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急性弛缓性脊髓炎患者脑脊液中肠道病毒抗体。

Antibodies to Enteroviruses in Cerebrospinal Fluid of Patients with Acute Flaccid Myelitis.

机构信息

Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, New York, USA.

Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

mBio. 2019 Aug 13;10(4):e01903-19. doi: 10.1128/mBio.01903-19.

Abstract

Acute flaccid myelitis (AFM) has caused motor paralysis in >560 children in the United States since 2014. The temporal association of enterovirus (EV) outbreaks with increases in AFM cases and reports of fever, respiratory, or gastrointestinal illness prior to AFM in >90% of cases suggest a role for infectious agents. Cerebrospinal fluid (CSF) from 14 AFM and 5 non-AFM patients with central nervous system (CNS) diseases in 2018 were investigated by viral-capture high-throughput sequencing (VirCapSeq-VERT system). These CSF and serum samples, as well as multiple controls, were tested for antibodies to human EVs using peptide microarrays. EV RNA was confirmed in CSF from only 1 adult AFM case and 1 non-AFM case. In contrast, antibodies to EV peptides were present in CSF of 11 of 14 AFM patients (79%), significantly higher than controls, including non-AFM patients (1/5 [20%]), children with Kawasaki disease (0/10), and adults with non-AFM CNS diseases (2/11 [18%]) ( = 0.023, 0.0001, and 0.0028, respectively). Six of 14 CSF samples (43%) and 8 of 11 sera (73%) from AFM patients were immunoreactive to an EV-D68-specific peptide, whereas the three control groups were not immunoreactive in either CSF (0/5, 0/10, and 0/11; = 0.008, 0.0003, and 0.035, respectively) or sera (0/2, 0/8, and 0/5; = 0.139, 0.002, and 0.009, respectively). The presence in cerebrospinal fluid of antibodies to EV peptides at higher levels than non-AFM controls supports the plausibility of a link between EV infection and AFM that warrants further investigation and has the potential to lead to strategies for diagnosis and prevention of disease.

摘要

自 2014 年以来,急性弛缓性脊髓炎(AFM)在美国已导致 560 多名儿童出现运动麻痹。肠病毒(EV)爆发与 AFM 病例增加之间的时间关联,以及在 90%以上的病例中出现发热、呼吸道或胃肠道疾病之前有 AFM 报告,提示存在传染性病原体。对 2018 年 14 例 AFM 和 5 例中枢神经系统(CNS)疾病非 AFM 患者的脑脊液(CSF)进行了病毒捕获高通量测序(VirCapSeq-VERT 系统)研究。使用肽微阵列对这些 CSF 和血清样本以及多个对照样本进行了针对人类 EV 的抗体检测。仅在 1 例成人 AFM 病例和 1 例非 AFM 病例的 CSF 中确认存在 EV RNA。相比之下,14 例 AFM 患者中有 11 例(79%)的 CSF 中存在针对 EV 肽的抗体,明显高于对照组,包括非 AFM 患者(5 例中的 1 例[20%])、川崎病患儿(10 例中的 0 例)和非 AFM CNS 疾病成人(11 例中的 2 例[18%])(=0.023,0.0001,0.0028)。14 例 CSF 样本中的 6 例(43%)和 11 例血清样本中的 8 例(73%)来自 AFM 患者,对 EV-D68 特异性肽呈免疫反应性,而三个对照组在 CSF(5 例中均无,10 例中均无,11 例中均无;=0.008,0.0003,0.035)或血清(2 例中均无,8 例中均无,5 例中均无;=0.139,0.002,0.009)中均无免疫反应性。脑脊液中 EV 肽抗体水平高于非 AFM 对照组,这支持 EV 感染与 AFM 之间存在关联的合理性,这需要进一步研究,并有可能导致诊断和预防疾病的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6e2/6692520/8df31ee97255/mBio.01903-19-f0001.jpg

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