首页> 美国卫生研究院文献>British Journal of Cancer >pMel17 is recognised by monoclonal antibodies NKI-beteb HMB-45 and HMB-50 and by anti-melanoma CTL.
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pMel17 is recognised by monoclonal antibodies NKI-beteb HMB-45 and HMB-50 and by anti-melanoma CTL.

机译:pMel17被单克隆抗体NKI-betebHMB-45和HMB-50和抗黑素瘤CTL识别。

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摘要

Recently, we cloned the cDNA encoding the melanocyte lineage-specific antigen gp100 and demonstrated that gp100 is recognised by three different monoclonal antibodies (MAbs) used to diagnose malignant melanoma. In addition, we showed that tumour-infiltrating lymphocytes (TIL 1200) from a melanoma patient reacted specifically with cells transfected with the gp100 cDNA. Molecular characterisation of the gp100 cDNA revealed that the gp100 antigen is highly homologous, but not identical, to another melanocyte-specific protein, pMel17. Here, we report that cells transfected with pMel17 cDNA also react with all three MAbs used to diagnose malignant melanoma, NKI-beteb, HMB-45 and HMB-50. Moreover, pMel17 transfectants are specifically lysed by TIL1200. These data demonstrate that antigenic processing of both gp100 and pMel17 give rise to peptides seen by anti-melanoma cytotoxic T lymphocytes (CTL) and are therefore potential targets for immunotherapy of malignant melanoma.
机译:最近,我们克隆了编码黑素细胞谱系特异性抗原gp100的cDNA,并证明gp100被用于诊断恶性黑素瘤的三种不同单克隆抗体(MAb)识别。另外,我们显示了来自黑色素瘤患者的肿瘤浸润淋巴细胞(TIL 1200)与转染了gp100 cDNA的细胞发生了特异性反应。 gp100 cDNA的分子特征表明,gp100抗原与另一种黑素细胞特异性蛋白pMel17高度同源,但不完全相同。在这里,我们报告说,转染了pMel17 cDNA的细胞也与用于诊断恶性黑色素瘤的所有三种单克隆抗体(NKI-beteb,HMB-45和HMB-50)反应。而且,pMel17转染子被TIL1200特异性裂解。这些数据表明,对gp100和pMel17的抗原加工都产生了抗黑素瘤细胞毒性T淋巴细胞(CTL)所见的肽,因此是恶性黑素瘤免疫治疗的潜在靶标。

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