Moderna, Inc., Cambridge, MA, USA.
Massachusetts General Hospital, Boston, MA, USA.
Nat Med. 2021 Dec;27(12):2224-2233. doi: 10.1038/s41591-021-01573-6. Epub 2021 Dec 9.
Chikungunya virus (CHIKV) infection causes acute disease characterized by fever, rash and arthralgia, which progresses to severe and chronic arthritis in up to 50% of patients. Moreover, CHIKV infection can be fatal in infants or immunocompromised individuals and has no approved therapy or prevention. This phase 1, first-in-human, randomized, placebo-controlled, proof-of-concept trial conducted from January 2019 to June 2020 evaluated the safety and pharmacology of mRNA-1944, a lipid nanoparticle-encapsulated messenger RNA encoding the heavy and light chains of a CHIKV-specific monoclonal neutralizing antibody, CHKV-24 ( NCT03829384 ). The primary outcome was to evaluate the safety and tolerability of escalating doses of mRNA-1944 administered via intravenous infusion in healthy participants aged 18-50 years. The secondary objectives included determination of the pharmacokinetics of mRNA encoding for CHKV-24 immunoglobulin heavy and light chains and ionizable amino lipid component and the pharmacodynamics of mRNA-1944 as assessed by serum concentrations of mRNA encoding for CHKV-24 immunoglobulin G (IgG), plasma concentrations of ionizable amino lipid and serum concentrations of CHKV-24 IgG. Here we report the results of a prespecified interim analysis of 38 healthy participants who received intravenous single doses of mRNA-1944 or placebo at 0.1, 0.3 and 0.6 mg kg, or two weekly doses at 0.3 mg kg. At 12, 24 and 48 h after single infusions, dose-dependent levels of CHKV-24 IgG with neutralizing activity were observed at titers predicted to be therapeutically relevant concentrations (≥1 µg ml) across doses that persisted for ≥16 weeks at 0.3 and 0.6 mg kg (mean t approximately 69 d). A second 0.3 mg kg dose 1 week after the first increased CHKV-24 IgG levels 1.8-fold. Adverse effects were mild to moderate in severity, did not worsen with a second mRNA-1944 dose and none were serious. To our knowledge, mRNA-1944 is the first mRNA-encoded monoclonal antibody showing in vivo expression and detectable ex vivo neutralizing activity in a clinical trial and may offer a treatment option for CHIKV infection. Further evaluation of the potential therapeutic use of mRNA-1944 in clinical trials for the treatment of CHIKV infection is warranted.
基孔肯雅病毒(CHIKV)感染会引起急性疾病,其特征为发热、皮疹和关节炎,多达 50%的患者会发展为严重和慢性关节炎。此外,CHIKV 感染在婴儿或免疫功能低下的个体中可能是致命的,并且目前尚无批准的治疗或预防方法。这项从 2019 年 1 月至 2020 年 6 月进行的、1 期、首次人体、随机、安慰剂对照、概念验证试验,评估了脂质纳米颗粒包裹的编码 CHIKV 特异性单克隆中和抗体 CHKV-24 的重链和轻链的信使 RNA(mRNA-1944)的安全性和药理学,该抗体由信使 RNA 编码(NCT03829384)。主要结局是评估健康参与者(18-50 岁)静脉输注递增剂量的 mRNA-1944 的安全性和耐受性。次要目标包括确定编码 CHKV-24 免疫球蛋白重链和轻链以及可离子化氨基酸脂质成分的 mRNA 的药代动力学,以及通过血清中编码 CHKV-24 免疫球蛋白 G(IgG)的 mRNA 浓度、血浆中可离子化氨基酸脂质浓度和血清中 CHKV-24 IgG 浓度评估 mRNA-1944 的药效动力学。在这里,我们报告了对 38 名健康参与者的预先指定的中期分析结果,这些参与者在 0.1、0.3 和 0.6mg/kg 时接受了静脉单次剂量的 mRNA-1944 或安慰剂,或在 0.3mg/kg 时接受了两次每周剂量。在单次输注后 12、24 和 48 小时,观察到具有中和活性的 CHKV-24 IgG 的剂量依赖性水平,在预测有治疗意义的浓度(≥1μg/ml)时,在 0.3 和 0.6mg/kg 剂量下的效价持续至少 16 周(平均 t 约为 69 天)。第一次输注后一周给予第二次 0.3mg/kg 剂量可使 CHKV-24 IgG 水平增加 1.8 倍。不良反应的严重程度为轻度至中度,第二次接受 mRNA-1944 后不会加重,且均不严重。据我们所知,mRNA-1944 是第一个在临床试验中体内表达并可检测到体外中和活性的 mRNA 编码单克隆抗体,可能为 CHIKV 感染提供一种治疗选择。有必要进一步评估在临床试验中使用 mRNA-1944 治疗 CHIKV 感染的潜在治疗用途。