Jaber Aliya, Patel Meera, Sylvester Andrew, Yarussi Mary, Kalina J Tamar, Mendoza Jason P, Avila Robin L, Tremblay Matthew A
Multiple Sclerosis Comprehensive Care Center, RWJ Barnabas Health, Livingston, NJ, USA.
Biogen, Weston, MA, USA.
Neurol Ther. 2023 Apr;12(2):687-700. doi: 10.1007/s40120-023-00448-x. Epub 2023 Feb 16.
Some multiple sclerosis (MS) disease-modifying therapies (DMTs) impair responses to vaccines, emphasizing the importance of understanding COVID-19 vaccine immune responses in people with MS (PwMS) receiving different DMTs.
This prospective, open-label observational study enrolled 45 participants treated with natalizumab (n = 12), ocrelizumab (n = 16), fumarates (dimethyl fumarate or diroximel fumarate, n = 11), or interferon beta (n = 6); ages 18-65 years inclusive; stable on DMT for at least 6 months. Responder rates, anti-SARS-CoV-2 spike receptor-binding domain IgG (anti-RBD) geometric mean titers (GMTs), antigen-specific T cells, and vaccination-related adverse events were evaluated at baseline and 8, 24, 36, and 48 weeks after first mRNA-1273 (Moderna) dose.
At 8 weeks post vaccination, all natalizumab-, fumarate-, and interferon beta-treated participants generated detectable anti-RBD IgG titers, compared to only 25% of the ocrelizumab cohort. At 24 and 36 weeks post vaccination, natalizumab-, fumarate-, and interferon beta-treated participants continued to demonstrate detectable anti-RBD IgG titers, whereas participants receiving ocrelizumab did not. Anti-RBD GMTs decreased 81.5% between 8 and 24 weeks post vaccination for the non-ocrelizumab-treated participants, with no significant difference between groups. At 36 weeks post vaccination, ocrelizumab-treated participants had higher proportions of spike-specific T cells compared to other treatment groups. Vaccine-associated side effects were highest in the ocrelizumab arm for most symptoms.
These results suggest that humoral response to mRNA-1273 COVID-19 vaccine is preserved and similar in PwMS treated with natalizumab, fumarate, and interferon beta, but muted with ocrelizumab. All DMTs had preserved T cell response, including the ocrelizumab cohort, which also had a greater risk of vaccine-related side effects.
一些多发性硬化症(MS)疾病修正疗法(DMTs)会损害对疫苗的反应,这凸显了了解接受不同DMTs治疗的多发性硬化症患者(PwMS)对新冠疫苗免疫反应的重要性。
这项前瞻性、开放标签观察性研究纳入了45名参与者,他们分别接受那他珠单抗(n = 12)、奥瑞珠单抗(n = 16)、富马酸盐(富马酸二甲酯或二甲基富马酸罗昔麦尔,n = 11)或干扰素β(n = 6)治疗;年龄在18至65岁之间;DMT治疗稳定至少6个月。在基线以及首次接种mRNA-1273(Moderna)疫苗后第8、24、36和48周评估应答率、抗SARS-CoV-2刺突受体结合域IgG(抗RBD)几何平均滴度(GMTs)、抗原特异性T细胞以及与疫苗接种相关的不良事件。
接种疫苗后8周,所有接受那他珠单抗、富马酸盐和干扰素β治疗的参与者均产生了可检测到的抗RBD IgG滴度,而奥瑞珠单抗组只有25%的参与者产生了该滴度。接种疫苗后24周和36周,接受那他珠单抗、富马酸盐和干扰素β治疗的参与者继续表现出可检测到的抗RBD IgG滴度,而接受奥瑞珠单抗治疗的参与者则没有。对于未接受奥瑞珠单抗治疗的参与者,接种疫苗后8至24周抗RBD GMTs下降了81.5%,各治疗组之间无显著差异。接种疫苗后36周,与其他治疗组相比,接受奥瑞珠单抗治疗的参与者中刺突特异性T细胞比例更高。对于大多数症状,奥瑞珠单抗组的疫苗相关副作用最高。
这些结果表明,接受那他珠单抗、富马酸盐和干扰素β治疗的PwMS对mRNA-1273新冠疫苗的体液反应得以保留且相似,但接受奥瑞珠单抗治疗的患者反应较弱。所有DMTs均保留了T细胞反应,包括奥瑞珠单抗组,该组也有更高的疫苗相关副作用风险。