Division for Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute 17177 Stockholm, Sweden.
Fraunhofer Institute for Translational Medicine and Pharmacology ITMP 60596 Frankfurt am Main, Germany.
Proc Natl Acad Sci U S A. 2023 Jun 20;120(25):e2218668120. doi: 10.1073/pnas.2218668120. Epub 2023 Jun 12.
A longstanding goal has been to find an antigen-specific preventive therapy, i.e., a vaccine, for autoimmune diseases. It has been difficult to find safe ways to steer the targeting of natural regulatory antigen. Here, we show that the administration of exogenous mouse major histocompatibility complex class II protein bounding a unique galactosylated collagen type II (COL2) peptide (A-galCOL2) directly interacts with the antigen-specific TCR through a positively charged tag. This leads to expanding a VISTA-positive nonconventional regulatory T cells, resulting in a potent dominant suppressive effect and protection against arthritis in mice. The therapeutic effect is dominant and tissue specific as the suppression can be transferred with regulatory T cells, which downregulate various autoimmune arthritis models including antibody-induced arthritis. Thus, the tolerogenic approach described here may be a promising dominant antigen-specific therapy for rheumatoid arthritis, and in principle, for autoimmune diseases in general.
长期以来,人们一直致力于寻找针对自身免疫性疾病的抗原特异性预防疗法,即疫苗。然而,找到安全的方法来引导天然调节性抗原的靶向一直具有挑战性。在这里,我们表明,外源性小鼠主要组织相容性复合体 II 类蛋白结合独特的半乳糖化胶原 II 型 (COL2) 肽 (A-galCOL2) 的给药可通过带正电荷的标签直接与抗原特异性 TCR 相互作用。这导致了 VISTA 阳性非传统调节性 T 细胞的扩增,从而产生强大的显性抑制作用,并防止小鼠发生关节炎。治疗效果具有优势且具有组织特异性,因为抑制作用可以通过调节性 T 细胞转移,调节性 T 细胞可下调包括抗体诱导性关节炎在内的各种自身免疫性关节炎模型。因此,这里描述的耐受方法可能是一种有前途的针对类风湿关节炎的显性抗原特异性治疗方法,原则上也适用于一般的自身免疫性疾病。