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SARS-CoV-2 specific plasma cells acquire the phenotype of long-lived plasma cells in the human bone marrow
Axel Ronald Schulz; Heike Hirseland; Lisa-Marie Diekmann; Simon Reinke; Sebastian Hardt; Antonia Niedobitek; Henrik E Mei.
Affiliation
  • Axel Ronald Schulz; Germany Rheumatism Research Center Berlin (DRFZ)
  • Heike Hirseland; Germany Rheumatism Research Center Berlin (DRFZ)
  • Lisa-Marie Diekmann; German Rheumatism Research Center Berlin (DRFZ)
  • Simon Reinke; Berlin Institute of Health (BIH)
  • Sebastian Hardt; Charite Universitaetsmedizin Berlin
  • Antonia Niedobitek; German Rheumatism Research Center Berlin (DRFZ)
  • Henrik E Mei; German Rheumatism Research Center Berlin (DRFZ)
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-503574
ABSTRACT
Establishment of long-lived plasma cells (PC) in the bone marrow (BM) is important for the development of long-term specific humoral immunity. While SARS-CoV-2-specific, resting, affinity-matured, IgG-secreting plasma cells were described in human bone marrow approx. 6-7 months after infection or vaccination, the long-term durability of these PC remains unclear. We here show that approximately 20% of SARS-CoV-2-specific human BM plasma cells, including RBD-specific PC accommodate the phenotype of long-lived plasma cells, characterized by the lack of CD19 and/or CD45. This result provides evidence in support of the emergence of persistent SARS-CoV-2 specific plasma cells in humans sustaining the durable production of specific serum IgG protecting against severe courses of COVID-19.
License
cc_by_nc_nd
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2022 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2022 Document type: Preprint