A systematic review of humoral immune responses against tumor antigens

被引:243
作者
Reuschenbach, Miriam [1 ]
Doeberitz, Magnus von Knebel [1 ]
Wentzensen, Nicolas [2 ]
机构
[1] Heidelberg Univ, Dept Appl Tumor Biol, Inst Pathol, D-69120 Heidelberg, Germany
[2] NCI, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
关键词
Humoral immune response; Autoantibodies; Cancer; Tumor antigens; SERUM P53 ANTIBODIES; OVARIAN-CANCER PATIENTS; SQUAMOUS-CELL CARCINOMA; BREAST-CANCER; ANTI-P53; ANTIBODIES; LUNG-CANCER; MUC1; MUCIN; PROSTATE-CANCER; POOR-PROGNOSIS; T-CELL;
D O I
10.1007/s00262-009-0733-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This review summarizes studies on humoral immune responses against tumor-associated antigens (TAAs) with a focus on antibody frequencies and the potential diagnostic, prognostic, and etiologic relevance of antibodies against TAAs. We performed a systematic literature search in Medline and identified 3,619 articles on humoral immune responses and TAAs. In 145 studies, meeting the inclusion criteria, humoral immune responses in cancer patients have been analyzed against over 100 different TAAs. The most frequently analyzed antigens were p53, MUC1, NY-ESO-1, c-myc, survivin, p62, cyclin B1, and Her2/neu. Antibodies against these TAAs were detected in 0-69% (median 14%) of analyzed tumor patients. Antibody frequencies were generally very low in healthy individuals, with the exception of few TAAs, especially MUC1. For several TAAs, including p53, Her2/neu, and NY-ESO-1, higher antibody frequencies were reported when tumors expressed the respective TAA. Antibodies against MUC1 were associated with a favorable prognosis while antibodies against p53 were associated with poor disease outcome. These data suggest different functional roles of endogenous antibodies against TAAs. Although data on prediagnostic antibody levels are scarce and antibody frequencies for most TAAs are at levels precluding use in diagnostic assays for cancer early detection, there is some promising data on achieving higher sensitivity for cancer detection using panels of TAAs.
引用
收藏
页码:1535 / 1544
页数:10
相关论文
共 129 条
[31]  
2-E
[32]   Capitalizing on the immunogenicity of dying tumor cells [J].
Fonseca, Catia ;
Dranoff, Glenn .
CLINICAL CANCER RESEARCH, 2008, 14 (06) :1603-1608
[33]   NY-ESO-1 protein expression and humoral immune responses in prostate cancer [J].
Fosså, A ;
Berner, A ;
Fosså, SD ;
Hernes, E ;
Gaudernack, G ;
Smeland, EB .
PROSTATE, 2004, 59 (04) :440-447
[34]   Level of HER-2/neu protein expression in breast cancer may affect the development of endogenous HER-2/neu-specific immunity [J].
Goodell, Vivian ;
Waisman, James ;
Salazar, Lupe G. ;
dela Rosa, Corazon ;
Link, John ;
Coveler, Andrew L. ;
Childs, Jennifer S. ;
Fintak, Patricia A. ;
Higgins, Doreen M. ;
Disis, Mary L. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (03) :449-454
[35]   POLYMORPHIC EPITHELIAL MUCIN (MUC-1)-CONTAINING CIRCULATING IMMUNE-COMPLEXES IN CARCINOMA PATIENTS [J].
GOUREVITCH, MM ;
VONMENSDORFFPOUILLY, S ;
LITVINOV, SV ;
KENEMANS, P ;
VANKAMP, GJ ;
VERSTRAETEN, AA ;
HILGERS, J .
BRITISH JOURNAL OF CANCER, 1995, 72 (04) :934-938
[36]   Malignancy-induced autoimmunity to MUC1:: initial antibody characterization [J].
Graves, CRL ;
Robertson, JFR ;
Murray, A ;
Price, MR ;
Chapman, CJ .
JOURNAL OF PEPTIDE RESEARCH, 2005, 66 (06) :357-363
[37]   SERUM P53 AUTOANTIBODIES - INCIDENCE IN FAMILIAL BREAST-CANCER [J].
GREEN, JA ;
MUDENDA, B ;
JENKINS, J ;
LEINSTER, SJ ;
TARUNINA, M ;
GREEN, B ;
ROBERTSON, L .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (05) :580-584
[38]   Association of positive serum anti-p53 antibodies with poor prognosis in bladder cancer patients [J].
Gumus, E ;
Erdamar, S ;
Demirel, G ;
Horasanli, K ;
Kendirci, M ;
Miroglu, C .
INTERNATIONAL JOURNAL OF UROLOGY, 2004, 11 (12) :1070-1077
[39]   Circulating anti-MUC1 IgG antibodies as a favorable prognostic factor for pancreatic cancer [J].
Hamanaka, Y ;
Suehiro, Y ;
Fukui, M ;
Shikichi, K ;
Imai, K ;
Hinoda, Y .
INTERNATIONAL JOURNAL OF CANCER, 2003, 103 (01) :97-100
[40]  
Hammel P, 1999, INT J CANCER, V81, P712, DOI 10.1002/(SICI)1097-0215(19990531)81:5<712::AID-IJC7>3.0.CO