Identification of Peptide Vaccine Candidates for Prostate Cancer Patients with HLA-A3 Supertype Alleles

التفاصيل البيبلوغرافية
العنوان: Identification of Peptide Vaccine Candidates for Prostate Cancer Patients with HLA-A3 Supertype Alleles
المؤلفون: Mamoru Harada, Kyogo Itoh, Masanori Noguchi, Satoko Matsueda, Hiroko Takedatsu, Akihisa Yao, Masahiro Tanaka
المصدر: Clinical Cancer Research. 11:6933-6943
بيانات النشر: American Association for Cancer Research (AACR), 2005.
سنة النشر: 2005
مصطلحات موضوعية: Glutamate Carboxypeptidase II, Male, Cancer Research, Acid Phosphatase, Amino Acid Motifs, Epitopes, T-Lymphocyte, HLA-A3 Antigen, Cancer Vaccines, Immunoglobulin G, HLA-A11 Antigen, Prostate cancer, Antigen, Prostate, Cell Line, Tumor, medicine, Humans, Alleles, HLA-A Antigens, biology, business.industry, Prostatic Neoplasms, Cancer, Prostate-Specific Antigen, medicine.disease, Protein Structure, Tertiary, Cold Temperature, medicine.anatomical_structure, Oncology, Prostatic acid phosphatase, Antigens, Surface, Immunology, Leukocytes, Mononuclear, Peptide vaccine, biology.protein, Protein Tyrosine Phosphatases, Antibody, Peptides, business, T-Lymphocytes, Cytotoxic
الوصف: Purpose: The peptide vaccine candidates identified to date have been focused on the HLA-A2 and HLA-A24 alleles. The HLA-A11, HLA-A31, and HLA-A33 alleles share binding motifs and belong to an HLA-A3 supertype family. 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.Experimental Design: Based on the binding motif to the HLA-A3 supertype alleles, 42 peptides were prepared from prostate-specific antigen (PSA), prostate-specific membrane antigen (PSMA), and prostatic acid phosphatase (PAP). 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.Results: Five peptide candidates, including the PSA16-24, PAP155-163, PAP248-257, PSMA207-215, and PSMA431-440 peptides, were frequently recognized by IgGs of prostate cancer patients. These peptides efficiently induced peptide-specific and prostate cancer–reactive CTLs from PBMCs of cancer patients with the HLA-A11, HLA-A31, and HLA-A33 alleles. Antibody blocking and cold inhibition experiments revealed that the HLA-A3 supertype–restricted cytotoxicity against prostate cancer cells could be ascribed to peptide-specific and CD8+ T cells.Conclusions: We identified prostate-related antigen-derived new peptide candidates for HLA-A11-, HLA-A31-, and HLA-A33-positive prostate cancer patients. This information could facilitate the development of a peptide-based anticancer vaccine for patients with alleles other than HLA-A2 and HLA-A24.
تدمد: 1557-3265
1078-0432
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0727988e9eadc2e662bbca13c82777b1Test
https://doi.org/10.1158/1078-0432.ccr-05-0682Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....0727988e9eadc2e662bbca13c82777b1
قاعدة البيانات: OpenAIRE