Identification of antigen-specific IgG in sera from patients with chronic prostatitis

被引:42
作者
Dunphy, EJ
Eickhoff, JC
Muller, CH
Berger, RE
McNeel, DG
机构
[1] Univ Wisconsin, Ctr Comprehens Canc, Dept Med, Sect Med Oncol, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Biostat, Madison, WI USA
[3] Univ Washington, Dept Urol, Seattle, WA 98195 USA
关键词
antibody; antigens; chronic prostatitis; SEREX; prostate;
D O I
10.1023/B:JOCI.0000040920.96065.5a
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antigen-specific vaccines are one of several molecularly targeted approaches under investigation as possible treatments for prostate cancer. Important to the development of vaccines is the identification of appropriate target antigens. We hypothesized that antigens of the prostate might be identified in patients with the chronic prostatitis/pelvic pain syndrome, a syndrome for which an autoimmune pathology has been proposed. Such antigens might represent naturally recognized target antigens of the prostate that could be investigated in the future as prostate tumor antigens. In this report, we used SEREX to identify proteins expressed in a prostate cDNA expression library recognized by IgG from the sera of patients with chronic prostatitis. Candidate proteins were evaluated using a panel of sera from 62 subjects with symptomatic prostatitis and 71 control male blood donors. We identified one protein that was recognized primarily in sera from subjects with prostatitis compared with controls. MAD-PRO-34, a nucleolar autoantigen, was recognized in 6/62 subjects and 0/71 controls ( p = 0.00897). This protein had previously been identified as an autoantigen in patients with prostate cancer. In addition, the NY-CO-7 protein was recognized in 9/62 subjects and 3/71 controls ( p = 0.0654). Two subjects had IgG specific for both the MAD-PRO-34 and NY-CO-7 gene products. Our results demonstrate that some patients with the chronic prostatitis/ pelvic pain syndrome have autoantibodies to specific proteins. Proteins identified, and MAD-PRO-34 in particular, could be further investigated as potential prostate tumor antigens.
引用
收藏
页码:492 / 502
页数:11
相关论文
共 40 条
[1]   Autoimmune prostatitis: Evidence of T cell reactivity with normal prostatic proteins [J].
Alexander, RB ;
Brady, F ;
Ponniah, S .
UROLOGY, 1997, 50 (06) :893-899
[2]   Autoimmune T cell responses to seminal plasma in chronic pelvic pain syndrome (CPPS) [J].
Batstone, GRD ;
Doble, A ;
Gaston, JSH .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2002, 128 (02) :302-307
[3]  
BOCKER T, 1995, MODERN PATHOL, V8, P226
[4]   THE TYROSINASE GENE CODES FOR AN ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
WOLFEL, C ;
DEPLAEN, E ;
LETHE, B ;
COULIE, P ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :489-495
[5]  
Burch PA, 2000, CLIN CANCER RES, V6, P2175
[6]   Dendritic cell-based xenoantigen vaccination for prostate cancer immunotherapy [J].
Fong, L ;
Brockstedt, D ;
Benike, C ;
Breen, JK ;
Strang, G ;
Ruegg, CL ;
Engleman, EG .
JOURNAL OF IMMUNOLOGY, 2001, 167 (12) :7150-7156
[7]   Identification of nucleolar protein No55 as a tumour-associated autoantigen in patients with prostate cancer [J].
Fosså, A ;
Siebert, R ;
Aasheim, HC ;
Mælandsmo, GM ;
Berner, A ;
Fosså, SD ;
Paus, E ;
Smeland, EB ;
Gaudernack, G .
BRITISH JOURNAL OF CANCER, 2000, 83 (06) :743-749
[8]   Induction of primary NY-ESO-1 immunity:: CD8+T lymphocyte and antibody responses in peptide-vaccinated patients with NY-ESO-1+cancers [J].
Jäger, E ;
Gnjatic, S ;
Nagata, Y ;
Stockert, E ;
Jäger, D ;
Karbach, J ;
Neumann, A ;
Rieckenberg, J ;
Chen, YT ;
Ritter, G ;
Hoffman, E ;
Arand, M ;
Old, LJ ;
Knuth, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12198-12203
[9]   Simultaneous humoral and cellular immune response against cancer-testis antigen NY-ESO-1:: Definition of human histocompatibility leukocyte antigen (HLA)-A2-binding peptide epitopes [J].
Jäger, E ;
Chen, YT ;
Drijfhout, JW ;
Karbach, J ;
Ringhoffer, M ;
Jäger, D ;
Arand, M ;
Wada, H ;
Noguchi, Y ;
Stockert, E ;
Old, LJ ;
Knuth, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (02) :265-270
[10]   CHIP is a U-box-dependent E3 ubiquitin ligase -: Identification of Hsc70 as a target for ubiquitylation [J].
Jiang, JH ;
Ballinger, CA ;
Wu, YX ;
Dai, Q ;
Cyr, DM ;
Höhfeld, J ;
Patterson, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (46) :42938-42944