PRETREATMENT AND POSTTREATMENT SERUM ANTIBODY-RESPONSES TO HPV-16-E2-PROTEIN AND HSV-2-ICP8-PROTEIN IN WOMEN WITH CERVICAL-CARCINOMA

被引:27
作者
LEHTINEN, M
LEMINEN, A
KUOPPALA, T
TIIKKAINEN, M
LEHTINEN, T
LEHTOVIRTA, P
PUNNONEN, R
VESTERINEN, E
PAAVONEN, J
机构
[1] UNIV HELSINKI, CENT HOSP, DEPT OBSTET & GYNECOL, SF-00100 HELSINKI 10, FINLAND
[2] UNIV TAMPERE, CENT HOSP, DEPT OBSTET & GYNECOL, TAMPERE, FINLAND
关键词
CERVICAL CANCER; DNA-BINDING PROTEIN; HERPESVIRUS; PAPILLOMAVIRUS; SYNTHETIC PEPTIDE;
D O I
10.1002/jmv.1890370306
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Serum antibodies to early proteins of human papillomavirus type 16 (HPV 16 E2 protein) and herpes simplex virus type 2 (HSV 2 ICP8) can be measured by ELISA. In the serum of 122 newly diagnosed cervical carcinoma patients and age-matched controls, enhanced IgA antibody levels to an HPV-16 E2 protein derived peptide no. 245 indicated a 9.5-fold (95% confidence limits 2.8-57.2) relative risk of cervical carcinoma. No significant risk was found with a corresponding HPV 6 E2 peptide or HSV 2 ICP8. To evaluate the HPV 16 E2 peptide as a possible tumor marker for cervical carcinoma serial postoperative serum samples were tested from 27 women with cervical carcinoma. Antibody responses to the HPV 16 E2 peptide depended on the clinical stage. Stage I and II patients showed decreasing posttreatment IgA and/or IgG antipeptide antibody levels. Stage III and IV patients initially showed decreasing antipeptide antibody levels followed by increasing levels. These patients also showed increasing IgG antibody levels to the HSV 2 ICP8. However, increasing antibody levels to the HPV 16 E2 peptide indicated significantly (P < 0.05) worse 2-year disease free survival (recurring disease) than did stable or decreasing antibody levels. The results suggest that serum antipeptide antibodies to the HPV 16 E2 peptide no. 245 can be used for the monitoring of cervical carcinoma.
引用
收藏
页码:180 / 186
页数:7
相关论文
共 33 条
[1]   STRUCTURAL AND TRANSCRIPTIONAL ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPE-16 SEQUENCES IN CERVICAL-CARCINOMA CELL-LINES [J].
BAKER, CC ;
PHELPS, WC ;
LINDGREN, V ;
BRAUN, MJ ;
GONDA, MA ;
HOWLEY, PM .
JOURNAL OF VIROLOGY, 1987, 61 (04) :962-971
[2]  
BRESLOW NE, 1980, IARC SCI PUBLICAT 32, V1
[3]  
BRINTON LA, 1987, CANCER RES, V47, P1706
[4]  
BUCKLEY JD, 1981, LANCET, V2, P1010
[5]   PRESENCE OF CATENATED HUMAN PAPILLOMAVIRUS TYPE-16 EPISOMES IN A CERVICAL-CARCINOMA CELL-LINE [J].
CHOO, KB ;
CHEUNG, WF ;
LIEW, LN ;
LEE, HH ;
HAN, SH .
JOURNAL OF VIROLOGY, 1989, 63 (02) :782-789
[6]   ANALYSIS OF THE PHYSICAL STATE OF DIFFERENT HUMAN PAPILLOMAVIRUS DNAS IN INTRAEPITHELIAL AND INVASIVE CERVICAL NEOPLASM [J].
CULLEN, AP ;
REID, R ;
CAMPION, M ;
LORINCZ, AT .
JOURNAL OF VIROLOGY, 1991, 65 (02) :606-612
[7]   A SYNTHETIC PEPTIDE DEFINES A SEROLOGIC IGA RESPONSE TO A HUMAN PAPILLOMAVIRUS-ENCODED NUCLEAR ANTIGEN EXPRESSED IN VIRUS-CARRYING CERVICAL NEOPLASIA [J].
DILLNER, J ;
DILLNER, L ;
ROBB, J ;
WILLEMS, J ;
JONES, I ;
LANCASTER, W ;
SMITH, R ;
LERNER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (10) :3838-3841
[8]   MAPPING OF LINEAR EPITOPES OF HUMAN PAPILLOMAVIRUS TYPE-16 - THE E1, E2, E4, E5, E6 AND E7 OPEN READING FRAMES [J].
DILLNER, J .
INTERNATIONAL JOURNAL OF CANCER, 1990, 46 (04) :703-711
[9]   SEROLOGICAL RESPONSES TO PAPILLOMAVIRUS GROUP-SPECIFIC ANTIGENS IN WOMEN WITH NEOPLASIA OF THE CERVIX UTERI [J].
DILLNER, L ;
MORENOLOPEZ, J ;
DILLNER, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :624-627
[10]   DETECTION OF IGA ANTIBODIES AGAINST HUMAN PAPILLOMAVIRUS IN CERVICAL SECRETIONS FROM PATIENTS WITH CERVICAL INTRAEPITHELIAL NEOPLASIA [J].
DILLNER, L ;
BEKASSY, Z ;
JONSSON, N ;
MORENOLOPEZ, J ;
BLOMBERG, J .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (01) :36-40