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白细胞介素-2免疫毒素地尼白介素-妥西毒素可减少调节性T细胞并增强疫苗介导的T细胞免疫。

IL-2 immunotoxin denileukin diftitox reduces regulatory T cells and enhances vaccine-mediated T-cell immunity.

作者信息

Litzinger Mary T, Fernando Romaine, Curiel Tyler J, Grosenbach Douglas W, Schlom Jeffrey, Palena Claudia

机构信息

Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Blood. 2007 Nov 1;110(9):3192-201. doi: 10.1182/blood-2007-06-094615. Epub 2007 Jul 6.

Abstract

CD4+CD25+Foxp3+ regulatory T (Treg) cells have been implicated in the lack of effective antitumor immunity. Denileukin diftitox (DAB(389)IL-2), a fusion protein of interleukin 2 (IL-2) and diphtheria toxin, provides a means of targeting Treg cells. In this study, we examined (1) the effect of denileukin diftitox on the deletion of Treg cells in various lymphoid compartments and (2) the dose scheduling of denileukin diftitox in combination with a recombinant poxviral vaccine to enhance antigen-specific immune responses. Treg cells in spleen, peripheral blood, and bone marrow of normal C57BL/6 mice were variously reduced after a single intraperitoneal injection of denileukin diftitox; the reduction was evident within 24 hours and lasted approximately 10 days. Injection of denileukin diftitox 1 day before vaccination enhanced antigen-specific T-cell responses above levels induced by vaccination alone. These studies show for the first time in a murine model (1) the differential effects of denileukin diftitox on Treg cells in different cellular compartments, (2) the advantage of combining denileukin diftitox with a vaccine to enhance antigen-specific T-cell immune responses, (3) the lack of inhibition by denileukin diftitox of host immune responses directed against a live viral vector, and (4) the importance of dose scheduling of denileukin diftitox when used in combination with a vaccine.

摘要

CD4+CD25+Foxp3+调节性T(Treg)细胞与缺乏有效的抗肿瘤免疫有关。地尼白介素-毒素连接物(DAB(389)IL-2)是白细胞介素2(IL-2)与白喉毒素的融合蛋白,提供了一种靶向Treg细胞的方法。在本研究中,我们检测了:(1)地尼白介素-毒素连接物对不同淋巴区室中Treg细胞缺失的影响;(2)地尼白介素-毒素连接物与重组痘病毒疫苗联合使用时的剂量安排,以增强抗原特异性免疫反应。正常C57BL/6小鼠腹腔内单次注射地尼白介素-毒素连接物后,脾脏、外周血和骨髓中的Treg细胞出现不同程度的减少;这种减少在24小时内明显,持续约10天。在接种疫苗前1天注射地尼白介素-毒素连接物可使抗原特异性T细胞反应增强至高于单独接种疫苗所诱导的水平。这些研究首次在小鼠模型中表明:(1)地尼白介素-毒素连接物对不同细胞区室中Treg细胞的不同作用;(2)地尼白介素-毒素连接物与疫苗联合使用以增强抗原特异性T细胞免疫反应的优势;(3)地尼白介素-毒素连接物不抑制针对活病毒载体的宿主免疫反应;(4)地尼白介素-毒素连接物与疫苗联合使用时剂量安排的重要性。

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