Van den Eynde B
Institut Ludwig pour la Recherche sur le Cancer, Branche de Bruxelles.
Bull Mem Acad R Med Belg. 2007;162(5-6):352-6.
Our scientific activity belongs to tumor immunology: in the last fifteen years, we have contributed to the molecular definition of tumor antigens recognized by cytolytic T lymphocytes, both in human and mice, and to the validation of cancer immunotherapy in appropriate preclinical models. Here we describe two findings that we recently made in this field. The first is the discovery of a new mechanism of production of antigenic peptides, based on the splicing of peptides by the proteasome. The second is the discovery of an important mechanism of tumor resistance to immune rejection. The major interest of this mechanism is that it can be fought with pharmacological agents, which could be used to boost the efficacy of immunotherapy in cancer patients.
在过去的十五年里,我们在人类和小鼠中,对细胞毒性T淋巴细胞识别的肿瘤抗原进行了分子定义,并在合适的临床前模型中验证了癌症免疫疗法。在此,我们描述最近在该领域取得的两项发现。第一项发现是基于蛋白酶体对肽段的剪接作用,发现了一种产生抗原肽的新机制。第二项发现是肿瘤抵抗免疫排斥的一种重要机制。该机制的主要意义在于,可用药物对抗它,这些药物可用于提高癌症患者免疫疗法的疗效。