ArticleJournal of clinical laboratory analysis2009
Cellular immune response profile in patients with American tegumentary leishmaniasis prior and post chemotherapy treatment.
Article in Journal of clinical laboratory analysis, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 26 citations in OpenAlex.
- Immunotherapy Using Immunogenic Mimotopes Selected by Phage Display plus Amphotericin B Inducing a Therapeutic Response in Mice Infected withPathogens (Basel, Switzerland) · 2023Article
- Article
- Regulatory T-Cell Dynamics in Cutaneous and Mucocutaneous Leishmaniasis due toThe American journal of tropical medicine and hygiene · 2018Article
- The Immunology of a Healing Response in Cutaneous Leishmaniasis Treated with Localized Heat or Systemic Antimonial Therapy.PLoS neglected tropical diseases · 2015Article
- The role of inflammatory, anti-inflammatory, and regulatory cytokines in patients infected with cutaneous leishmaniasis in Amazonas State, Brazil.Journal of immunology research · 2014Article
- Immunity to visceral leishmaniasis using genetically defined live-attenuated parasites.Journal of tropical medicine · 2012Article
- CD8+ T cells as a source of IFN-γ production in human cutaneous leishmaniasis.PLoS neglected tropical diseases · 2010Article
- Montenegro skin test and age of skin lesion as predictors of treatment failure in cutaneous leishmaniasis.Revista do Instituto de Medicina Tropical de Sao PauloObservational
- Histopathological and immunohistochemical aspects of American cutaneous leishmaniasis before and after different treatments.Anais brasileiros de dermatologiaArticle
- OX40+ T lymphocytes and IFN-γ are associated with American tegumentary leishmaniasis pathogenesis.Anais brasileiros de dermatologiaArticle
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this study, we have the objective of evaluating the lymphoproliferative response and determining interferon (IFN)-gamma and interleukin (IL)-10 cytokine production in the peripheral blood mononuclear cells (PBMC) of patients with American tegumentary leishmaniasis prior and post 12 months of chemotherapy treatment with meglumine antimoniate compared with the PBMC of noninfected donors. Lymphoproliferation, such as cytokine production, was evaluated through in vitro stimulus with the soluble antigenic fraction from Leishmania (Viannia) braziliensis promastigotes (1.25 microg/ml) and Concanavalin A (2.5 microg/ml). Patients showed a significant lymphoproliferative response prior and post treatment compared with the control group. Similar result, prior to chemotherapy treatment, was observed in IFN-gamma and IL-10 production when patients were compared with the control group. After chemotherapy treatment, PBMC lymphoproliferative response of the patients revealed an increase, whereas patients have shown a decrease in IFN-gamma levels and an increase in IL-10, although without statistical difference. These results may indicate that the patients produced a specific cellular response to the soluble antigenic fraction suggesting that besides Th1 and Th2 dichotomy, immunological regulation mechanisms with the participation of memory T cells and regulatory T cells could be present in the clinical evolution of these patients. This understanding will allow the study and identification of new L. (V.) braziliensis molecules potentially candidates to vaccines.
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