alexa Thymus Output of CD4+CD25highTreg+ is Increased in Patients Carrying Leprae Disease
ISSN: 2155-9554

Journal of Clinical & Experimental Dermatology Research
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Research Article

Thymus Output of CD4+CD25highTreg+ is Increased in Patients Carrying Leprae Disease

Bruna Luisa Figueirêdo Pierote1, Ester Miranda Pereira1, Semiramis Jamil Hadad do Monte1, Rubens de Sousa Santana1, Deylane Menezes Teles e Oliveira1, Saara Barros Nascimento1 and Adalberto Socorro da Silva1,2*

1Immunogenetics and molecular biology laboratory, Federal university of Piauí-Brazil

2Department of biological sciences, Nature Science Center (CCN), Federal university of Piauí-Brazil

*Corresponding Author:
Adalberto Socorro da Silva
Immunogenetics and molecular biology laboratory
Federal university of Piauí-Brazil
Tel: +55 86 32155691
Fax: +55 86 32155690
E-mail: [email protected]

Received date: July 15, 2015 Accepted date: December 11, 2015 Published date: December 20, 2015

Citation: Figueirêdo Pierote BS, Pereira EM, Hadad do Monte SJ, Sousa Santana RD, Teles e Oliveira DM et al. (2015) Thymus Output of CD4+CD25highTreg+ is Increased in Patients Carrying Leprae Disease. J Clin Exp Dermatol Res 7:316. doi: 10.4172/2155-9554.1000316

Copyright: © 2015 Figueirêdo Pierote BL. et al., 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 credited.

 

Abstract

Background: Leprosy is an infectious disease caused by the intracellular pathogen Mycobacterium leprae, which is a microorganism that evades the host’s immune response. The mechanisms regulating immune circumvention are not fully understood. It has been proposed that the pathogen alters the mechanisms regulating the immune response of the host to escape immune surveillance. Thus, regulatory T cells are important immune elements that must be investigated. To escape the immune response using regulatory properties or natural regulatory T cells (nTreg), M. leprae increases the number of nTregs observed in the steady-state. Because nTregs are thymus derived, one way to verify if M. leprae infection induces de novo nTreg cells is to determine the nature of recent thymus emigrant nTregs in leprosy patients and compare the cells to healthy controls. Objectives: In this study, we (i) quantified the regulatory T cells in the peripheral blood of leprosy patients compared to healthy age-matched controls, (ii) determined whether these cells show a phenotype of recent thymic emigrants, and (iii) evaluated the cytokine profile in plasma samples. All of the studies were performed using flow cytometry. Results: We found higher levels of nTreg cells during early periods of the disease. Additionally, there was a continuous decrease in nTreg cells throughout the treatment. Moreover, the nTregs were recent thymic emigrants, as shown by the expression of a specific marker (PTK7).We did not find any difference in the cytokine profile when comparing patients and controls. Conclusion: The levels of CD4+CD25highFoxp3+ T cells in patients with leprosy are most likely evidence of thymic output. In addition, blood levels of CD4+CD25highFoxp3+PtK7+ can be used to monitor treatment progress in leprosy.

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