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特应性皮炎中的 T 细胞共刺激和共抑制途径。

T cell co-stimulatory and co-inhibitory pathways in atopic dermatitis.

机构信息

Skin and Cosmetic Research Department, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai, China.

Institute of Psoriasis, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai, China.

出版信息

Front Immunol. 2023 Mar 13;14:1081999. doi: 10.3389/fimmu.2023.1081999. eCollection 2023.

Abstract

The use of immune checkpoint inhibitors (ICIs) targeting the T cell inhibitory pathways has revolutionized cancer treatment. However, ICIs might induce progressive atopic dermatitis (AD) by affecting T cell reactivation. The critical role of T cells in AD pathogenesis is widely known. T cell co-signaling pathways regulate T cell activation, where co-signaling molecules are essential for determining the magnitude of the T cell response to antigens. Given the increasing use of ICIs in cancer treatment, a timely overview of the role of T cell co-signaling molecules in AD is required. In this review, we emphasize the importance of these molecules involved in AD pathogenesis. We also discuss the potential of targeting T cell co-signaling pathways to treat AD and present the unresolved issues and existing limitations. A better understanding of the T cell co-signaling pathways would aid investigation of the mechanism, prognosis evaluation, and treatment of AD.

摘要

免疫检查点抑制剂(ICIs)靶向 T 细胞抑制途径的应用彻底改变了癌症治疗。然而,ICIs 可能通过影响 T 细胞的再激活而引发进行性特应性皮炎(AD)。T 细胞在 AD 发病机制中的关键作用是众所周知的。T 细胞共信号通路调节 T 细胞的激活,其中共信号分子对于确定 T 细胞对抗原的反应强度至关重要。鉴于 ICIs 在癌症治疗中的应用日益增加,因此需要及时了解 T 细胞共信号分子在 AD 中的作用。在这篇综述中,我们强调了这些参与 AD 发病机制的分子的重要性。我们还讨论了靶向 T 细胞共信号通路治疗 AD 的潜力,并提出了尚未解决的问题和现有局限性。更好地了解 T 细胞共信号通路将有助于研究 AD 的发病机制、预后评估和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bb/10040887/4b8a1ff9e022/fimmu-14-1081999-g001.jpg

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