Peptide vaccine with glucopyranosyl lipid A-stable oil-in-water emulsion for patients with resected melanoma

被引:7
|
作者
Grewal, Eric P. [1 ]
Erskine, Courtney L. [2 ]
Nevala, Wendy K. [3 ]
Allred, Jacob B. [4 ]
Strand, Carrie A. [4 ]
Kottschade, Lisa A. [1 ]
McWilliams, Robert R. [1 ]
Dronca, Roxana S. [5 ]
Yakovich, Adam J. [6 ]
Markovic, Svetomir N. [1 ]
Block, Matthew S. [1 ]
机构
[1] Mayo Clin Rochester, Div Med Oncol, 200 First St SW, Rochester, MN 55905 USA
[2] Dept Immunol, 200 First St SW, Rochester, MN 55905 USA
[3] Div Oncol Res, 200 First St SW, Rochester, MN 55905 USA
[4] Dept Biostat & Informat, 200 First St SW, Rochester, MN 55905 USA
[5] Mayo Clin Jacksonville, Dept Hematol Oncol, 4500 San Pablo Rd, Jacksonville, FL 32224 USA
[6] Immune Design Inc, 1616 Eastlake Ave E 310, Seattle, WA 98102 USA
关键词
glucopyranosyl lipid A; immunotherapy; MART-1; melanoma; peptide; Phase I; T cell; vaccine; T-CELLS; GLA-SE; ADJUVANT; RESPONSES; INTERLEUKIN-2; EXPRESSION; MULTIPLE; TRIAL;
D O I
10.2217/imt-2020-0085
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim:We tested the safety and immunogenicity of a novel vaccine in patients with resected high-risk melanoma.Patients & methods:HLA-A2-positive patients with resected Stage II-IV melanoma were randomized to receive up to three vaccinations of melanoma-associated peptide (MART-1a) combined with a stable oil-in-water emulsion (SE) either with the Toll-like receptor 4 agonist glucopyranosyl lipid A (GLA-SE-Schedule 1) or alone (SE-Schedule 2). Safety and immunogenicity of the vaccines were monitored.Results: A total of 23 patients were registered. No treatment-related grade 3 or higher adverse events were observed. Increases in MART-1a-specific T cells were seen in 70 and 63% of Schedule 1 and Schedule 2 patients, respectively.Conclusion:Both vaccine schedules were well-tolerated and resulted in an increase in MART-1a-specific T cells.
引用
收藏
页码:983 / 995
页数:13
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