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多发性硬化症疫苗接种患者对新冠病毒Delta变异株刺突蛋白的体液和细胞反应

Humoral and Cellular Response to Spike of Delta SARS-CoV-2 Variant in Vaccinated Patients With Multiple Sclerosis.

作者信息

Petrone Linda, Tortorella Carla, Aiello Alessandra, Farroni Chiara, Ruggieri Serena, Castilletti Concetta, Meschi Silvia, Cuzzi Gilda, Vanini Valentina, Palmieri Fabrizio, Prosperini Luca, Haggiag Shalom, Galgani Simona, Grifoni Alba, Sette Alessandro, Gasperini Claudio, Nicastri Emanuele, Goletti Delia

机构信息

Translational Research Unit, National Institute for Infectious Diseases Lazzaro Spallanzani-IRCCS, Rome, Italy.

Department of Neurosciences, San Camillo-Forlanini Hospital, Rome, Italy.

出版信息

Front Neurol. 2022 May 31;13:881988. doi: 10.3389/fneur.2022.881988. eCollection 2022.

Abstract

OBJECTIVES

We assessed vaccination-induced antibody and cellular response against spike from the ancestral strain and from the Delta Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) variant in patients with Multiple Sclerosis (MS) treated with disease modifying treatments.

METHODS

We enrolled 47 patients with MS and nine controls ("no MS") having completed the vaccination schedule within 4-6 months from the first dose. The Interferon (IFN)-γ-response to spike peptides derived from the ancestral and the Delta SARS-CoV-2 was measured by enzyme-linked immunoassay (ELISA). Anti-Receptor Binding Domain (RBD) IgG were also evaluated.

RESULTS

No significant differences were found comparing the IFN-γ-specific immune response between MS and "no MS" subjects to the ancestral ( = 0.62) or Delta peptide pools ( = 0.68). Nevertheless, a reduced IFN-γ-specific response to the ancestral or to the Delta pools was observed in subjects taking fingolimod or cladribine compared to subjects treated with ocrelizumab or IFN-β. The antibody response was significantly reduced in patients with MS compared to "no MS" subjects ( = 0.0452) mainly in patients taking ocrelizumab or fingolimod.

CONCLUSIONS

Cellular responses to Delta SARS-CoV-2 variant remain largely intact in patients with MS. However, the magnitude of these responses depends on the specific therapy.

摘要

目的

我们评估了接受疾病修饰治疗的多发性硬化症(MS)患者针对原始毒株和德尔塔严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体刺突蛋白的疫苗诱导抗体和细胞反应。

方法

我们招募了47例MS患者和9名对照(“无MS”),他们在从第一剂开始的4 - 6个月内完成了疫苗接种计划。通过酶联免疫吸附测定(ELISA)测量对源自原始毒株和德尔塔SARS-CoV-2的刺突肽的干扰素(IFN)-γ反应。还评估了抗受体结合域(RBD)IgG。

结果

比较MS患者和“无MS”受试者对原始毒株(P = 0.62)或德尔塔肽库(P = 0.68)的IFN-γ特异性免疫反应,未发现显著差异。然而,与接受奥瑞珠单抗或IFN-β治疗的受试者相比,服用芬戈莫德或克拉屈滨的受试者对原始毒株或德尔塔肽库的IFN-γ特异性反应降低。与“无MS”受试者相比,MS患者的抗体反应显著降低(P = 0.0452),主要是服用奥瑞珠单抗或芬戈莫德的患者。

结论

MS患者对德尔塔SARS-CoV-2变体的细胞反应在很大程度上保持完整。然而,这些反应的强度取决于具体治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8b2/9194677/985592108af4/fneur-13-881988-g0001.jpg

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