Scientific article

Short Peptide Vaccine Induces CD4+ T Helper Cells in Patients with Different Solid Cancers

Published inCancer immunology research, vol. 4, no. 1, p. 18-25
Publication date2016-01-01
First online date2016-01-03

Previous cancer vaccination trials often aimed to activate CD8+ cytotoxic T-cell (CTL) responses with short (8–10mer) peptides and targeted CD4+ helper T cells (TH) with HLA class II–binding longer peptides (12–16 mer) that were derived from tumor antigens. Accordingly, a study of immunomonitoring focused on the detection of CTL responses to the short, and TH responses to the long, peptides. The possible induction of concurrent TH responses to short peptides was widely neglected. In a recent phase I vaccination trial, 53 patients with different solid cancers were vaccinated with EMD640744, a cocktail of five survivin-derived short (9- or 10-mer) peptides in Montanide ISA 51VG. We monitored 49 patients and found strong CD8+ T-cell responses in 63% of the patients. In addition, we unexpectedly found CD4+ TH cell responses against at least two of the five short peptides in 61% (23/38) of the patients analyzed. The two peptides were recognized by HLA-DP4– and HLA-DR–restricted TH1 cells. Some short peptide–reactive (sp)CD4 T cells showed high functional avidity. Here, we show that a short peptide vaccine is able to activate a specific CD4+ T-cell repertoire in many patients, facilitating a strong combined CD4+/CD8+ T-cell response. Cancer Immunol Res; 4(1); 18–25. ©2015 AACR.

Citation (ISO format)
GROSS, Stefanie et al. Short Peptide Vaccine Induces CD4+ T Helper Cells in Patients with Different Solid Cancers. In: Cancer immunology research, 2016, vol. 4, n° 1, p. 18–25. doi: 10.1158/2326-6066.CIR-15-0105
Main files (1)
Article (Published version)
ISSN of the journal2326-6066

Technical informations

Creation12/06/2023 3:21:04 PM
First validation03/20/2024 10:28:01 AM
Update time03/20/2024 10:28:01 AM
Status update03/20/2024 10:28:01 AM
Last indexation03/20/2024 10:28:21 AM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack