Literature DB >> 29256263

IL-17 and related cytokines involved in systemic sclerosis: Perspectives.

Rafaela Silva Guimarães Gonçalves1,2, Michelly C Pereira2, Andréa Tavares Dantas1,2, Anderson Rodrigues de Almeida2, Claudia Diniz Lopes Marques1, Moacyr J B M Rego2, Ivan R Pitta2, Angela Luzia Branco Pinto Duarte1,2, Maira Galdino R Pitta2.   

Abstract

Systemic sclerosis (SSc) is a multisystemic, complex, and rare disease of connective tissue, with high morbidity and mortality, and without specific treatment. The disease is characterized by three main principles: vascular disease, autoantibody production and inflammation, and fibrosis. Since it is well defined that SSc is characterized by elevated production of TGF-β, IL-6, and IL-1, all of them cytokines related to Th17 differentiation, the hypothesis is that this disease may be strongly related to a polarization of the immune response towards the Th17 pathway. Considering the importance of a better understanding of the pathophysiology of Th17 pathway in SSc, this article aims to propose an update for a better understanding of current knowledge on main cytokines secreted by the Th17 cells (IL-17 A, IL-21, and IL-22) and the future prospects in the current disease.

Entities:  

Keywords:  CD4(+) T cells; Th17 cells; fibroblasts; fibrosis

Mesh:

Substances:

Year:  2017        PMID: 29256263     DOI: 10.1080/08916934.2017.1416467

Source DB:  PubMed          Journal:  Autoimmunity        ISSN: 0891-6934            Impact factor:   2.815


  13 in total

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10.  Semaphorin4A-Plexin D1 Axis Induces Th2 and Th17 While Represses Th1 Skewing in an Autocrine Manner.

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