Distinct oligoclonal band antibodies in multiple sclerosis recognize ubiquitous self-proteins

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 113; no. 28; pp. 7864 - 7869
• Main Authors: Brändle, Simone M., Obermeier, Birgit, Senel, Makbule, Bruder, Jessica, Mentele, Reinhard, Khademi, Mohsen, Olsson, Tomas, Tumani, Hayrettin, Kristoferitsch, Wolfgang, Lottspeich, Friedrich, Wekerle, Hartmut, Hohlfeld, Reinhard, Dornmair, Klaus
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 12.07.2016
• Series: From the Cover
• Subjects: Antigens; Autoantigens - immunology; Biological Sciences; Borrelia - immunology; HEK293 Cells; Humans; Lyme Neuroborreliosis - immunology; Mass spectrometry; Medicin och hälsovetenskap; Multiple sclerosis; Multiple Sclerosis - immunology; Oligoclonal Bands - immunology; Pathogenesis; Polyclonal antibodies; Proteins; transcriptomics; proteomics; autoantigens; multiple sclerosis; oligoclonal bands
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1522730113

Oligoclonal Ig bands (OCBs) of the cerebrospinal fluid are a hallmark of multiple sclerosis (MS), a disabling inflammatory disease of the central nervous system (CNS). OCBs are locally produced by clonally expanded antigen-experienced B cells and therefore are believed to hold an important clue to the pathogenesis. However, their target antigens have remained unknown, mainly because it was thus far not possible to isolate distinct OCBs against a background of polyclonal antibodies. To overcome this obstacle, we copurified disulfide-linked Ig heavy and light chains from distinct OCBs for concurrent analysis by mass spectrometry and aligned patient-specific peptides to corresponding transcriptome databases. This method revealed the full-length sequences of matching chains from distinct OCBs, allowing for antigen searches using recombinant OCB antibodies. As validation, we demonstrate that an OCB antibody from a patient with an infectious CNS disorder, neuroborreliosis, recognized a Borrelia protein. Next, we produced six recombinant antibodies from four MS patients and identified three different autoantigens. All of them are conformational epitopes of ubiquitous intracellular proteins not specific to brain tissue. Our findings indicate that the B-cell response in MS is heterogeneous and partly directed against intracellular autoantigens released during tissue destruction. In addition to helping elucidate the role of B cells in MS, our approach allows the identification of target antigens of OCB antibodies in other neuroinflammatory diseases and the production of therapeutic antibodies in infectious CNS diseases.