Abstract
The transcriptional regulation of B-cell response to antigen stimulation is complex and involves an intricate network of dynamic signals from cytokines and transcription factors propagated from T-cell interaction. Long-term alloimmunity, in the setting of organ transplantation, is dependent on this B-cell response, which does not appear to be halted by current immunosuppressive regimens which are targeted at T cells. There is emerging evidence that shows that B cells have a diverse response to solid organ transplantation that extends beyond plasma cell antibody production. In this review, we discuss the mechanistic pathways of B-cell activation and differentiation as they relate to the transcriptional regulation of germinal center B cells, plasma cells, and memory B cells in the setting of solid organ transplantation.
Original language | English (US) |
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Article number | 895157 |
Pages (from-to) | 895157 |
Journal | Frontiers in immunology |
Volume | 13 |
DOIs | |
State | Published - Aug 9 2022 |
Keywords
- B cells
- alloimmunity
- rejection
- transcriptional (regulation)
- transplant
- Germinal Center
- B-Lymphocytes
- Graft Rejection
- Organ Transplantation
- Histocompatibility
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology