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Open AccessJournal ArticleDOI

Regulatory T Cells Suppress T Cell Activation at the Pathologic Site of Human Visceral Leishmaniasis

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TLDR
The results suggest that IL-10 plays an important role in suppression of host immunity in human VL and possibly determines the efficacy of chemotherapy.
Abstract
Suppression of T cell response is thought to be involved in the pathogenesis of visceral leishmaniasis (VL). Regulatory T cell (Treg) mediated immune-suppression is reported in animal models of Leishmania infection. However, their precise role among human patients still requires pathologic validation. The present study is aimed at understanding the frequency dynamics and function of Treg cells in the blood and bone marrow (BM) of VL patients. The study included 42 parasitologically confirmed patients, 17 healthy contact and 9 normal bone marrow specimens (NBM). We show i) the selective accumulation of Treg cells at one of the disease inflicted site(s), the BM, ii) their in vitro expansion in response to LD antigen and iii) persistence after successful chemotherapy. Results indicate that the Treg cells isolated from BM produces IL-10 and may inhibit T cell activation in IL-10 dependent manner. Moreover, we observed significantly higher levels of IL-10 among drug unresponsive patients, suggesting their critical role in suppression of immunity among VL patients. Our results suggest that IL-10 plays an important role in suppression of host immunity in human VL and possibly determines the efficacy of chemotherapy.

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Book ChapterDOI

Mechanisms of immune evasion in leishmaniasis.

TL;DR: Immuno-therapeutic approaches that target mechanisms of immune evasion by Leishmania offer promising areas for preclinical and clinical research.
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Immunobiology of visceral leishmaniasis

TL;DR: In this review, immunological events described in human and experimental VL and how these can affect the outcome of infection are discussed.
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Immune regulation during chronic visceral leishmaniasis.

TL;DR: In this article, the authors review recent discoveries in these areas and highlight shortcomings in our knowledge that need to be addressed if better treatment options are to be developed and effective vaccines designed.
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Immunopathogenesis of non-healing American cutaneous leishmaniasis and progressive visceral leishmaniasis.

TL;DR: Recent evidence from human and animal studies is summarized that reveals the mechanisms of dysregulated, hyper-responses to Leishmania braziliensis, as well as the presence of disease-promoting or the absence of protective responses to Leishesmania amazonensis and Leishmaniasis donovani.

Immune regulation during chronic visceral leishmaniasis

TL;DR: There is an urgent need to better understand immune responses following infection with Leishmania species by studying animal models of disease and clinical samples from patients, and recent discoveries are reviewed.
References
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Journal ArticleDOI

Conventional T-bet(+)Foxp3(-) Th1 cells are the major source of host-protective regulatory IL-10 during intracellular protozoan infection.

TL;DR: In this article, the source of regulatory IL-10 in mice infected with the protozoan parasite Toxoplasma gondii was analyzed and it was found that the same IFN-10(+)IFN-gamma(gamma) population displayed potent effector function against the parasite while, paradoxically, also inducing profound suppression of IL-12 production by antigen-presenting cells.
Journal ArticleDOI

CD4+CD25−Foxp3− Th1 cells are the source of IL-10–mediated immune suppression in chronic cutaneous leishmaniasis

TL;DR: It is demonstrated that Th1 cells, activated early in a strong inflammatory setting as a mechanism of feedback control, are the principal mediators of T cell–derived IL-10–dependent immune suppression in a chronic intracellular infection.
Journal ArticleDOI

The Role of IL-10 in Promoting Disease Progression in Leishmaniasis

TL;DR: These studies indicate that amastigotes of Leishmania use an unusual and unexpected virulence factor, host IgG, which allows them to exploit the antiinflammatory effects of FcγR ligation to induce the production of IL-10, which renders macrophages refractory to the activating effects of IFN-γ.
Journal ArticleDOI

Bone marrow is a reservoir for CD4+CD25+ regulatory T cells that traffic through CXCL12/CXCR4 signals.

TL;DR: Findings show a mechanism for homeostatic Treg trafficking and indicate that bone marrow is a significant reservoir for Tregs, and suggest a novel mechanism explaining reduced acute graft-versus-host disease and improvement in autoimmune diseases following G-CSF treatment.
Journal ArticleDOI

Infected site-restricted Foxp3+ natural regulatory T cells are specific for microbial antigens

TL;DR: The results support the idea that natural T reg cells are able to respond specifically to foreign antigens in that they strongly proliferate in response to Leishmania-infected dendritic cells, they maintain Foxp3 expression, and Leishmaniasis-specific T reg cell lines can be generated from infected mice.
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