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Clinical Trial
. 2015 Oct;106(10):1257-63.
doi: 10.1111/cas.12757. Epub 2015 Sep 25.

Immunological evaluation of peptide vaccination for cancer patients with the HLA-A26 allele

Affiliations
Clinical Trial

Immunological evaluation of peptide vaccination for cancer patients with the HLA-A26 allele

Shinjiro Sakamoto et al. Cancer Sci. 2015 Oct.

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.

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Figures

Figure 1
Figure 1
Clinical responses to personalized peptide vaccination (PPV). Computed tomography findings of a patient with stable disease. (a) At diagnosis of lung cancer, 1 year before first vaccination. (b) At recurrence of lung cancer, 3 months before first vaccination. Before this time, the patient had undergone radiation therapy and achieved complete response. (c) One year after first vaccination, the tumor had increased slightly, but stable disease was maintained. Arrows indicate tumur site.

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References

    1. Hodi FS, O’Day SJ, McDermott DF, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med. 2010;363:711–23. - PMC - PubMed
    1. Topalian SL, Hodi FS, Brahmer JR, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med. 2012;366:2443–54. - PMC - PubMed
    1. 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
    1. Tung NM, Winer EP. Tumor-infiltrating lymphocytes and response to platinum in triple-negative breast cancer. J Clin Oncol. 2015;33:969–71. - PubMed
    1. 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

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