Dequidt Tanguy, Richier Quentin, Louapre Céline, Ader Florence, Merad Yanis, Lauwerier Nicolas, Jacomet Christine, Carles Michel, Biron Charlotte, Gendrin Vincent, Marlat Clément, Danion François, Lepage Tristan M, Sotto Albert, Bourdellon Loïc, Mania Alexandre, Martinot Martin, Falher Georges Le, Ferre Alexis, Pilmis Benoit, Gondran Guillaume, Simeone Pierre, Henry Matthieu, Kamel Toufik, Ray Simon, Ancellin Sophie, Mélé Nicolas, Camou Fabrice, Destremau Marjolaine, Sellenet Jeremy, Zucman Noémie, Le Maréchal Marion, Mellouki Khawla, Langlois Marie-Elodie, Luque Paz David, Mousset Maud, Leclerc Catherine, Sommet Agnès, Lacombe Karine, Martin-Blondel Guillaume
Department of Infectious Diseases, Guadeloupe University hospital, Pointe-à-Pitre, France.
Sorbonne University, Department of Infectious Diseases, Saint Antoine Hospital, APHP, Paris, France.
Int J Infect Dis. 2025 Feb;151:107323. doi: 10.1016/j.ijid.2024.107323. Epub 2024 Dec 4.
Despite vaccination, patients receiving anti-CD20 monoclonal antibodies (mAbs) for multiple sclerosis (MS) or neuromyelitis optica spectrum disorders (NMOSD) have an increased risk of developing severe or protracted COVID-19. The aim of this study was to describe the effect of COVID-19 convalescent plasma (CCP) in patients with MS or NMOSD exposed to anti-CD20 and infected by SARS-CoV-2.
This French national, retrospective cohort study was conducted between November 2020 and June 2023. Patients with MS or NMOSD, under anti-CD20 mAbs, with symptomatic COVID-19 and treated by CCP were screened. Protracted COVID-19 was defined by a duration of symptoms >21 days. The primary endpoint was the overall survival 30 days after CCP administration.
Ninety-two patients from 34 hospitals were included, 84 (91%) with MS and 8 (9%) with NMOSD. Overall, 30-day survival was 97% (IC95%: 91-99). SARS-CoV-2 viremia was positive in 47/75 (61%) patients before CCP versus 9/59 (15%) seven days post-CCP. In the 52 patients (57%) with protracted COVID-19, the duration of symptoms before CCP was 51 [28-69] days, including fever in 75% of cases, which disappeared in 100% of patients 7 days post-CCP.
CCP could be a therapeutic option in patients exposed to anti-CD20 mAbs for inflammatory demyelinating disease, particularly in those with protracted COVID-19.
尽管接种了疫苗,但接受抗CD20单克隆抗体(mAb)治疗的多发性硬化症(MS)或视神经脊髓炎谱系障碍(NMOSD)患者发生重症或持续性新型冠状病毒肺炎(COVID-19)的风险增加。本研究的目的是描述COVID-19康复期血浆(CCP)对接受抗CD20治疗且感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的MS或NMOSD患者的影响。
这项法国全国性的回顾性队列研究于2020年11月至2023年6月进行。筛选接受抗CD20 mAb治疗、出现症状性COVID-19并接受CCP治疗的MS或NMOSD患者。持续性COVID-19定义为症状持续时间>21天。主要终点是CCP给药后30天的总生存率。
纳入了来自34家医院的92例患者,其中84例(91%)患有MS,8例(9%)患有NMOSD。总体而言,30天生存率为97%(95%置信区间:91%-99%)。CCP治疗前,47/75(61%)的患者严重急性呼吸综合征冠状病毒2病毒血症呈阳性,而CCP治疗7天后,这一比例为9/59(15%)。在52例(57%)持续性COVID-19患者中,CCP治疗前症状持续时间为51[28-69]天,75%的病例有发热症状,CCP治疗7天后100%的患者发热症状消失。
CCP可能是炎性脱髓鞘疾病接受抗CD20 mAb治疗患者的一种治疗选择,特别是对于持续性COVID-19患者。