| Literature DB >> 29256263 |
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