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一种跨物种黑色素瘤相关抗原在正常和肿瘤性人体组织中的分布。

Distribution of a cross-species melanoma-associated antigen in normal and neoplastic human tissues.

作者信息

Natali P, Bigotti A, Cavalieri R, Wakabayaski S, Taniguchi M, Ferrone S

出版信息

J Invest Dermatol. 1985 Oct;85(4):340-6. doi: 10.1111/1523-1747.ep12276944.

Abstract

In previous studies the monoclonal antibody (MoAb) M2590 elicited in C57/BL6 mice with the syngeneic melanoma cell line B16 has been shown to recognize a 31K glycoprotein expressed by human melanoma cell lines. The present study has shown that the MoAb M2590 cross-reacts with surgically removed benign and malignant lesions of melanocyte origin. The reactivity pattern of the MoAb M2590 with these lesions is different from that of the anti-high-molecular weight-melanoma associated antigen (HMW-MAA) MoAb 225.28S, of the anti-115K MAA MoAb 345.134S, and of the anti-100K MAA MoAb 376.96S, which were elicited with human melanoma cell lines. In particular, the MoAb M2590 reacts with blue nevi. The MoAb M2590-defined MAA, like other types of MAA, is heterogeneous in lesions removed from different patients, in autologous lesions removed from different anatomic sites, and in cells within a lesion. The distribution of the MoAb M2590-defined MAA in normal tissues and in tumors of nonmelanocyte origin is broader than that of the HMW-MAA, but is similar to that of the 115K MAA and of the 100K MAA. The results of this investigation suggest that immunization with xenogeneic melanoma cells may broaden the range of specificity of antihuman MAA MoAbs and provide information about the phylogenetic evolution of MAAs.

摘要

在先前的研究中,用同基因黑色素瘤细胞系B16在C57/BL6小鼠中诱导产生的单克隆抗体(MoAb)M2590已被证明可识别由人黑色素瘤细胞系表达的一种31K糖蛋白。本研究表明,MoAb M2590与手术切除的黑色素细胞起源的良性和恶性病变发生交叉反应。MoAb M2590与这些病变的反应模式不同于用人黑色素瘤细胞系诱导产生的抗高分子量黑色素瘤相关抗原(HMW-MAA)MoAb 225.28S、抗115K MAA MoAb 345.134S和抗100K MAA MoAb 376.96S。特别是,MoAb M2590与蓝色痣发生反应。MoAb M2590定义的MAA与其他类型的MAA一样,在从不同患者切除的病变、从不同解剖部位切除的自体病变以及病变内的细胞中是异质性的。MoAb M2590定义的MAA在正常组织和非黑色素细胞起源的肿瘤中的分布比HMW-MAA更广泛,但与115K MAA和100K MAA相似。本研究结果表明,用异种黑色素瘤细胞免疫可能会拓宽抗人MAA MoAb的特异性范围,并提供有关MAA系统发育进化的信息。

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