Schall Nicolas, Talamini Laura, Wilhelm Maud, Jouvin-Marche Evelyne, Muller Sylviane
CNRS and Strasbourg University, Unit Biotechnology and Cell signaling, UMR7242/Strasbourg Drug Discovery and Development Institute (IMS), Strasbourg, France.
Institute for Advanced Biosciences, Research Centre Université Grenoble Alpes (UGA)-Inserm U1209-CNRS UMR 5309, La Tronche, France.
Front Immunol. 2022 Jun 1;13:904669. doi: 10.3389/fimmu.2022.904669. eCollection 2022.
In systemic lupus erythematosus, T cells display multiple abnormalities. They are abnormally activated, secrete pro-inflammatory cytokines, help B cells to generate pathogenic autoantibodies, and provoke the accumulation of autoreactive memory T cells. P140, a synthetic peptide evaluated in phase-III clinical trials for lupus, binds HSPA8/HSC70 chaperone protein. and , it interferes with hyperactivated chaperone-mediated autophagy, modifying overexpression of major histocompatibility complex class II molecules and antigen presentation to autoreactive T cells. Here, we show that in P140-treated lupus mice, abnormalities affecting T and B cells are no longer detectable in secondary lymphoid tissue and peripheral blood. Data indicate that P140 acts by depleting hyper-activated autoreactive T and B cells and restores normal immune homeostasis. Our findings suggest that P140 belongs to a new family of non-immunosuppressive immunoregulators that do not correct T and B cell abnormalities but rather contribute to the clearance of deleterious T and B cells.
在系统性红斑狼疮中,T细胞表现出多种异常。它们被异常激活,分泌促炎细胞因子,帮助B细胞产生致病性自身抗体,并促使自身反应性记忆T细胞积累。P140是一种在狼疮的III期临床试验中评估的合成肽,它与HSPA8/HSC70伴侣蛋白结合。此外,它干扰过度激活的伴侣介导的自噬,改变主要组织相容性复合体II类分子的过表达以及向自身反应性T细胞的抗原呈递。在这里,我们表明,在P140治疗的狼疮小鼠中,影响T细胞和B细胞的异常在次级淋巴组织和外周血中不再可检测到。数据表明,P140通过消耗过度激活的自身反应性T细胞和B细胞起作用,并恢复正常的免疫稳态。我们的研究结果表明,P140属于一类新的非免疫抑制性免疫调节剂,它们不是纠正T细胞和B细胞异常,而是有助于清除有害的T细胞和B细胞。