Literature DB >> 25115057

The role of toll-like receptor agonists in the immunotherapy of leishmaniosis. An update and proposal for a new form of anti-leishmanial therapy.

Subhajit Dasgupta, Sanaz Aghazadeh-Dibavar, Mausumi Bandyopadyay.   

Abstract

The use of toll-like receptor agonists in immunotherapy is a new approach in the prevention of immunosuppression during fatal Leishmania parasite infection. The objective of such immunotherapy is to activate specific cell-mediated immune responses, macrophage activation and antigen-responsive inflammation, to kill intracellular amastigotes. Toll-like receptor agonist-based treatment in immunocompetent hosts can be effective either by selective use of the agonists alone or in combination with the anti-leishmanial drug stibanate. Recent investigations suggest that toll-like receptor signal pathways constitute a possible new mode of anti-leishmanial treatment. This article describes the prospect of toll-like receptor - mediated signal pathways in the immunotherapy of cutaneous and visceral leishmaniosis, as well as post kala-azar dermal leishmaniosis (PKADL), a skin-sequel of visceral infection. Suitable synthetic agonists need to be developed for toll-like receptors to overcome immunosuppression.

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Year:  2014        PMID: 25115057

Source DB:  PubMed          Journal:  Ann Parasitol        ISSN: 2299-0631


  3 in total

Review 1.  Genome mining offers a new starting point for parasitology research.

Authors:  Zhiyue Lv; Zhongdao Wu; Limei Zhang; Pengyu Ji; Yifeng Cai; Shiqi Luo; Hongxi Wang; Hao Li
Journal:  Parasitol Res       Date:  2015-01-08       Impact factor: 2.289

2.  A new multi-epitope peptide vaccine induces immune responses and protection against Leishmania infantum in BALB/c mice.

Authors:  Bahareh Vakili; Navid Nezafat; Bijan Zare; Nasrollah Erfani; Maryam Akbari; Younes Ghasemi; Mohammad Reza Rahbar; Gholam Reza Hatam
Journal:  Med Microbiol Immunol       Date:  2019-11-06       Impact factor: 3.402

3.  CD14 is critical for TLR2-mediated M1 macrophage activation triggered by N-glycan recognition.

Authors:  Thiago Aparecido da Silva; André L V Zorzetto-Fernandes; Nerry T Cecílio; Aline Sardinha-Silva; Fabrício Freitas Fernandes; Maria Cristina Roque-Barreira
Journal:  Sci Rep       Date:  2017-08-01       Impact factor: 4.379

  3 in total

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