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IgG responses to tissue-associated antigens as biomarkers of immunological treatment efficacy.
Smith, Heath A; Maricque, Brett B; Eberhardt, John; Petersen, Benjamin; Gulley, James L; Schlom, Jeffrey; McNeel, Douglas G.
Affiliation
  • Smith HA; Carbone Comprehensive Cancer Center, University of Wisconsin, 1111 Highland Avenue, Madison, WI 53705, USA.
J Biomed Biotechnol ; 2011: 454861, 2011.
Article in En | MEDLINE | ID: mdl-21197272
ABSTRACT
We previously demonstrated that IgG responses to a panel of 126 prostate tissue-associated antigens are common in patients with prostate cancer. In the current report we questioned whether changes in IgG responses to this panel might be used as a measure of immune response, and potentially antigen spread, following prostate cancer-directed immune-active therapies. Sera were obtained from prostate cancer patients prior to and three months following treatment with androgen deprivation therapy (n = 34), a poxviral vaccine (n = 31), and a DNA vaccine (n = 21). Changes in IgG responses to individual antigens were identified by phage immunoblot. Patterns of IgG recognition following three months of treatment were evaluated using a machine-learned Bayesian Belief Network (ML-BBN). We found that different antigens were recognized following androgen deprivation compared with vaccine therapies. While the number of clinical responders was low in the vaccine-treated populations, we demonstrate that ML-BBN can be used to develop potentially predictive models.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Immunoglobulin G / Biomarkers, Tumor / Antigens, Neoplasm Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: J Biomed Biotechnol Journal subject: BIOTECNOLOGIA / MEDICINA Year: 2011 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Immunoglobulin G / Biomarkers, Tumor / Antigens, Neoplasm Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: J Biomed Biotechnol Journal subject: BIOTECNOLOGIA / MEDICINA Year: 2011 Document type: Article Affiliation country: Estados Unidos