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PMID Allele Disease Population Drug Names SNP Class Sentence
15289844 HLA-A*02 prostate cancer NA NA NA unclassified
these 2 candidates effectively induced hla-a2-restricted and prostate cancer-reactive ctls in hla-a2+ prostate cancer patients with several hla-a2 subtypes.
15289844 HLA-A*02 prostate cancer NA NA NA unclassified
these results indicate that these psma441-450 and pap112-120 peptides could be promising candidates for peptide-based immunotherapy for hla-a2(+) prostate cancer.
15378520 HLA-A*24 phosphate NA estramustine NA only_studied
NA
15378520 HUMAN LEUKOCYTE ANTIGEN (HUMAN LEUKOCYTE ANTIGEN) phosphate NA estramustine NA only_studied
NA
16000955 HLA-A*24 prostate cancer NA NA NA only_studied
the authors studied humoral and cd4+ t-cell responses in an hla-a24+ prostate cancer patient vaccinated with cytotoxic t lymphocyte (ctl)-directed peptides, including a prostate-specific antigen (psa)248-257 peptide, to understand what kinds of immune responses are elicited in peptide-vaccinated patients.
16203785 HLA-A*03 prostate cancer NA NA NA only_studied
identification of peptide vaccine candidates for prostate cancer patients with hla-a3 supertype alleles.
16203785 HLA-A*33 prostate cancer NA NA NA unclassified
in this study, we attempted to identify ctl-directed peptide candidates, derived from prostate-related antigens and shared by hla-a11+, hla-a31+, and hla-a33+ prostate cancer patients.
16203785 HLA-A*31 prostate cancer NA NA NA unclassified
in this study, we attempted to identify ctl-directed peptide candidates, derived from prostate-related antigens and shared by hla-a11+, hla-a31+, and hla-a33+ prostate cancer patients.
16203785 HLA-A*11 prostate cancer NA NA NA unclassified
in this study, we attempted to identify ctl-directed peptide candidates, derived from prostate-related antigens and shared by hla-a11+, hla-a31+, and hla-a33+ prostate cancer patients.
16203785 HLA-A*33 prostate cancer NA NA NA unclassified
these peptides were first screened for their ability to be recognized by immunoglobulin g (igg) of prostate cancer patients and subsequently for the potential to induce peptide-specific and prostate cancer-reactive ctls from peripheral blood mononuclear cells (pbmc) of cancer patients with the hla-a11, hla-a31, and hla-a33 alleles.
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