Lynch David H
Bainbridge Biopharma Consulting, Bainbridge Island, WA, USA.
Immunol Rev. 2008 Apr;222:277-86. doi: 10.1111/j.1600-065X.2008.00621.x.
The continuing efforts in biomedical research to develop new therapies for cancer are entering an exciting new phase. Research over the past two to three decades has yielded a much more detailed understanding of the complexities of the cellular and molecular interactions involved in the generation and regulation of immune responses. We are also gaining insights into the mechanisms by which tumors evade or escape immune recognition and by which they become resistant to various existing chemotherapeutic and/or radiotherapeutic strategies. A clear conclusion that can be drawn from these studies is that effective treatments of cancer will become much more multifaceted and will include immunotherapeutic approaches. The identification and molecular cloning of genes encoding the receptors and ligands that play crucial roles in the generation and regulation of immune responses provides exciting new opportunities to induce and enhance effective endogenous immune responses to cancer. In this regard, the genes that comprise the tumor necrosis factor and tumor necrosis factor receptor superfamilies show particular promise. One receptor:ligand pair (4-1BB/CD137 and 4-1BBL/CD137L) is emerging as a target with important potential in its ability to enhance the generation of effective tumor-specific immune responses in situ. The results of the studies cited in this review highlight the potentials of 4-1BB-mediated immunotherapy.
生物医学研究领域为开发癌症新疗法所做的持续努力正进入一个令人兴奋的新阶段。过去二三十年的研究使我们对免疫反应的产生和调节过程中细胞与分子相互作用的复杂性有了更详细的了解。我们也逐渐深入认识肿瘤逃避或逃脱免疫识别的机制,以及它们对各种现有化疗和/或放疗策略产生抗性的机制。从这些研究中可以明确得出的一个结论是,癌症的有效治疗将变得更加多元化,并且将包括免疫治疗方法。对在免疫反应的产生和调节中起关键作用的受体和配体进行基因鉴定和分子克隆,为诱导和增强针对癌症的有效内源性免疫反应提供了令人兴奋的新机会。在这方面,构成肿瘤坏死因子和肿瘤坏死因子受体超家族的基因显示出特别的前景。一对受体-配体(4-1BB/CD137和4-1BBL/CD137L)正成为一个具有重要潜力的靶点,它能够在原位增强有效肿瘤特异性免疫反应的产生。本综述引用的研究结果突出了4-1BB介导的免疫疗法的潜力。