Galili Uri
Department of Surgery, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Clin Dev Immunol. 2011;2011:134020. doi: 10.1155/2011/134020. Epub 2011 Nov 17.
Anti-Gal is the most abundant antibody in humans, constituting 1% of immunoglobulins. Anti-Gal binds specifically α-gal epitopes (Galα1-3Galβ1-4GlcNAc-R). Immunogenicity of autologous tumor associated antigens (TAA) is greatly increased by manipulating tumor cells to express α-gal epitopes and bind anti-Gal. Glycolipids with αgal epitopes (α-gal glycolipids) injected into tumors insert into the tumor cell membrane. Anti-Gal binding to the multiple α-gal epitopes de novo presented on the tumor cells results in targeting of these cells to APC via the interaction between the Fc portion of the bound anti-Gal and Fcγ; receptors on APC. The APC process and present immunogenic TAA peptides and thus, effectively activate tumor specific CD4+ helper T cells and CD8+ cytotoxic T cells which destroy tumor cells in micrometastases. The induced immune response is potent enough to overcome immunosuppression by Treg cells. A phase I clinical trial indicated that α-gal glycolipid treatment has no adverse effects. In addition to achieving destruction of micrometastases in cancer patients with advance disease, α-gal glycolipid treatment may be effective as neo-adjuvant immunotherapy. Injection of α-gal glycolipids into primary tumors few weeks prior to resection can induce a protective immune response capable of destroying micrometastases expressing autologous TAA, long after primary tumor resection.
抗半乳糖(Anti-Gal)是人类体内含量最丰富的抗体,占免疫球蛋白的1%。抗半乳糖特异性结合α-半乳糖表位(Galα1-3Galβ1-4GlcNAc-R)。通过操控肿瘤细胞表达α-半乳糖表位并结合抗半乳糖,可大幅增强自体肿瘤相关抗原(TAA)的免疫原性。注入肿瘤的含α-半乳糖表位的糖脂(α-半乳糖糖脂)插入肿瘤细胞膜。抗半乳糖与肿瘤细胞上新呈现的多个α-半乳糖表位结合,通过结合的抗半乳糖的Fc部分与抗原呈递细胞(APC)上的Fcγ受体之间的相互作用,将这些细胞靶向至APC。APC加工并呈递免疫原性TAA肽,从而有效激活肿瘤特异性CD4+辅助性T细胞和CD8+细胞毒性T细胞,这些细胞可破坏微转移灶中的肿瘤细胞。诱导的免疫反应强大到足以克服调节性T细胞(Treg)的免疫抑制作用。一项I期临床试验表明,α-半乳糖糖脂治疗无不良反应。除了能够破坏晚期癌症患者的微转移灶外,α-半乳糖糖脂治疗作为新辅助免疫疗法可能有效。在切除原发肿瘤前几周向原发肿瘤内注射α-半乳糖糖脂,可诱导产生一种保护性免疫反应,在原发肿瘤切除后很长时间内,该反应能够破坏表达自体TAA的微转移灶。