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Toll样受体激动剂在慢性淋巴细胞白血病治疗中的应用

Toll-like receptor agonists in the treatment of chronic lymphocytic leukemia.

作者信息

Spaner D E, Masellis A

机构信息

Division of Molecular and Cellular Biology, Research Institute, Sunnybrook and Women's College Health Sciences Center, Toronto, Ontario, Canada.

出版信息

Leukemia. 2007 Jan;21(1):53-60. doi: 10.1038/sj.leu.2404456. Epub 2006 Oct 26.

DOI:10.1038/sj.leu.2404456
PMID:17066089
Abstract

Advances in our understanding of the Toll-like receptors (TLRs) have led to the identification of several agonists that are suitable for clinical development. Chronic lymphocytic leukemia (CLL) may be especially amenable to TLR agonists because it is an immunologically susceptible tumor with strong expression of several TLRs, particularly TLR-7 and TLR-9. TLR agonists may indirectly clear CLL cells by enhancing the activity of natural killer and tumor-reactive T cells, or by altering the tumor microenvironment and inhibiting angiogenesis. However, signaling pathways can be activated directly in CLL cells by TLR-7 and TLR-9 agonists, leading to the production of cytokines and costimulatory molecules in a manner that is dependent on the underlying cytogenetic abnormalities, but rendering the tumor cells more sensitive to killing by cytotoxic T cells, immunotoxins and some chemotherapeutic drugs. Imidazoquinolines are TLR-7 agonists with strong local activity against CLL, and phase I trials of systemically administered imidazoquinolines (and also cytosine-phosphate-guanosine oligonucleotides that are TLR-9 agonists) are currently ongoing at different centers. The potential importance of these TLR agonists in the treatment of CLL is suggested by their ability to sensitize tumor cells to cytotoxic agents, and their future probably lies in combination with radiotherapies, chemotherapies, monoclonal antibodies and cancer vaccines.

摘要

我们对Toll样受体(TLR)认识的进展,已促使人们鉴定出几种适合临床开发的激动剂。慢性淋巴细胞白血病(CLL)可能对TLR激动剂特别敏感,因为它是一种免疫易感肿瘤,多种TLR,尤其是TLR-7和TLR-9有很强的表达。TLR激动剂可能通过增强自然杀伤细胞和肿瘤反应性T细胞的活性,或通过改变肿瘤微环境和抑制血管生成来间接清除CLL细胞。然而,TLR-7和TLR-9激动剂可直接在CLL细胞中激活信号通路,导致细胞因子和共刺激分子的产生,其方式取决于潜在的细胞遗传学异常,但会使肿瘤细胞对细胞毒性T细胞、免疫毒素和某些化疗药物的杀伤更敏感。咪唑喹啉是对CLL有强大局部活性的TLR-7激动剂,目前不同中心正在进行全身给药咪唑喹啉(以及作为TLR-9激动剂的胞嘧啶-磷酸-鸟苷寡核苷酸)的I期试验。这些TLR激动剂使肿瘤细胞对细胞毒性药物敏感的能力,表明了它们在CLL治疗中的潜在重要性,其未来可能在于与放射疗法、化学疗法、单克隆抗体和癌症疫苗联合使用。

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