From the Division of Multiple Sclerosis (S.T., S.G., C.L., E.J.K., C.P., L.Z., L.D.Y., M.K.S., J.R.B., C.M., A.B.-O., R.F., R.B., A.A.P., D.A.J.), Hospital of the University of Pennsylvania and Perelman School of Medicine; Division of Infectious Diseases (C.C.), Department of Medicine; and Weill Institute for Neurosciences (M.R.W.), Department of Neurology, University of California, San Francisco.
Neurol Neuroimmunol Neuroinflamm. 2023 Aug 10;10(5). doi: 10.1212/NXI.0000000000200154. Print 2023 Sep.
The objective of this study was to report on the development of neuroinvasive West Nile virus (WNV) infection in the context of anti-CD20 monotherapy for multiple sclerosis (MS).
This is a case series study.
In 2021-2022, we observed 4 cases of neuroinvasive WNV infection in our patient population of 2009 patients with MS on ocrelizumab, compared with a total of 46 cases of neuroinvasive WNV infection reported in Pennsylvania and 40 in New Jersey. Odds were 258 times that of the general population (95% confidence interval 97-691), χ < 0.0001). All were women aged 41-61 years with variable disease duration, level of disability, and duration of anti-CD20 therapy. All presented in summer/early fall with fever, headache, and encephalopathy consistent with meningoencephalitis. Three patients had acute cerebellitis. Two had anterior nerve root involvement progressing to quadriparesis, and 1 developed refractory nonconvulsive status epilepticus. All required intubation and experienced significant morbidity. All had CSF pleocytosis. Two patients were WNV IgM positive in both the serum and CSF, 1 patient had positive serum IgM and CSF metagenomic next-generation sequencing (mNGS), while 1 had positive CSF mNGS with negative serum and CSF antibodies.
Neuroinvasive WNV infection can develop with anti-CD20 monotherapy in the absence of additional immunosuppression. WNV serologies may be negative in the setting of anti-CD20 treatment; in the appropriate clinical context, one should consider direct detection methods such as PCR or mNGS-based testing.
本研究旨在报告在多发性硬化症(MS)患者接受抗 CD20 单药治疗的背景下,发生神经侵袭性西尼罗河病毒(WNV)感染的情况。
这是一项病例系列研究。
在 2021-2022 年,我们在接受奥瑞珠单抗治疗的 2009 例 MS 患者中观察到 4 例神经侵袭性 WNV 感染病例,而宾夕法尼亚州共报告了 46 例神经侵袭性 WNV 感染病例,新泽西州报告了 40 例。感染风险是普通人群的 258 倍(95%置信区间 97-691),χ < 0.0001)。所有患者均为 41-61 岁女性,疾病持续时间、残疾程度和抗 CD20 治疗时间不同。所有患者均在夏季/初秋出现发热、头痛和脑炎,符合脑膜脑炎表现。3 例患者出现急性小脑炎。2 例患者出现前神经根受累,进展为四肢瘫痪,1 例患者出现难治性非惊厥性癫痫持续状态。所有患者均需要插管,且均出现严重并发症。所有患者的脑脊液均出现白细胞增多。2 例患者的血清和脑脊液均WNV IgM 阳性,1 例患者的血清 IgM 和脑脊液宏基因组下一代测序(mNGS)阳性,1 例患者的脑脊液 mNGS 阳性,而血清和脑脊液抗体均为阴性。
在没有额外免疫抑制的情况下,抗 CD20 单药治疗也可能导致神经侵袭性 WNV 感染。在抗 CD20 治疗的背景下,WNV 血清学可能为阴性;在适当的临床情况下,应考虑直接检测方法,如 PCR 或基于 mNGS 的检测。