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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
Regulatory B cells: Development, phenotypes, functions, and role in transplantation
Rowa Y Alhabbab1,2, Estefanía Nova-Lamperti3, Octavio Aravena4
1Infectious Disease Unit and Division of Applied Medical Sciences, King Fahad Centre for medical research, King Abdulaziz University, Jeddah, Saudi Arabia.
Regulatory B cells (Bregs) possess antibody-independent immune-suppressing functions. This review details Breg subsets, development, and roles in inflammation and transplantation, comparing human and animal findings.
Area of Science:
- Immunology
- Cell Biology
Background:
- Early research in the 1970s suggested B cells could inhibit immune responses via antibodies.
- Subsequent studies revealed antibody-independent immunoregulatory functions of B cells.
- Various B cell subsets with regulatory functions have been identified in humans and animals.
Purpose of the Study:
- To review the development pathways of regulatory B cells (Bregs).
- To describe different Breg subsets, their phenotypes, and functions.
- To highlight the role of Bregs in transplantation and compare human and animal studies.
Main Methods:
- Literature review of studies on regulatory B cells.
- Analysis of research on Bregs in inflammation, transplantation, and autoimmunity.
- Comparative analysis of human and animal models.
Main Results:
- Bregs develop through various suggested pathways.
- Distinct Breg subsets with specific phenotypes and functions exist.
- Bregs play a significant role in transplantation, with noted differences between human and animal studies.
Conclusions:
- Regulatory B cells are crucial for immune homeostasis.
- Understanding Breg subsets and their mechanisms is vital for therapeutic applications in autoimmune diseases and transplantation.
- Further research is needed to reconcile findings between human and animal models.
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