Seigler H F, Wallack M K, Vervaert C E, Bash J A, Roberson K M, Stuhlmiller G M
Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710.
J Biol Response Mod. 1989 Feb;8(1):37-52.
Sera from melanoma patients undergoing immunization with three distinct immunogens were evaluated for development of IgG antibody specific for the melanoma tumor-associated antigens (TAAs) GD3 and 250-kd glycoprotein (high molecular weight; HMW). Of 99 patients receiving either irradiated allogeneic melanoma cells admixed with bacillus Calmette-Guérin, vaccinia viral oncolysate melanoma cell membranes, or cholesterol hemisuccinate-modified melanoma cells, 12 were determined to have responded against GD3 and 17 against the HMW TAA. This reactivity was measured using both direct binding to purified TAA and specific inhibition of binding of murine monoclonal antibodies R24 and Me-1-14 for GD3 and HMW TAA, respectively. Preimmune sera from these patients did not react with these TAAs, nor did preimmune sera or follow-up sera from melanoma patients electing not to receive immunotherapy. These results suggest that melanoma patients can be immunized against these TAAs as presented on the melanoma cell membrane in an immunotherapy setting and that immunization using purified TAAs might likewise be feasible.
对接受三种不同免疫原免疫的黑色素瘤患者的血清进行评估,以检测针对黑色素瘤肿瘤相关抗原(TAA)GD3和250-kd糖蛋白(高分子量;HMW)的IgG抗体的产生情况。在99例接受了辐照异体黑色素瘤细胞与卡介苗混合制剂、痘苗病毒溶瘤产物黑色素瘤细胞膜或胆固醇半琥珀酸修饰的黑色素瘤细胞免疫的患者中,有12例被确定对GD3有反应,17例对HMW TAA有反应。这种反应性通过直接与纯化的TAA结合以及分别对鼠单克隆抗体R24和Me-1-14与GD3和HMW TAA的结合进行特异性抑制来测量。这些患者的免疫前血清不与这些TAA发生反应,未选择接受免疫治疗的黑色素瘤患者的免疫前血清或随访血清也不发生反应。这些结果表明,在免疫治疗环境中,黑色素瘤患者可以针对黑色素瘤细胞膜上呈现的这些TAA进行免疫,并且使用纯化的TAA进行免疫同样可能是可行的。