Jahrsdörfer Bernd, Weiner George J
Holden Comprehensive Cancer Center, Department of Internal Medicine, Interdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, USA.
Semin Oncol. 2003 Aug;30(4):476-82. doi: 10.1016/s0093-7754(03)00236-7.
Synthetic oligodeoxynucleotides containing CG motifs (CpG ODN) have potent immunostimulatory properties, and have potential as immunotherapeutic agents in cancer. Animal models suggest CpG ODN can activate a variety of immune effector cells such as natural killer (NK) cells, and also enhance the efficacy of tumor immunization when used as immune adjuvants or to directly activate antigen-presenting cells. CpG ODN are also capable of altering the expression of a number of antigens by malignant B-cells, including those targeted by monoclonal antibodies (moAbs) and those involved in communication with T cells. The ability of CpG ODN to activate the immune effector cells that participate in antibody-dependent cellular cytotoxicity (ADCC), upregulate target antigen, and perhaps induce development of an active immune response, suggest these agents may be capable of enhancing the efficacy of antitumor moAb therapy. Such enhanced efficacy has been demonstrated in animal models and is now undergoing evaluation in clinical trials.
含有CG基序的合成寡脱氧核苷酸(CpG ODN)具有强大的免疫刺激特性,在癌症免疫治疗中具有潜在应用价值。动物模型表明,CpG ODN可激活多种免疫效应细胞,如自然杀伤(NK)细胞,并且在用作免疫佐剂或直接激活抗原呈递细胞时,还能增强肿瘤免疫的疗效。CpG ODN还能够改变恶性B细胞多种抗原的表达,包括那些单克隆抗体(moAb)靶向的抗原以及参与与T细胞通讯的抗原。CpG ODN激活参与抗体依赖性细胞毒性(ADCC)的免疫效应细胞、上调靶抗原以及可能诱导主动免疫反应发展的能力,表明这些药物可能能够增强抗肿瘤单克隆抗体治疗的疗效。这种增强的疗效已在动物模型中得到证实,目前正在临床试验中进行评估。