Drake University College of Pharmacy and Health Sciences, Des Moines, IA, USA.
Am J Health Syst Pharm. 2022 Nov 22;79(23):2099-2117. doi: 10.1093/ajhp/zxac244.
Type 1 diabetes (T1D) is an autoimmune disease characterized by the destruction of beta cells, resulting in a loss of insulin production. Patients with T1D carry a substantial disease burden as well as substantial short-term and long-term risks associated with inadequate glycemic control. Currently, treatment mainly consists of insulin, which only treats the symptoms of T1D and not the root cause. Thus, disease-modifying agents such as anti-CD3 monoclonal antibodies (mAbs) that target the autoimmune destruction of beta cells in T1D would provide significant relief and health benefits for patients with T1D. This review summarizes the clinical evidence regarding the safety and efficacy of anti-CD3 mAbs in the prevention and treatment of T1D.
A total of 27 studies reporting or evaluating data from clinical trials involving otelixizumab and teplizumab were included in the review. Anti-CD3 mAbs have shown significant benefits in both patients at high risk for T1D and those with recent-onset T1D. In high-risk populations, anti-CD3 mAbs delayed time to diagnosis, preserved C-peptide levels, and improved metabolic parameters. In recent-onset T1D, anti-CD3 mAbs preserved C-peptide levels and reduced insulin needs for extended periods. Anti-CD3 mAb therapy appears to be safe, with primarily transient and self-limiting adverse effects and no negative long-term effects.
Anti-CD3 mAbs are promising disease-modifying treatments for T1D. Their role in T1D may introduce short-term and long-term benefits with the potential to mitigate the significant disease burden; however, more evidence is required for an accurate assessment.
1 型糖尿病(T1D)是一种自身免疫性疾病,其特征是β细胞的破坏,导致胰岛素产生丧失。T1D 患者不仅承担着巨大的疾病负担,还面临着因血糖控制不佳而导致的大量短期和长期风险。目前,治疗主要依赖胰岛素,只能缓解 T1D 的症状,而不能根治其根本病因。因此,抗 CD3 单克隆抗体(mAb)等能够针对 T1D 中β细胞的自身免疫破坏的疾病修饰药物,将为 T1D 患者带来显著的缓解和健康获益。本综述总结了抗 CD3 mAb 用于预防和治疗 T1D 的安全性和疗效的临床证据。
本综述共纳入了 27 项研究,这些研究报告了或评估了包含 otelixizumab 和 teplizumab 的临床试验数据。抗 CD3 mAb 在 T1D 高危人群和近期发病的 T1D 患者中均显示出显著获益。在高危人群中,抗 CD3 mAb 可延迟 T1D 诊断时间、保持 C 肽水平,并改善代谢参数。在近期发病的 T1D 患者中,抗 CD3 mAb 可延长 C 肽水平保留时间,并减少胰岛素需求。抗 CD3 mAb 治疗似乎是安全的,主要表现为短暂且自限性的不良反应,且无长期负面影响。
抗 CD3 mAb 是治疗 T1D 的有前途的疾病修饰疗法。它们在 T1D 中的作用可能会带来短期和长期的获益,有潜力减轻巨大的疾病负担;但需要更多的证据进行准确评估。