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Circulating regulatory T cells (CD4+CD25+FOXP3+) decrease in breast cancer patients after vaccination with a modified
Jeremy D Gates1, Guy T Clifton, Linda C Benavides
1Department of Surgery, General Surgery Service, Brooke Army Medical Center, Ft. Sam Houston, TX 78234, USA.
Vaccine
|September 23, 2010
Summary
Regulatory T cells (T(Reg)) decreased in breast cancer patients vaccinated with AE37, correlating with enhanced immune responses. This suggests the AE37 vaccine may be clinically useful for cancer immunotherapy.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Regulatory T cells (T(Reg)), characterized as CD4(+)CD25(+)FOXP3(+), play a crucial role in immune suppression within the tumor microenvironment.
- Understanding T(Reg) cell dynamics is vital for developing effective cancer immunotherapies.
Purpose of the Study:
- To analyze the impact of the modified HLA class II HER2/neu peptide (AE37) vaccine on T(Reg) cell populations in breast cancer patients.
- To correlate changes in T(Reg) cell levels with vaccine-specific immune responses.
Main Methods:
- Peripheral blood lymphocytes (PBL) from breast cancer patients were analyzed for T(Reg) cell counts.
- Immune responses were assessed using IFN-γ ELISPOT and dermal delayed-type hypersensitivity (DTH) tests.
- Correlations between T(Reg) cell levels and immune responses were evaluated.
Main Results:
- A significant decrease in mean CD4(+)CD25(+)FOXP3(+) T(Reg) cells was observed post-vaccination.
- No significant changes were noted in serum TGF-β levels.
- IFN-γ ELISPOT and DTH responses increased after AE37 vaccination.
- A strong correlation was found between T(Reg) cell reduction and the size of DTH to AE37.
Conclusions:
- The AE37 vaccine effectively reduces T(Reg) cells in breast cancer patients.
- The observed reduction in T(Reg) cells is associated with enhanced vaccine-specific immune responses, including DTH.
- These findings suggest the AE37 vaccine holds potential clinical utility in cancer immunotherapy.
