Antibodies against oncoproteins E6 and E7 of human papillomavirus types 16 and 18 in patients with head‐and‐neck squamous‐cell carcinoma

• Published in: International journal of cancer Vol. 85; no. 6; pp. 815 - 818
• Main Authors: Zumbach, Klaus, Hoffmann, Markus, Kahn, Tomas, Bosch, Franz, Gottschlich, Stefan, Görögh, Tibor, Rudert, Heinrich, Pawlita, Michael
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 15.03.2000
• Subjects: Adult; AE6 protein; AE7 protein; Aged; Carcinoma, Squamous Cell - blood; Carcinoma, Squamous Cell - virology; DNA, Viral - analysis; Enzyme-Linked Immunosorbent Assay; Female; Head and Neck Neoplasms - blood; Head and Neck Neoplasms - virology; head-and-neck squamous-cell carcinoma; Human papillomavirus 16; Human papillomavirus 18; Humans; Male; Middle Aged; Oncogene Proteins, Viral - blood; Oncogene Proteins, Viral - metabolism; Papillomaviridae - genetics; Papillomaviridae - metabolism
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/(SICI)1097-0215(20000315)85:6<815::AID-IJC14>3.0.CO;2-X

Human papillomaviruses (HPVs) have been recognized as an essential pathogenic factor in anogenital cancer. HPV DNA has also been found in a subgroup of head‐and‐neck squamous‐cell carcinomas (HNSCCs), and a causative role of the virus in the development of these tumors has been suggested by the concomitant inactivation of the tumor‐suppressor protein pRb. Using 4 second‐generation ELISAs, we found antibodies against at least 1 of the oncoproteins E6 and E7 of the high‐risk HPV types 16 and 18 in 11 of 92 sera (12%) taken from HNSCC patients at or near diagnosis, in 1 of 52 sera (2%) taken from HNSCC patients >6 months after diagnosis and in 10 of 288 sera (3.5%) taken from sex‐ and age‐matched healthy control individuals of the normal population. In 11 of the 12 seropositive HNSCC cases, antibodies were directed against HPV16 proteins. In patients, the HPV16 antibodies were mostly of high titer, and in 6 cases, antibodies against both HPV16 oncoproteins were present. Seven of the 8 HPV16 antibody–positive sera from the control group were of low titer, and none of the 10 antibody‐positive sera reacted with both oncoproteins of the same HPV type. The HPV type of the antigens detected by the antibodies in HNSCC patients correlated well with that of the HPV DNA found in the tumor. Of 19 patients known to have HPV16 DNA–positive tumors, 7 (37%) also had HPV16 E6 and/or E7 antibodies. Our finding suggests that the antibodies were formed in an immune response against HPV E6 and E7 proteins expressed in the HNSCC and thus strongly supports the concept of a biologically active role of HPV in the development of a subgroup of HNSCC. Int. J. Cancer 85:815–818, 2000. © 2000 Wiley‐Liss, Inc.