Hilchey Shannon P, Hyrien Ollivier, Mosmann Tim R, Livingstone Alexandra M, Friedberg Jonathan W, Young Faith, Fisher Richard I, Kelleher Raymond J, Bankert Richard B, Bernstein Steven H
James P. Wilmot Cancer Center, Aab Institute of Biomedical Sciences, and Department of Microbiology and Immunology, School of Medicine and Dentistry, University of Rochester, NY 14642, USA.
Blood. 2009 Apr 16;113(16):3809-12. doi: 10.1182/blood-2008-10-185280. Epub 2009 Feb 4.
The incorporation of rituximab, a chimeric anti-CD20 monoclonal antibody, into the therapeutic armamentarium for patients with follicular lymphoma (FL) has significantly improved treatment outcome for such patients. Despite the almost universal application of this therapy, however, its exact mechanism of action has not been completely defined. One proposed mechanism is that of a "vaccinal" effect, whereby FL cell kill by rituximab results in the elicitation of an FL-specific T-cell response. The demonstration that rituximab can even elicit such a response in patients has, to our knowledge, never been shown. We analyzed the response against the immunoglobulin expressed by the FL before and after rituximab monotherapy in 5 FL patients and found an increase in FL idiotype-specific T cells after rituximab in 4 of 5 patients. Our data thus provide "proof of principle" for the ability of passive immunotherapy with rituximab to elicit an active FL-specific cellular response.
将嵌合抗CD20单克隆抗体利妥昔单抗纳入滤泡性淋巴瘤(FL)患者的治疗手段中,显著改善了此类患者的治疗效果。然而,尽管这种疗法几乎被广泛应用,但其确切的作用机制尚未完全明确。一种提出的机制是“疫苗”效应,即利妥昔单抗杀死FL细胞会引发FL特异性T细胞反应。据我们所知,利妥昔单抗甚至能在患者中引发这种反应从未被证实过。我们分析了5例FL患者在利妥昔单抗单药治疗前后针对FL表达的免疫球蛋白的反应,发现5例患者中有4例在使用利妥昔单抗后FL独特型特异性T细胞增加。因此我们的数据为利妥昔单抗被动免疫疗法引发活跃的FL特异性细胞反应的能力提供了“原理证明”。