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PMID Allele Disease Population Drug Names SNP Class Sentence
14720331 HUMAN LEUKOCYTE ANTIGEN (HUMAN LEUKOCYTE ANTIGEN) prostate cancer NA NA NA unclassified
to evaluate the safety and toxicity of peptide vaccination for patients with metastatic hormone-refractory prostate cancer (hrpc) based on pre-existing peptide-specific cytotoxic t-lymphocyte (ctl) precursors in the circulation, 10 patients positive for human leukocyte antigen (hla)-a2 with metastatic hrpc were enrolled in a phase i study.
14997204 HLA-A*02 prostate cancer NA NA NA only_studied
identification of an hla-a*0201-restricted t-cell epitope derived from the prostate cancer-associated protein prostein.
15129427 HLA-A*24 phosphate NA estramustine NA unclassified
NA
15129427 HUMAN LEUKOCYTE ANTIGEN (HUMAN LEUKOCYTE ANTIGEN) phosphate NA estramustine NA unclassified
NA
15176050 HLA-A*24 prostate cancer NA NA NA unclassified
a prostate stem cell antigen-derived peptide immunogenic in hla-a24- prostate cancer patients.
15176050 HLA-A*24 prostate cancer NA NA NA unclassified
we attempted to identify prostate stem cell antigen (psca)-derived peptides immunogenic in hla-a24+ prostate cancer patients.
15176050 HLA-A*24 prostate cancer NA NA NA unclassified
among three psca peptides, the psca 76-84 peptide most effectively induced peptide-specific cytotoxic t lymphocytes (ctls) from pbmcs of hla-a24+ prostate cancer patients.
15176050 HLA-A*24 prostate cancer NA NA NA positive
the psca 76-84 peptide-stimulated pbmcs showed a significant level of cytotoxicity against prostate cancer cells in an hla-a24-restricted manner.
15289844 HLA-A*02 prostate cancer NA NA NA unclassified
prostate-related antigen-derived new peptides having the capacity of inducing prostate cancer-reactive ctls in hla-a2+ prostate cancer patients.
15289844 HLA (HLA) prostate cancer NA NA NA unclassified
in this study, we attempted to newly identify epitope peptides from these 2 antigens, which are immunogenic in human histocompatibility leukocyte antigen (hla)-a2+ prostate cancer patients.
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