Zamecnik Colin R, Sowa Gavin M, Abdelhak Ahmed, Dandekar Ravi, Bair Rebecca D, Wade Kristen J, Bartley Christopher M, Kizer Kerry, Augusto Danillo G, Tubati Asritha, Gomez Refujia, Fouassier Camille, Gerungan Chloe, Caspar Colette M, Alexander Jessica, Wapniarski Anne E, Loudermilk Rita P, Eggers Erica L, Zorn Kelsey C, Ananth Kirtana, Jabassini Nora, Mann Sabrina A, Ragan Nicholas R, Santaniello Adam, Henry Roland G, Baranzini Sergio E, Zamvil Scott S, Sabatino Joseph J, Bove Riley M, Guo Chu-Yueh, Gelfand Jeffrey M, Cuneo Richard, von Büdingen H-Christian, Oksenberg Jorge R, Cree Bruce A C, Hollenbach Jill A, Green Ari J, Hauser Stephen L, Wallin Mitchell T, DeRisi Joseph L, Wilson Michael R
Department of Neurology, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.
University of California, San Francisco School of Medicine, San Francisco, CA, USA.
Nat Med. 2024 May;30(5):1300-1308. doi: 10.1038/s41591-024-02938-3. Epub 2024 Apr 19.
Although B cells are implicated in multiple sclerosis (MS) pathophysiology, a predictive or diagnostic autoantibody remains elusive. In this study, the Department of Defense Serum Repository (DoDSR), a cohort of over 10 million individuals, was used to generate whole-proteome autoantibody profiles of hundreds of patients with MS (PwMS) years before and subsequently after MS onset. This analysis defines a unique cluster in approximately 10% of PwMS who share an autoantibody signature against a common motif that has similarity with many human pathogens. These patients exhibit antibody reactivity years before developing MS symptoms and have higher levels of serum neurofilament light (sNfL) compared to other PwMS. Furthermore, this profile is preserved over time, providing molecular evidence for an immunologically active preclinical period years before clinical onset. This autoantibody reactivity was validated in samples from a separate incident MS cohort in both cerebrospinal fluid and serum, where it is highly specific for patients eventually diagnosed with MS. This signature is a starting point for further immunological characterization of this MS patient subset and may be clinically useful as an antigen-specific biomarker for high-risk patients with clinically or radiologically isolated neuroinflammatory syndromes.
尽管B细胞与多发性硬化症(MS)的病理生理学有关,但预测性或诊断性自身抗体仍然难以捉摸。在本研究中,国防部血清库(DoDSR),一个超过1000万人的队列,被用于生成数百名MS患者(PwMS)在MS发病前数年及发病后数年的全蛋白质组自身抗体谱。该分析在约10%的PwMS中定义了一个独特的聚类,这些患者共享针对一个与许多人类病原体具有相似性的共同基序的自身抗体特征。这些患者在出现MS症状前数年就表现出抗体反应性,并且与其他PwMS相比,血清神经丝轻链(sNfL)水平更高。此外,这种特征随时间保持不变,为临床发病前数年的免疫活跃临床前期提供了分子证据。这种自身抗体反应性在来自另一个新发MS队列的脑脊液和血清样本中得到了验证,在那里它对最终被诊断为MS的患者具有高度特异性。这种特征是对该MS患者亚组进行进一步免疫特征分析的起点,并且作为临床或放射学孤立神经炎症综合征高危患者的抗原特异性生物标志物可能具有临床应用价值。