania tropica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840658/
https://www.ncbi.nlm.nih.gov/pubmed/24267152
http://dx.doi.org/10.1186/1471-2172-14-52
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