Michiels Yves, Houhou-Fidouh Nadhira, Collin Gilles, Berger Jérôme, Kohli Evelyne
Community Pharmacy, Center for Primary Care and Public Health (Unisanté) Lausanne 1011, University of Lausanne, 1015 Lausanne, Switzerland.
Pharmacie Michiels, Research Department, 21600 Longvic, France.
Vaccines (Basel). 2021 Oct 6;9(10):1140. doi: 10.3390/vaccines9101140.
Patients with multiple sclerosis (MS) are treated with drugs that may impact immune responses to SARS-CoV-2 vaccination. Evaluation of "prime-boost" (heterologous) vaccination regimens including a first administration of a viral vector-based vaccine and a second one of an mRNA-based vaccine in such patients has not yet been completed. Here, we present the anti-spike protein S humoral response, including the neutralizing antibody response, in a 54-year-old MS patient who had been treated with teriflunomide for the past 2 years and who received a heterologous ChAdOx1 nCoV-19/ BNT162b2 vaccination regimen. The results showed a very strong anti-S IgG response and a good neutralizing antibody response. These results show that teriflunomide did not prevent the development of a satisfactory humoral response in this MS patient after vaccination with a ChAdOx1 nCoV-19/ BNT162b2 prime-boost protocol.
患有多发性硬化症(MS)的患者会接受可能影响对SARS-CoV-2疫苗免疫反应的药物治疗。对包括首次接种基于病毒载体的疫苗和第二次接种基于mRNA的疫苗的“初免-加强”(异源)疫苗接种方案在这类患者中的评估尚未完成。在此,我们展示了一名54岁MS患者的抗刺突蛋白S体液反应,包括中和抗体反应,该患者在过去2年中接受了特立氟胺治疗,并接受了异源ChAdOx1 nCoV-19/BNT162b2疫苗接种方案。结果显示出非常强烈的抗S IgG反应和良好的中和抗体反应。这些结果表明,在采用ChAdOx1 nCoV-19/BNT162b2初免-加强方案接种疫苗后,特立氟胺并未阻止该MS患者产生令人满意的体液反应。