<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Yong Zhang</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018447000</full_dataset_link><submitter_email>nankai1989@foxmail.com</submitter_email><submitter_affiliation>West China Hospital, Sichuan University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Compartment-Specific B-Cell Glycosylation Remodeling Links Inflammatory Signaling to Pathogenic Fc Glycoforms in NMDAR Encephalitis</name><description>our study provides an integrated multi-omics characterization of compartment-specific B-cell N-glycosylation remodeling in anti-NMDAR encephalitis. By combining CSF IgG glycoproteomics with paired single-cell transcriptomics, we identify a coordinated transcriptional reprogramming associated with inflammatory microenvironmental signaling, B-cell differentiation, and altered Fc glycan composition. Importantly, our findings support a model in which increasing antibody biosynthetic demand progressively exceeds the relative capacity for terminal glycan processing during plasma-cell activation, providing a plausible explanation for the discordance between glycosyltransferase transcription and the under-sialylated IgG phenotype observed in poor outcome groups.</description><dates><publication>Sat Jul 18 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD081317</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>