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Updated: Mar 8, 2026

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Transplantation tolerance: don't forget about the B cells
1Section of Transplantation, Department of Surgery, The University of Chicago, Chicago, IL, USA.
Achieving transplantation tolerance is possible, with regulatory B cells (Bregs) and dysfunctional B cells playing key roles. These findings offer new diagnostic and therapeutic strategies for allograft tolerance.
Area of Science:
- Immunology
- Transplantation Science
Background:
- Limited success in achieving indefinite graft survival without immunosuppression.
- B cell signatures implicated in transplantation tolerance.
- Emergence of regulatory B cells (Bregs) suggests a role in tolerance.
Purpose of the Study:
- To review the roles of Bregs and dysfunctional B cells in transplantation tolerance.
- To explore how these cells contribute to graft survival.
- To identify new diagnostic and therapeutic approaches for allograft tolerance.
Main Methods:
- Review of animal and human studies.
- Analysis of B cell signatures and regulatory B cell functions.
- Investigation of follicular regulatory T cells (Tfr) and their impact on B cells.
Main Results:
- Bregs and dysfunctional B cells are implicated in promoting transplantation tolerance.
- Regulatory B cells (Bregs) possess immune-modulatory functions.
- Follicular regulatory T cells (Tfr) can suppress B cell function and induce epigenetic modifications.
Conclusions:
- Bregs and dysfunctional B cells are critical for achieving and maintaining transplantation tolerance.
- Understanding these cellular mechanisms provides a roadmap for new diagnostic biomarkers.
- New therapeutic strategies targeting B cells can be developed to induce allograft tolerance.
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