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-versushost disease. Overall response rate was 61%. Only responding patients were found to have increased B-cell numbers prior to treatment. B cells had a naïve-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+ Tcell 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). ©2011 Ferrata Storti Foundation.
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van Dorp, S., Resemann, H., te Boome, L., Pietersma, F., van Baarle, D., Gmelig-Meyling, F., … Kuball, J. (2011). The immunological phenotype of rituximab-sensitive chronic graft-versus-host disease: A phase II study. Haematologica, 96(9), 1380–1384. https://doi.org/10.3324/haematol.2011.041814
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