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The combination of GM-CSF and IL-2 as local adjuvant shows synergy in enhancing peptide vaccines and provides long term tumor protection

  • Antoun Toubaji
    ,
  • Sarah Hill
    ,
  • Masaki Terabe
    ,
  • Jiahua Qian
    ,
  • Tamara Floyd
    ,
  • R. Mark Simpson
*Corresponding author for this work
  • National Institutes of Health
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Many strategies have been used to enhance the peptide vaccine immune response and to establish therapeutic benefits. This includes the utilization of cytokines to improve antigen presentation or enhance T cell response. Here, we have tested the combination of GM-CSF and IL-2 as locally administered adjuvant to enhance the immune response to the HPV16 E7 peptide. Female C57BL/6 mice were immunized intradermally with a 9-mer HPV16 E7 peptide (aa: 49-57) alone, or in combination with GM-CSF, IL-2, or both cytokines. Specific immune responses were measured by ELISA and Chromium-Release Assays. Furthermore, therapeutic effects of these vaccines and long term tumor protection were assessed in mice bearing established tumors. We showed that GM-CSF and IL-2, when co-administered locally in an emulsion with peptide, exert a synergistic effect in enhancing the immune response to the antigen. This combination induced higher CTL and cytokine release responses and did not increase the Treg population. Therapeutic intervention with this synergistic combination led to a complete response of established tumors. Furthermore, this combination induced a memory response which protected mice against subsequent additional tumor challenge. We identified a new vaccine adjuvant, a local combination of GM-CSF and IL-2, which is synergistic in enhancing peptide specific immune response through local effect without increasing Treg cells. This immune response was found to be long lasting and protective in tumor bearing mice.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 5882-5891 (10 pages)

Journal (Volume, Issue Number)

Vaccine (Volume 25, Issue 31)

Publication milestones

  • Published - 08/01/2007

Publication status

Published - 08/01/2007

ISSN

0264-410X

Publication IDs

  • Scopus: 34447272278
  • PubMed: 17602804

Publication metrics

Metrics

SciVal
FWCI
1.23
SciVal
Author count
8
SciVal
citations
39
SciVal
Paper percentile
85
Scopus
citations
Fractional count
1
Fractional count
0.13
Fractional count
7
Fractional count
0.88
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
22
Citation count
47

Funding Details

This research was supported by the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research.
FundersFunding number
Center for Cancer Research
-
NIH
-
NCI
Z01SC004020