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Infection and Immunity, November 2006, p. 6317-6323, Vol. 74, No. 11
0019-9567/06/$08.00+0 doi:10.1128/IAI.00890-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
ß and 
T Cells from Human Patients with Cutaneous Leishmaniasis
Department of Biochemistry and Immunology,1 Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil,2 Immunology Service, Hospital Edgard Santos, UFBA, Salvador, Bahia, Brazil3
Received 6 June 2006/ Returned for modification 18 June 2006/ Accepted 11 August 2006
Although most T lymphocytes express the
ß T-cell receptor and either CD4 or CD8 molecules, a small population of cells lacking these coreceptors, CD4 CD8 (double negative [DN]) T cells, has been identified in the peripheral immune system of mice and humans. To better understand the role that this population may have in the human immune response against Leishmania spp., a detailed study defining the activation state, cytokine profile, and the heterogeneity of DN T cells bearing
ß or 
T-cell receptors was performed with a group of well-defined cutaneous leishmaniasis patients. Strikingly, on average 75% of DN T cells from cutaneous leishmaniasis patients expressed the
ß T-cell receptor, with the remainder expressing the 
receptor, while healthy donors displayed the opposite distribution with
75% of the DN T cells expressing the 
T-cell receptor. Additionally,
ß DN T cells from cutaneous leishmaniasis patients are compatible with previous antigen exposure and recent activation. Moreover, while
ß DN T cells from Leishmania-infected individuals present a proinflammatory cytokine profile, 
DN T cells express a regulatory profile exemplified by interleukin-10 production. The balance between these subpopulations could allow for the formation of an effective cellular response while limiting its pathogenic potential.
Published ahead of print on 21 August 2006.
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