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Origins and diversity of pan-isotype human bone marrow plasma cells.
Pacheco, Gaspar A; Rao, Vishal; Yoo, Duck Kyun; Saghaei, Shahab; Tong, Pei; Kumar, Sachin; Marini-Rapoport, Orlee; Allahyari, Zahra; Moghaddam, Ali S; Esbati, Romina; Alirezaee, Aida; Parnes, Aric; Patil, Sarita U; Wesemann, Duane R.
Afiliación
  • Pacheco GA; Department of Medicine, Division of Allergy and Clinical Immunology, Division of Genetics, Brigham and Women's Hospital; Boston, MA 02115, USA.
  • Rao V; Harvard Medical School; Boston, MA 02115, USA.
  • Yoo DK; The Broad Institute of MIT and Harvard; Cambridge, MA 02124, USA.
  • Saghaei S; The Ragon Institute of MGH, MIT and Harvard; Cambridge, MA 02139, USA.
  • Tong P; Massachusetts Consortium on Pathogen Readiness; Boston, MA 02115, USA.
  • Kumar S; Department of Medicine, Division of Allergy and Clinical Immunology, Division of Genetics, Brigham and Women's Hospital; Boston, MA 02115, USA.
  • Marini-Rapoport O; Harvard Medical School; Boston, MA 02115, USA.
  • Allahyari Z; The Broad Institute of MIT and Harvard; Cambridge, MA 02124, USA.
  • Moghaddam AS; The Ragon Institute of MGH, MIT and Harvard; Cambridge, MA 02139, USA.
  • Esbati R; Massachusetts Consortium on Pathogen Readiness; Boston, MA 02115, USA.
  • Alirezaee A; Department of Medicine, Division of Allergy and Clinical Immunology, Division of Genetics, Brigham and Women's Hospital; Boston, MA 02115, USA.
  • Parnes A; Harvard Medical School; Boston, MA 02115, USA.
  • Patil SU; The Broad Institute of MIT and Harvard; Cambridge, MA 02124, USA.
  • Wesemann DR; The Ragon Institute of MGH, MIT and Harvard; Cambridge, MA 02139, USA.
bioRxiv ; 2024 May 10.
Article en En | MEDLINE | ID: mdl-38766053
ABSTRACT
Bone marrow plasma cells (BMPCs) produce durable, protective IgM, IgG, and IgA antibodies, and in some cases, pro-allergic IgE antibodies, but their properties and sources are unclear. We charted single BMPC transcriptional and clonal heterogeneity in food-allergic and non-allergic individuals across CD19 protein expression given its inverse correlation to BMPC longevity. Transcriptional and clonal diversity revealed distinct functional profiles. Additionally, distribution of somatic hypermutation and intraclonal antibody sequence variance suggest that CD19low and CD19high BMPCs arise from recalled memory and germinal center B cells, respectively. Most IgE BMPCs were from peanut-allergic individuals; two out of 32 from independent donors bound peanut antigens in vitro and in vivo. These findings shed light on BMPC origins and highlight the bone marrow as a source of pathogenic IgE in peanut allergy.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos