| Literature DB >> 21546493 |
Suzanne van Dorp1, Henrike Resemann, Liane te Boome, Floor Pietersma, Debbie van Baarle, Frits Gmelig-Meyling, Roel de Weger, Eefke Petersen, Monique Minnema, Henk Lokhorst, Saskia Ebeling, Scott J P Beijn, Edward F Knol, Marijke van Dijk, Ellen Meijer, Jürgen Kuball.
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 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(+) 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).Entities:
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Year: 2011 PMID: 21546493 PMCID: PMC3166111 DOI: 10.3324/haematol.2011.041814
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941