Department of Immunology, UMC Utrecht, Utrecht, The Netherlands.
Haematologica. 2011 Sep;96(9):1380-4. doi: 10.3324/haematol.2011.041814. Epub 2011 May 5.
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).
慢性移植物抗宿主病是异基因干细胞移植后的主要长期并发症,目前的治疗方法反应率不理想。因此,在一项前瞻性 2 期研究中,评估了利妥昔单抗治疗类固醇难治性慢性移植物抗宿主病患者的临床疗效和淋巴细胞亚群的变化。总体缓解率为 61%。仅发现应答患者在治疗前 B 细胞数量增加。B 细胞具有幼稚抗原呈递表型,主要为 CD5 阴性或 CD5 表达水平较低。在利妥昔单抗治疗一年后,应答患者的正常 B 细胞稳态得到重建,并伴有皮肤浸润的 CD8(+)T 细胞显著下降,表明宿主 B 细胞在维持病理性 CD8(+)T 细胞反应中发挥作用。B 细胞稳态失衡可用于预先识别对利妥昔单抗治疗反应更高的患者(Eudra-CT 2008-004125-42)。