4.7 Article

Identification of HCC-22-5 tumor-associated antigen and antibody response in patients

Journal

CLINICA CHIMICA ACTA
Volume 366, Issue 1-2, Pages 274-280

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cca.2005.10.026

Keywords

SEREX; HCC-225; tumor associated antigen (TAA); human hepatocellular carcinoma; ELISA

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Background: Serological identification of antigens by recombinant expression cloning (SEREX) is a promising method used to analyze tumor-associated antigen (TAA). Nineteen primary HCC-associated antigens have been found from a HCC cDNA library using autogenous serum by the SEREX approach. We searched for HCC-associated antigens and applied them to HCC diagnosis. Methods: Nine of 19 primaries HCC-associated antigens identified by SEREX method were tested their immune response again with distinct allogeneic sera. One of the screened HCC-associated antigens, HCC-22-5 was recombined and expressed and made the frequency analysis of its seropositivity in various patients using the methods of Western-blot and ELISA. Results: SEREX analysis showed that 9 primary HCC-associated antigens had high-titered 1gG antibody in the majority of HCC patients. Western-Blot method confirmed that 3/7 HCC patients had antibodies against HCC-22-5, which demonstrated that expressed HCC-22-5 antigen had the character of antigen. Sera samples from 341 patients and 80 normal individuals have been tested for autoantibodies against HCC-22-5 by ELISA method. The results found that 51/128 of HCC, 11/76 of chronic hepatitis, 11/22 of liver cirrhosis and 8/54 of nasopharynx cancer patients had antibodies against HCC-22-5. No antibody response to HCC-22-5 had been found in the sera of 7 lung cancers, 54 gastric-intestine patients and 80 normal individuals. The groups of HCC and liver cirrhosis had higher antibody positive rate than that of other groups (p < 0.05). In the HCC sera with alpha-fetoprotein (AFP) negative, the positive rate of HCC-22-5 was as high as 78.9%. Conclusions: HCC-22-5 can be used for HCC serologic screening, especially for the patients with AFP negative. (c) 2005 Elsevier B.V. All rights reserved.

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