Department of Immunology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Neurology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Iran J Immunol. 2023 Mar 14;20(1):104-113. doi: 10.22034/iji.2023.96695.2453.
Abnormal humoral and cellular immune responses have been reported in immune-mediated polyneuropathies. CD137, as a costimulatory molecule and a TNF receptor superfamily member, has been demonstrated to have a key role in the pathogenesis of many autoimmune as well as inflammatory disorders.
To evaluate the transcripts levels of CD137, its ligand (CD137L), and the serum levels of soluble CD137 (sCD137) in patients with immune-mediated polyneuropathy.
A total of 45 patients and 46 sex and age-matched healthy individuals were enrolled in the study. CD137 and CD137L transcript levels were assessed by the Real-Time PCR, and the serum level of sCD137 was measured using the ELISA technique. The Bayesian regression model was used for statistical analysis at the 0.05 significance level in R 4.1.0 statistical environment.
Transcript levels of the CD137 and CD137L were higher in polyneuropathy patients in comparison with the healthy subjects (P=0.006 for both). Conversely, the mean level of sCD137 was significantly lower in the sera of patients compared to the controls (P<0.001).
Our findings point to the possible role of CD137 and CD137L in immune-mediated polyneuropathy pathogenesis. More investigations are required to clarify the exact contributions of the mentioned molecules to the pathogenesis of immune-mediated polyneuropathies.
体液和细胞免疫应答异常已在免疫介导性多发性神经病中报道。CD137 作为一种共刺激分子和 TNF 受体超家族成员,已被证明在许多自身免疫和炎症性疾病的发病机制中具有关键作用。
评估免疫介导性多发性神经病患者中 CD137、其配体(CD137L)的转录水平和可溶性 CD137(sCD137)的血清水平。
共纳入 45 例患者和 46 名性别和年龄匹配的健康个体。采用实时 PCR 评估 CD137 和 CD137L 的转录水平,采用 ELISA 技术测量 sCD137 的血清水平。在 R 4.1.0 统计环境中,采用贝叶斯回归模型进行统计分析,置信水平为 0.05。
与健康对照组相比,多发性神经病患者的 CD137 和 CD137L 转录水平更高(均 P=0.006)。相反,与对照组相比,患者血清中 sCD137 的平均水平显著降低(P<0.001)。
我们的发现表明 CD137 和 CD137L 可能在免疫介导性多发性神经病的发病机制中起作用。需要进一步研究来阐明这些分子对免疫介导性多发性神经病发病机制的确切贡献。