Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Research Center for Food Hygiene and Safety, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
BMC Infect Dis. 2024 Oct 16;24(1):1168. doi: 10.1186/s12879-024-10073-0.
Although several genetic biomarkers have been reported in the tocilizumab (TCZ) response in rheumatoid arthritis, no studies have addressed the pharmacogenomics effect of TCZ in COVID-19.
In this prospective longitudinal study, 95 individuals with severe COVID-19 were selected between 2020-2022. The recovery process was measured at 24 h, 48 h, and 10 days before and after taking TCZ. All participants were genotyped using RFLP-PCR. Different genotypes of FCGR2A rs1801274 and IL-6R rs2228145 were compared in terms of the recovery process.
43.2% of patients were male and 56.8% were female with an average age of 58.20(± 16.214) years. The GA genotype for FCGR2A rs1801274 increased the risk of death (OR = 2.83, P = 0.038) and ventilation (OR = 2.71, P = 0.047) in TCZ-treated individuals. However, there was no risk of death and ventilation with IL-6R rs2228145 (P > 0.05). Additionally, docking analysis showed that not only IL6R but also FCGR2A can be a ligand for TCZ.
This study provides valuable insights into the impact of genetic variations on the response rate of TCZ in COVID-19 patients. The GA genotype for FCGR2A rs1801274 was associated with poor treatment outcomes.
尽管已有多项遗传生物标志物被报道与类风湿关节炎中托珠单抗(TCZ)的应答相关,但尚无研究探讨 TCZ 在 COVID-19 中的药物基因组学效应。
在这项前瞻性纵向研究中,于 2020 年至 2022 年期间选择了 95 例重症 COVID-19 患者。在使用 TCZ 前后的 24 小时、48 小时和 10 天分别测量恢复过程。所有参与者均采用 RFLP-PCR 进行基因分型。比较了 FCGR2A rs1801274 和 IL-6R rs2228145 的不同基因型在恢复过程中的差异。
43.2%的患者为男性,56.8%为女性,平均年龄为 58.20(±16.214)岁。FCGR2A rs1801274 的 GA 基因型增加了 TCZ 治疗患者死亡(OR=2.83,P=0.038)和通气(OR=2.71,P=0.047)的风险。然而,IL-6R rs2228145 并没有导致死亡和通气的风险(P>0.05)。此外,对接分析表明,IL6R 以及 FCGR2A 都可以作为 TCZ 的配体。
本研究提供了有价值的见解,了解遗传变异对 COVID-19 患者 TCZ 应答率的影响。FCGR2A rs1801274 的 GA 基因型与较差的治疗结局相关。