Mathew Thomas, Garg Surabhi, John Saji K, Kimi Mal S, Chhakchhuak Naom Z, Koshy Sherina, Yangdonq Tenzin, George Molly, Bhardwaj Shagun, Reddy Yerasu M, Murgod Uday, Kamath Vikram, Shivde Sonia, Badachi Sagar, Huddar Akshata, Sarma Gosala R K, Nadig Raghunandan
Department of Neurology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.
Department of Neurology, Care Hospital, Hyderabad, Telangana, India.
Ann Indian Acad Neurol. 2024 May 1;27(3):264-268. doi: 10.4103/aian.aian_151_24. Epub 2024 Jun 20.
The impact of coronavirus disease 2019 (COVID-19) infection on patients with multiple sclerosis (MS) undergoing various immunomodulating therapies can vary. Individuals on B-cell therapy, such as rituximab, may be more susceptible to infection compared to those treated with natalizumab.
The objective of this study was to determine the incidence and severity of COVID-19 infection in patients receiving rituximab, natalizumab, and healthy controls.
This retrospective multicentric study included data derived from a centralized MS registry of four centers in South India. Data of patients on rituximab and natalizumab recruited between 2020 February and 2022 December were extracted from the registry and analyzed. The outcomes studied were the occurrence of COVID-19 infection, hospitalization, intensive care unit admission, death, post-COVID-19 relapses, and post-vaccine relapses. These outcomes were compared between the treatment groups and the matched controls.
COVID-19 infection occurred in 49.1% (26/53) of those on rituximab, 19.2% (5/26) of those on natalizumab, and 11.5% (6/52) of healthy controls. In addition, 8/53 (15.1%) in the rituximab group and 1/26 (3.8%) in the natalizumab group were hospitalized. All 6/52 (11.5%) in the control group had mild infection, and none were hospitalized. No deaths occurred in any group. On statistical analysis, the occurrence of COVID-19 infection in the rituximab group was significantly higher when compared to natalizumab ( P = 0.0141) and healthy controls ( P < 0.001). Hospitalizations were significantly higher in the rituximab group when compared to healthy controls ( P < 0.006).
MS patients treated with rituximab were more likely to experience COVID-19 infection compared to those treated with natalizumab and healthy controls. Hospitalization was more frequently seen in patients treated with rituximab compared to healthy controls.
2019年冠状病毒病(COVID-19)感染对接受各种免疫调节治疗的多发性硬化症(MS)患者的影响可能有所不同。与接受那他珠单抗治疗的患者相比,接受B细胞疗法(如利妥昔单抗)的个体可能更容易感染。
本研究的目的是确定接受利妥昔单抗、那他珠单抗治疗的患者以及健康对照中COVID-19感染的发生率和严重程度。
这项回顾性多中心研究纳入了来自印度南部四个中心的集中式MS登记处的数据。从登记处提取并分析了2020年2月至2022年12月期间招募的接受利妥昔单抗和那他珠单抗治疗的患者的数据。研究的结局包括COVID-19感染的发生、住院、重症监护病房入院、死亡、COVID-19后复发以及疫苗接种后复发。对治疗组和匹配的对照组的这些结局进行了比较。
接受利妥昔单抗治疗的患者中49.1%(26/53)发生了COVID-19感染,接受那他珠单抗治疗的患者中19.2%(5/26)发生了感染,健康对照中11.5%(6/52)发生了感染。此外,利妥昔单抗组中有8/53(15.1%)住院,那他珠单抗组中有1/26(3.8%)住院。对照组中所有6/52(11.5%)均为轻度感染,无人住院。任何组均未发生死亡。经统计学分析,与那他珠单抗组(P = 0.0141)和健康对照组(P < 0.001)相比,利妥昔单抗组中COVID-19感染的发生率显著更高。与健康对照组相比,利妥昔单抗组的住院率显著更高(P < 0.006)。
与接受那他珠单抗治疗的患者和健康对照相比,接受利妥昔单抗治疗的MS患者更有可能发生COVID-19感染。与健康对照相比,接受利妥昔单抗治疗的患者住院更为常见。