| Literature DB >> 24354874 |
M Chesneau1, A Pallier, F Braza, G Lacombe, S Le Gallou, D Baron, M Giral, R Danger, P Guerif, H Aubert-Wastiaux, A Néel, L Michel, D-A Laplaud, N Degauque, J-P Soulillou, K Tarte, S Brouard.
Abstract
Operationally tolerant patients (TOL) display a higher number of blood B cells and transcriptional B cell signature. As they rarely develop an allo-immune response, they could display an abnormal B cell differentiation. We used an in vitro culture system to explore T-dependent differentiation of B cells into plasma cells. B cell phenotype, apoptosis, proliferation, cytokine, immunoglobulin production and markers of differentiation were followed in blood of these patients. Tolerant recipients show a higher frequency of CD20(+) CD24(hi) CD38(hi) transitional and CD20(+) CD38(lo) CD24(lo) naïve B cells compared to patients with stable graft function, correlating with a decreased frequency of CD20(-) CD38(+) CD138(+) differentiated plasma cells, suggestive of abnormal B cell differentiation. B cells from TOL proliferate normally but produce more IL-10. In addition, B cells from tolerant recipients exhibit a defective expression of factors of the end step of differentiation into plasma cells and show a higher propensity for cell death apoptosis compared to patients with stable graft function. This in vitro profile is consistent with down-regulation of B cell differentiation genes and anti-apoptotic B cell genes in these patients in vivo. These data suggest that a balance between B cells producing IL-10 and a deficiency in plasma cells may encourage an environment favorable to the tolerance maintenance. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: Apoptosis; B cells; cytokine; differentiation; tolerance; transplantation
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Year: 2013 PMID: 24354874 DOI: 10.1111/ajt.12508
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086