CNRS UMR 5234, Fundamental Microbiology and Pathogenicity, University Bordeaux, Bordeaux, France.
MAS Yolaine-de-Kepper, Saint-Georges-sur-Loire, France.
Rev Neurol (Paris). 2023 Nov;179(9):983-992. doi: 10.1016/j.neurol.2023.04.003. Epub 2023 Aug 24.
Patients with severe neuromuscular disease (sNMD) are considered at high risk of severe COVID-19. Muscle tissue is often replaced by fibroadipose tissue in these diseases whereas the new mRNA-based vaccines are injected intramuscularly. We aimed at evaluating the efficacy of two injections associated with a booster injection of mRNA vaccine in these patients.
We performed an observational, prospective, single-centre study to investigate the level of anti-S antibodies (Abs) and their neutralization activity at weeks 6 (W6) and 24 (W24) after two injections of mRNA-1273 vaccine and at weeks 12 (BW12) and 29 (BW29) after a booster injection of BNT162b2 vaccine in patients with sNMD.
Thirty-three patients with sNMD were included. At W6, 30 patients (90.1%) showed a protective serum level of specific anti-S Abs with a strong neutralization capacity. We observed a decline over time: only 12 patients (36.3%) retained anti-S Abs levels considered as protective at W24. The neutralization activity remained above the cut off in 23 (69.7%). The booster vaccination restored robust neutralization activity for all analysed 22 patients (100%) at BW12, which was maintained without any significant drop at BW29 (16). No severe adverse event was reported in this cohort and none of the 33 patients developed symptomatic COVID-19 over one year.
This study provides evidence that most sNMD patients receiving two injections of COVID-19 mRNA-based vaccines develop a strong humoral response after vaccination. A decline over time was observed but a single booster injection restores a long-term immunity. Moreover, no safety issues were observed.
患有严重神经肌肉疾病(sNMD)的患者被认为有发生严重 COVID-19 的高风险。这些疾病中,肌肉组织常被纤维脂肪组织取代,而新的基于 mRNA 的疫苗是肌肉内注射的。我们旨在评估这些患者接种两剂疫苗和一剂加强针的 mRNA 疫苗的效果。
我们进行了一项观察性、前瞻性、单中心研究,以调查 33 例 sNMD 患者在接种两剂 mRNA-1273 疫苗后 6 周(W6)和 24 周(W24)以及接种一剂 BNT162b2 疫苗加强针后 12 周(BW12)和 29 周(BW29)时抗-S 抗体(Abs)的水平及其中和活性。
33 例 sNMD 患者入组。在 W6 时,30 例患者(90.1%)表现出保护性血清水平的特异性抗-S Abs,具有较强的中和能力。我们观察到随着时间的推移而下降:只有 12 例患者(36.3%)在 W24 时保留了被认为具有保护作用的抗-S Abs 水平。中和活性在 23 例患者(69.7%)中仍高于截止值。加强接种在所有分析的 22 例患者(100%)中恢复了强大的中和活性,在 BW29 时没有任何显著下降(16 例)。该队列中未报告严重不良事件,33 例患者在一年中均未发生有症状的 COVID-19。
这项研究提供了证据表明,大多数接受两剂 COVID-19 基于 mRNA 的疫苗接种的 sNMD 患者在接种后会产生强烈的体液免疫反应。随着时间的推移观察到下降,但单次加强接种可恢复长期免疫。此外,未观察到安全性问题。