Ren Yi, Jahn Denise, Donner Stefanie, Gwinner Clemens, Du Weijie, Wagner Dimitrios L, Tsitsilonis Serafeim, Perka Carsten, Duda Georg, Kienzle Arne
Center for Musculoskeletal Surgery, Clinic for Orthopedics, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Julius Wolff Institute and Center for Musculoskeletal Surgery, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Commun Biol. 2025 May 22;8(1):786. doi: 10.1038/s42003-025-08143-3.
Periprosthetic joint infection (PJI) is a critical complication following arthroplasty, leading to increased prosthesis failure rates post-treatment. This study explores the role of PD-1/PD-L1 signaling in osteoclastogenesis associated with PJI. Peripheral blood, bone, and bone marrow of 65 patients (20 primary osteoarthritis, 21 PJI septic explantation, 24 PJI prosthesis reimplantation) were analyzed for their bone microstructure and cell composition. Immunocytochemistry, RT-qPCR, flow cytometry, bone resorption assay, ELISA, and RNA sequencing were performed to investigate the effects of PD-1 stimulation and blockade on osteoclast formation. PD-1 positive monocytes and sPD-L1 levels were elevated in PJI. Stimulation with PD-L1 enhanced osteoclastogenesis, while PD-1 inhibitor nivolumab reversed these effects. Impact of PD-1 and nivolumab was significantly more pronounced in PJI compared to the control. Our study suggests PD-1/PD-L1 signaling plays a significant role in PJI-related osteoclastogenesis. These findings highlight the potential of PD-1 inhibitors as a novel approach to manage this challenging clinical condition.
人工关节周围感染(PJI)是关节置换术后的一种严重并发症,会导致治疗后假体失败率增加。本研究探讨了PD-1/PD-L1信号通路在与PJI相关的破骨细胞生成中的作用。对65例患者(20例原发性骨关节炎、21例PJI脓毒症切除、24例PJI假体再植入)的外周血、骨骼和骨髓进行了骨微结构和细胞组成分析。采用免疫细胞化学、RT-qPCR、流式细胞术、骨吸收试验、ELISA和RNA测序等方法,研究PD-1刺激和阻断对破骨细胞形成的影响。PJI患者中PD-1阳性单核细胞和sPD-L1水平升高。用PD-L1刺激可增强破骨细胞生成,而PD-1抑制剂纳武单抗可逆转这些作用。与对照组相比,PD-1和纳武单抗在PJI中的影响更为显著。我们的研究表明,PD-1/PD-L1信号通路在PJI相关的破骨细胞生成中起重要作用。这些发现凸显了PD-1抑制剂作为一种治疗这一具有挑战性临床病症的新方法的潜力。