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BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation.

Publication ,  Journal Article
Jia, W; Poe, JC; Su, H; Anand, S; Matsushima, GK; Rathmell, JC; Maillard, I; Radojcic, V; Imai, K; Reyes, NJ; Cardona, DM; Li, Z; Suthers, AN ...
Published in: Blood
May 6, 2021

Patients with chronic graft-versus-host disease (cGVHD) have increased B cell-activating factor (BAFF) levels, but whether BAFF promotes disease after allogeneic bone marrow transplantation (allo-BMT) remains unknown. In a major histocompatibility complex-mismatched model with cGVHD-like manifestations, we first examined B-lymphopenic μMT allo-BMT recipients and found that increased BAFF levels in cGVHD mice were not merely a reflection of B-cell number. Mice that later developed cGVHD had significantly increased numbers of recipient fibroblastic reticular cells with higher BAFF transcript levels. Increased BAFF production by donor cells also likely contributed to cGVHD, because BAFF transcript in CD4+ T cells from diseased mice and patients was increased. cGVHD manifestations in mice were associated with high BAFF/B-cell ratios and persistence of B-cell receptor (BCR)-activated B cells in peripheral blood and lesional tissue. By employing BAFF transgenic (Tg) mice donor cells, we addressed whether high BAFF contributed to BCR activation in cGVHD. BAFF increased NOTCH2 expression on B cells, augmenting BCR responsiveness to surrogate antigen and NOTCH ligand. BAFF Tg B cells had significantly increased protein levels of the proximal BCR signaling molecule SYK, and high SYK protein was maintained by BAFF after in vitro BCR activation or when alloantigen was present in vivo. Using T cell-depleted (BM only) BAFF Tg donors, we found that BAFF promoted cGVHD manifestations, circulating GL7+ B cells, and alloantibody production. We demonstrate that pathologic production of BAFF promotes an altered B-cell compartment and augments BCR responsiveness. Our findings compel studies of therapeutic targeting of BAFF and BCR pathways in patients with cGVHD.

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Published In

Blood

DOI

EISSN

1528-0020

Publication Date

May 6, 2021

Volume

137

Issue

18

Start / End Page

2544 / 2557

Location

United States

Related Subject Headings

  • Transplantation, Homologous
  • T-Lymphocytes
  • Syk Kinase
  • Receptor, Notch2
  • Proto-Oncogene Proteins c-bcr
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Lymphocyte Activation
  • Isoantigens
 

Citation

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MLA
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Jia, W., Poe, J. C., Su, H., Anand, S., Matsushima, G. K., Rathmell, J. C., … Sarantopoulos, S. (2021). BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation. Blood, 137(18), 2544–2557. https://doi.org/10.1182/blood.2020008040
Jia, Wei, Jonathan C. Poe, Hsuan Su, Sarah Anand, Glenn K. Matsushima, Jeffrey C. Rathmell, Ivan Maillard, et al. “BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation.Blood 137, no. 18 (May 6, 2021): 2544–57. https://doi.org/10.1182/blood.2020008040.
Jia W, Poe JC, Su H, Anand S, Matsushima GK, Rathmell JC, et al. BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation. Blood. 2021 May 6;137(18):2544–57.
Jia, Wei, et al. “BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation.Blood, vol. 137, no. 18, May 2021, pp. 2544–57. Pubmed, doi:10.1182/blood.2020008040.
Jia W, Poe JC, Su H, Anand S, Matsushima GK, Rathmell JC, Maillard I, Radojcic V, Imai K, Reyes NJ, Cardona DM, Li Z, Suthers AN, Curry-Chisolm IM, DiCioccio RA, Saban DR, Chen BJ, Chao NJ, Sarantopoulos S. BAFF promotes heightened BCR responsiveness and manifestations of chronic GVHD after allogeneic stem cell transplantation. Blood. 2021 May 6;137(18):2544–2557.

Published In

Blood

DOI

EISSN

1528-0020

Publication Date

May 6, 2021

Volume

137

Issue

18

Start / End Page

2544 / 2557

Location

United States

Related Subject Headings

  • Transplantation, Homologous
  • T-Lymphocytes
  • Syk Kinase
  • Receptor, Notch2
  • Proto-Oncogene Proteins c-bcr
  • Mice, Inbred C57BL
  • Mice, Inbred BALB C
  • Mice
  • Lymphocyte Activation
  • Isoantigens