Impaired B-cell reconstitution in lymphoma patients undergoing allogeneic HSCT: an effect of pretreatment with rituximab?

被引:16
作者
Buser, A. [1 ,2 ]
Stern, M. [2 ]
Arber, C. [2 ]
Medinger, M. [2 ]
Halter, J. [2 ]
Rovo, A. [2 ]
Favre, G. [3 ]
Lohri, A. [3 ]
Tichelli, A. [2 ]
Gratwohl, A. [2 ]
机构
[1] Swiss Red Cross, Ctr Blood Transfus, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Med, CH-4031 Basel, Switzerland
[3] Med Univ Clin, Kantonsspital, Dept Oncol, Liestal, Switzerland
关键词
allogeneic transplantation; lymphoma; rituximab;
D O I
10.1038/bmt.2008.229
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Allogeneic hematopoietic SCT (HSCT) is increasingly considered an option in refractory or relapsing lymphoma. Today, most patients with B-cell lymphoma are treated with the monoclonal anti-CD20 antibody rituximab before HSCT. We hypothesized that prior therapy with rituximab might alter immune reconstitution after allogeneic transplantation due to in vivo depletion of B cells at the time of graft infusion. We studied B-cell immune reconstitution in 12 patients with lymphoma receiving rituximab 1-12 months before HSCT. Compared to an age- and sex-matched population of patients transplanted for myeloid malignancies, lymphoma patients with rituximab pretreatment showed significantly reduced B-cell counts at time of HSCT at + 3, + 6 and + 12 months; B-cell counts reached values comparable to controls only 24 months after HSCT. In parallel, levels of immunoglobulins were markedly reduced for up to 2 years post transplant in patients with prior rituximab treatment. Two patients suffered from severe late bacterial infections to which the impaired humoral immunity may have contributed. In contrast, T- and NK-cell reconstitution was not different compared to control patients. In conclusion, B-cell reconstitution can be significantly delayed in allogeneic HSCT recipients with prior rituximab treatment. Rituximab appears to have clinical consequences beyond the immediate early post-transplant period.
引用
收藏
页码:483 / 487
页数:5
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