Abstract
Chronic graft-versus-host disease is the major long-term complication after allogeneic stem cell transplantation with a suboptimal response rate to current treatments. Therefore, clinical efficacy and changes in lymphocyte subsets before and after rituximab treatment were evaluated in a prospective phase II study in patients with steroid-refractory chronic graft-versus-host disease. Overall response rate was 61%. Only responding patients were found to have increased B-cell numbers prior to treatment. B cells had a naive-antigen-presenting phenotype and were mainly CD5 negative or had a low CD5 expression. Normal B-cell homeostasis was reestablished in responding patients one year after ritxumab treatment and associated with a significant decline in skin-infiltrating CD8(+) T cells, suggesting that host B cells play a role in maintaining pathological CD8(+) T-cell responses. Imbalances in B-cell homeostasis could be used to identify patients a priori with a higher chance of response to rituximab treatment (Eudra-CT 2008-004125-42).
Original language | English |
---|---|
Pages (from-to) | 1380-1384 |
Number of pages | 5 |
Journal | Haematologica |
Volume | 96 |
Issue number | 9 |
DOIs | |
Publication status | Published - Sept 2011 |
Keywords
- graft-versus-host-disease
- B cell
- rituximab
- transplantation
- STEM-CELL TRANSPLANTATION
- CONSENSUS DEVELOPMENT PROJECT
- WORKING GROUP-REPORT
- CLINICAL-TRIALS
- B-CELLS
- MONOCLONAL-ANTIBODY
- CHRONIC GVHD
- AUTOIMMUNITY
- CHIMERISM
- CRITERIA