Kalliolias George D, Basdra Efthimia K, Papavassiliou Athanasios G
Hospital for Special Surgery, Arthritis & Tissue Degeneration, New York, NY 10021, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
Biomedicines. 2024 Jan 9;12(1):138. doi: 10.3390/biomedicines12010138.
Evidence from animal models and human genetics implicates Toll-like Receptors (TLRs) in the pathogenesis of Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA). Endosomal TLRs sensing nucleic acids were proposed to induce lupus-promoting signaling in dendritic cells, B cells, monocytes, and macrophages. Ligation of TLR4 in synovial macrophages and fibroblast-like synoviocytes (FLSs) by endogenous ligands was suggested to induce local production of mediators that amplify RA synovitis. Inhibition of TLRs using antagonists or monoclonal antibodies (mAbs) that selectively prevent extracellular or endosomal TLR ligation has emerged as an attractive treatment strategy for SLE and RA. Despite the consistent success of selective inhibition of TLR ligation in animal models, DV-1179 (dual TLR7/9 antagonist) failed to achieve pharmacodynamic effectiveness in SLE, and NI-0101 (mAb against TLR4) failed to improve arthritis in RA. Synergistic cooperation between TLRs and functional redundancy in human diseases may require pharmacologic targeting of intracellular molecules that integrate signaling downstream of multiple TLRs. Small molecules inhibiting shared kinases involved in TLR signaling and peptidomimetics disrupting the assembly of common signalosomes ("Myddosome") are under development. Targeted degraders (proteolysis-targeting chimeras (PROTACs)) of intracellular molecules involved in TLR signaling are a new class of TLR inhibitors with promising preliminary data awaiting further clinical validation.
来自动物模型和人类遗传学的证据表明,Toll样受体(TLRs)与系统性红斑狼疮(SLE)和类风湿性关节炎(RA)的发病机制有关。有人提出,在内体中感知核酸的TLRs可在树突状细胞、B细胞、单核细胞和巨噬细胞中诱导促进狼疮的信号传导。内源性配体与滑膜巨噬细胞和成纤维细胞样滑膜细胞(FLS)中的TLR4结合,被认为可诱导介质的局部产生,从而放大RA滑膜炎。使用拮抗剂或单克隆抗体(mAb)抑制TLRs,选择性地阻止细胞外或内体TLR结合,已成为治疗SLE和RA的一种有吸引力的策略。尽管在动物模型中选择性抑制TLR结合取得了持续成功,但DV-1179(双重TLR7/9拮抗剂)在SLE中未能实现药效学有效性,而NI-0101(抗TLR4单克隆抗体)未能改善RA中的关节炎。TLRs之间的协同合作以及人类疾病中的功能冗余可能需要对整合多个TLRs下游信号的细胞内分子进行药理学靶向。正在开发抑制TLR信号传导中涉及的共享激酶的小分子和破坏常见信号小体(“Myddosome”)组装的拟肽。参与TLR信号传导的细胞内分子的靶向降解剂(蛋白酶靶向嵌合体(PROTACs))是一类新型的TLR抑制剂,有前景的初步数据有待进一步临床验证。