Johnston D, el Rouby S, Bystryn J C
New York University Department of Dermatology, NY 10016.
Cancer Biother. 1994 Spring;9(1):29-38. doi: 10.1089/cbr.1994.9.29.
Active immunization to B16 melanoma cells or vaccines induces anti-melanoma immune responses in syngeneic mice. The immunogenic antigens stimulating immunity to this tumor have not been identified. In this study we detected several B16 melanoma antigens immunogenic in syngeneic mice using as probes antimelanoma antibodies induced by immunization to B16 melanoma vaccines. These antigens were identified by SDS-PAGE and autoradiographic analysis of specific immunoprecipitates. They were cell-surface components with approximate molecular weights of 41, 46, 50, 75, 80, and 104 KD. All these antigens were expressed by syngeneic and xenogeneic melanomas and by some unrelated syngeneic tumors but not by normal syngeneic cells, xenogeneic melanocytes, or by B16 melanoma cells obtained from fresh tumors or grown in defined medium. The antigens were distinct from murine viral antigens expressed by B16 melanoma cells and from components of the culture medium used to grow cells for vaccine production. These results indicate that several B16 melanoma cell-surface antigens are immunogenic in syngeneic mice. Expression of these antigens appears to be related to malignant transformation as they were found on all melanomas studied, and some other cancers, but not on normal cells.
对B16黑色素瘤细胞或疫苗进行主动免疫可在同基因小鼠中诱导抗黑色素瘤免疫反应。刺激对该肿瘤产生免疫的免疫原性抗原尚未确定。在本研究中,我们使用针对B16黑色素瘤疫苗免疫诱导产生的抗黑色素瘤抗体作为探针,检测了几种在同基因小鼠中具有免疫原性的B16黑色素瘤抗原。通过SDS-PAGE和特异性免疫沉淀物的放射自显影分析鉴定了这些抗原。它们是细胞表面成分,分子量约为41、46、50、75、80和104 KD。所有这些抗原均由同基因和异种黑色素瘤以及一些不相关的同基因肿瘤表达,但正常同基因细胞、异种黑色素细胞或从新鲜肿瘤获得或在限定培养基中生长的B16黑色素瘤细胞不表达。这些抗原与B16黑色素瘤细胞表达的鼠类病毒抗原以及用于生产疫苗的细胞培养基成分不同。这些结果表明,几种B16黑色素瘤细胞表面抗原在同基因小鼠中具有免疫原性。这些抗原的表达似乎与恶性转化有关,因为在所有研究的黑色素瘤以及一些其他癌症中都发现了它们,但在正常细胞中未发现。