Immuno-metabolic reprogramming of T cell: a new frontier for pharmacotherapy of Rheumatoid arthritis.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Sourav Mondal, Sarthak Saha, Debjeet Sur
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引用次数: 0

Abstract

Rheumatoid arthritis (RA) is a persistent autoimmune condition characterized by ongoing inflammation primarily affecting the synovial joint. This inflammation typically arises from an increase in immune cells such as neutrophils, macrophages, and T cells (TC). TC is recognized as a major player in RA pathogenesis. The involvement of HLA-DRB1 and PTPN-2 among RA patients confirms the TC involvement in RA. Metabolism of TC is maintained by various other factors like cytokines, mitochondrial proteins & other metabolites. Different TC subtypes utilize different metabolic pathways like glycolysis, oxidative phosphorylation and fatty acid oxidation for their activation from naive TC (T0). Although all subsets of TC are not deleterious for synovium, some subsets of TC are involved in joint repair using their anti-inflammatory properties. Hence artificially reprogramming of TC subset by interfering with their metabolic status poised a hope in future to design new molecules against RA.

免疫代谢重编程 T 细胞:类风湿关节炎药物疗法的新前沿。
类风湿性关节炎(RA)是一种持续性自身免疫性疾病,其特征是主要影响滑膜关节的持续炎症。这种炎症通常源于免疫细胞(如中性粒细胞、巨噬细胞和 T 细胞 (TC))的增加。TC被认为是RA发病机制中的主要角色。RA 患者中 HLA-DRB1 和 PTPN-2 的参与证实了 TC 在 RA 中的参与。细胞因子、线粒体蛋白和其他代谢物等各种其他因素维持着 TC 的新陈代谢。不同的 TC 亚型利用不同的代谢途径,如糖酵解、氧化磷酸化和脂肪酸氧化,将其从幼稚 TC(T0)激活。尽管所有 TC 亚型都不会对滑膜造成危害,但某些 TC 亚型会利用其抗炎特性参与关节修复。因此,通过干扰TC亚群的新陈代谢状态对其进行人工重编程,有望在未来设计出对抗RA的新分子。
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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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