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Regulatory T-Cell Profile in Early and Late Lesions of Cutaneous Leishmaniasis Due to Leishmania Major



Hoseini SG1 ; Javanmard SH3 ; Zarkesh SH2 ; Khamesipour A6 ; Rafiei L2 ; Karbalaie K4 ; Nilforoushzade M5 ; Baghaei M7 ; Hejazi SH1
Authors
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Authors Affiliations
  1. 1. Department of Parasitology and Mycology, Skin Diseases and Leishmaniasis Research Center, Isfahan, Iran
  2. 2. Department of Immunology, School of Medicine, Isfahan, Iran
  3. 3. Department of Physiology, Physiology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Department of Cell and Molecular Biology, Cell Science Research Center, Royan Institute for Animal Biotechnology, ACECR, Isfahan, Iran
  5. 5. Skin and Stem Cell Research Center, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Center for Research in Skin Disease and Leprosy, Tehran, Iran
  7. 7. Department of Biology, Faculty of Basic Sciences Islamic Azad University Shahrekord Branch, Shrekord, Iran

Source: Journal of Research in Medical Sciences Published:2012

Abstract

Context: Cutaneous leishmaniasis (CL) is a public health problem in several endemic countries. Recent studies on mouse model and also a few clinical experiments showed that the type of immune response generated at the site of infection and especially balance between regulatory and effector T-cells determines the outcome of the disease toward self-limiting or long-lasting lesions. Aims: The aim of this study was to evaluate the role of natural regulatory T cells (nTregs) in early and late cutaneous lesions of human Leishmania major (L. major) infection. Settings and Design: Skin biopsies were collected from parasitologically proven lesions of 28 CL patients, divided into two groups of early and late lesions. The causative agents were identified to be L. major. Materials and Methods: Quantitative real-time reverse transcription polymerase chain reaction (PCR) and immunofluorescent staining of biopsies were used to assess the Foxp3 mRNA expression and frequency of nTregs in two groups. Mann-Whitney U test was used to determine the significance of deference between the two groups. Results: Mean relative expressions of Foxp3 mRNA were 0.53 ± 0.23 and 1.26 ± 0.99 in early and late lesions, respectively, which was significantly upper in chronic lesions (P = 0.007). Parallel results were obtained in tissue staining method. Conclusions: Increased in gene expression and protein staining of nTreg markers in chronic biopsy samples indicates a role for these cells in chronic L. major induced leishmaniasis and supports the effectiveness of regulatory T cell-based immunotherapy for treatment of chronic CL.
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