Immunological evaluation of peptide vaccination for cancer patients with the HLA-A26 allele
- PMID: 26212219
- PMCID: PMC4638024
- DOI: 10.1111/cas.12757
Immunological evaluation of peptide vaccination for cancer patients with the HLA-A26 allele
Abstract
To develop a peptide vaccine for cancer patients with the HLA-A26 allele, which is a minor population worldwide, we investigated the immunological responses of HLA-A26(+) /A26(+) cancer patients to four different CTL epitope peptides under personalized peptide vaccine regimens. In personalized peptide vaccine regimens, two to four peptides showing positive peptide-specific IgG responses in pre-vaccination plasma were selected from the four peptide candidates applicable for HLA-A26(+) /A26(+) cancer patients and administered s.c. Peptide-specific CTL and IgG responses along with cytokine levels were measured before and after vaccination. Cell surface markers in PBMCs and plasma cytokine levels were also measured. In this study, 21 advanced cancer patients, including seven lung, three breast, two pancreas, and two colon cancer patients, were enrolled. Their HLA-A26 genotypes were HLA-A26:01 (n = 24), HLA-A26:03 (n = 10), and HLA-A26:02 (n = 8). One, 14, and 6 patients received two, three, and four peptides, respectively. Grade 1 or 2 skin reactions at the injection sites were observed in the majority of patients, but no severe adverse events related to the vaccination were observed. Peptide-specific CTL responses were augmented in 39% or 22% of patients after one or two cycles of vaccination, respectively. Notably, peptide-specific IgG were augmented in 63% or 100% of patients after one or two cycles of vaccination, respectively. Personalized peptide vaccines with these four CTL epitope peptides could be feasible for HLA-A26(+) advanced cancer patients because of their safety and higher rates of immunological responses.
Keywords: Cancer vaccines; HLA-A26; IgG; cytotoxic T-Lymphocytes; peptide vaccines.
© 2015 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association.
Figures

Similar articles
-
Immunological evaluation of peptide vaccination for cancer patients with the HLA -A11+ or -A33+ allele.Cancer Sci. 2017 Apr;108(4):598-603. doi: 10.1111/cas.13189. Epub 2017 Apr 21. Cancer Sci. 2017. PMID: 28178396 Free PMC article.
-
Phase II study of personalized peptide vaccination for refractory bone and soft tissue sarcoma patients.Cancer Sci. 2013 Oct;104(10):1285-94. doi: 10.1111/cas.12226. Epub 2013 Aug 6. Cancer Sci. 2013. PMID: 23829867 Free PMC article. Clinical Trial.
-
Phase II Study of Personalized Peptide Vaccination with Both a Hepatitis C Virus-Derived Peptide and Peptides from Tumor-Associated Antigens for the Treatment of HCV-Positive Advanced Hepatocellular Carcinoma Patients.J Immunol Res. 2015;2015:473909. doi: 10.1155/2015/473909. Epub 2015 Oct 11. J Immunol Res. 2015. PMID: 26539554 Free PMC article. Clinical Trial.
-
Next-generation peptide vaccines for advanced cancer.Cancer Sci. 2013 Jan;104(1):15-21. doi: 10.1111/cas.12050. Epub 2012 Dec 4. Cancer Sci. 2013. PMID: 23107418 Free PMC article. Review.
-
The use of HLA class I tetramers to design a vaccination strategy for melanoma patients.Immunol Rev. 2002 Oct;188:155-63. doi: 10.1034/j.1600-065x.2002.18814.x. Immunol Rev. 2002. PMID: 12445289 Review.
Cited by
-
Potential association factors for developing effective peptide-based cancer vaccines.Front Immunol. 2022 Jul 27;13:931612. doi: 10.3389/fimmu.2022.931612. eCollection 2022. Front Immunol. 2022. PMID: 35967400 Free PMC article.
-
Predictive factors of the tumor immunological microenvironment for long-term follow-up in early stage breast cancer.Cancer Sci. 2017 Jan;108(1):81-90. doi: 10.1111/cas.13114. Epub 2017 Jan 21. Cancer Sci. 2017. PMID: 27801993 Free PMC article.
-
Uncommon P1 Anchor-featured Viral T Cell Epitope Preference within HLA-A*2601 and HLA-A*0101 Individuals.Immunohorizons. 2024 Jun 1;8(6):415-430. doi: 10.4049/immunohorizons.2400026. Immunohorizons. 2024. PMID: 38885041 Free PMC article.
References
-
- Powles T, Eder JP, Fine GD, et al. MPDL3280A (anti-PD-L1) treatment leads to clinical activity in metastatic bladder cancer. Nature. 2014;515:558–62. - PubMed
-
- Tung NM, Winer EP. Tumor-infiltrating lymphocytes and response to platinum in triple-negative breast cancer. J Clin Oncol. 2015;33:969–71. - PubMed
-
- Noguchi M, Yao A, Harada M, et al. Immunological evaluation of neoadjuvant peptide vaccination before radical prostatectomy for patients with localized prostate cancer. Prostate. 2007;67:933–42. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials