Large scale identification of human hepatocellular carcinoma-associated antigens by autoantibodies

被引:155
作者
Wang, Y
Han, KJ
Pang, XW
Vaughan, HA
Qu, W
Dong, XY
Peng, JR
Zhao, HT
Rui, JA
Leng, XS
Cebon, J
Burgess, AW
Chen, WF
机构
[1] Peoples Hosp, Sch Basic Med Sci, Dept Immunol, Beijing, Peoples R China
[2] Peoples Hosp, Ctr Hepatobiliary Surg, Beijing, Peoples R China
[3] Peking Univ, Hlth & Environm Sci, Liver Canc Res Ctr, Affiliated Hosp 8, Beijing 100871, Peoples R China
[4] Univ Melbourne, Royal Melbourne Hosp, Ludwig Inst Canc Res, Melbourne Branch, Melbourne, Vic 3050, Australia
关键词
D O I
10.4049/jimmunol.169.2.1102
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoantibodies are often detected in hepatocellular carcinoma (HCC), and these responses may represent recognition of tumor Ags that are associated with transformation events. The identities of these Ags, however, are less well known. Using serological analysis of recombinant cDNA expression libraries (SEREX) from four HCC patients, we identified 55 independent cDNA sequences potentially encoding HCC tumor Ags. Of these genes, 15 are novel. Two such proteins, HCA587 and HCA661, were predominantly detected in testis, but not in other normal tissues, except for a weak expression in normal pancreas. In addition to HCC, these two Ags can be found in cancers of other histological types. Therefore, they can be categorized as cancer-testis (CT) Ags. Two other Ags (HCA519 and HCA,90) were highly overexpressed in HCC and also expressed in cancer cell lines of lung, prostate, and pancreas, but not in the respective normal tissues. Four other Ags were identified to be expressed in particular types of cancer cell lines (HCA520 in an ovarian cancer cell line, HCA59 and HCA67 in a colon cancer cell line, HCA58 in colon and ovarian cancer cell lines), but not in the normal tissue counterpart(s). In addition, abundant expression of complement inactivation factors was found in HCC. These results indicate a broad range expression of autoantigens in HCC patients. Our findings open an avenue for the study of autoantigens in the transformation, metastasis, and immune evasion in HCC.
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页码:1102 / 1109
页数:8
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