4.7 Article

Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients

Journal

RHEUMATOLOGY
Volume 60, Issue 12, Pages 5538-5548

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/keab257

Keywords

systemic sclerosis; autologous haematopoietic stem cell transplantation; regulatory B cells; immune reconstitution

Categories

Funding

  1. Sao Paulo Research Foundation [Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)] [2013/08135-2, 2016/24443-7, 2018/20343-3]
  2. Coordination for the Improvement of Higher Education Personnel [Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)] [001]

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The study evaluated the reconstitution of different B cell subsets in SSc patients treated with AHSCT, finding that naive B cell frequencies increased while memory B cell frequencies decreased post-treatment. Some suppressive B cell functions were also observed to recover after AHSCT.
Objectives. The rationale of autologous haematopoietic stem cell transplantation (AHSCT) for autoimmune diseases is that high-dose immunosuppression eradicates autoreactive T and B cells and the infused autologous haematopoietic stem cells promote reconstitution of a naive and self-tolerant immune system. The aim of this study was to evaluate the reconstitution of different B cell subsets, both quantitatively and functionally, in SSc patients treated with AHSCT. Methods. Peripheral blood was harvested from 22 SSc patients before transplantation and at 30, 60, 120, 180 and 360 days post-AHSCT. Immunophenotyping of B cell subsets, B cell cytokine production, signalling pathways and suppressive capacity of regulatory B cells (Bregs) were assessed by flow cytometry. Results. Naive B cell frequencies increased from 60 to 360 days post-AHSCT compared with pre-transplantation. Conversely, memory B cell frequencies decreased during the same period. Plasma cell frequencies transiently decreased at 60 days post-AHSCT. IL-10-producing Bregs CD19(+)CD24(hi)CD38(hi) and CD19(+)CD24(hi)CD27(+) frequencies increased at 180 days. Moreover, the phosphorylation of extracellular signal-regulated kinase 1/2 and p38 mitogen-activated protein kinase increased in B cells reconstituted post-AHSCT. Notably, CD19(+)CD24(hi)CD38(hi) Bregs recovered their ability to suppress production of Th1 cytokines by CD4(+) T cells at 360 days post-AHSCT. Finally, IL-6 and TGF-beta 1-producing B cells decreased following AHSCT. Conclusion. Taken together, these results suggest improvements in immunoregulatory and anti-fibrotic mechanisms after AHSCT for SSc, which may contribute to re-establishment of self-tolerance and clinical remission.

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