Related Experiment Video
Updated: Aug 6, 2026

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
New Therapeutic Cancer Vaccine with Lenalidomide Induces Potent T Cell Immunity and Inhibits HPV E6/E7-Expressing
Yohannes Gemechu1, Sonia Mukherjee2, Jeffrey A Gelfand1
1Massachusetts General Hospital and Harvard Medical School Boston, MA United States.
Abstract:
Current prophylactic human papillomavirus (HPV) vaccines prevent infection but have limited therapeutic benefit in established HPV-driven malignancies. To address this unmet need, we developed VTX-067, a modular self-assembling therapeutic cancer vaccine consisting of a recombinant Mycobacterium tuberculosis heat shock protein 70-avidin fusion (MAV) noncovalently bound to biotinylated HPV E6/E7 MHC class I- and II-restricted peptide concatemers. MAV is produced in CHO cells with minimal endotoxin. Assembled VTX-067 is designed to elicit both CD4⁺ and CD8⁺ T-cell responses against HPV-associated tumors. In multiple tumor models expressing HPV E6/E7, intradermal vaccination with VTX-067 induced potent and dose-dependent HPV E6/E7-specific CD8⁺ and CD4⁺ T-cell responses without evidence of local reactogenicity. Therapeutic vaccination significantly delayed subcutaneous tumor progression, extended survival, and provided durable protection against tumor rechallenge. VTX-067 treatment increased intratumoral CD8⁺ T-cell infiltration, elevated the CD8:Treg ratio, and upregulated a Th1/cytotoxic transcriptional program including Ifnγ, Tbx21, Stat1, and Gzmb. Depletion of CD8⁺ T cells eliminated vaccine efficacy, while adoptive transfer of VTX-067-primed CD8⁺ T cells conferred tumor protection in recipient mice. In a cervicovaginal orthotopic model, both intradermal and intramucosal administration generated systemic E6/E7-specific effector responses and sustained control of mucosal tumors. Notably, combining a suboptimal VTX-067 dose with the immunomodulatory agent lenalidomide further enhanced tumor control and survival, demonstrating a potential dose-sparing strategy. These findings establish VTX-067 as a safe, highly immunogenic therapeutic vaccine with CD8⁺ T-cell-dependent antitumor activity, and support its clinical development alone or in combination with immune-modulating agents for HPV-associated cancers.
Insights
A new therapeutic cancer vaccine, VTX-067, shows promise for treating human papillomavirus (HPV)-driven cancers by eliciting robust T-cell responses. This vaccine demonstrated significant antitumor activity and durable protection in preclinical models, supporting clinical development.
Area of Science:
- Oncology
- Immunology
- Vaccinology
Background:
- Current prophylactic human papillomavirus (HPV) vaccines are effective against infection but lack therapeutic benefit for established HPV-driven malignancies.
- There is a critical unmet need for effective treatments for patients with existing HPV-associated cancers.
Purpose of the Study:
- To develop and evaluate VTX-067, a novel modular self-assembling therapeutic cancer vaccine, for its potential to treat HPV-driven tumors.
- To assess the immunogenicity, safety, and therapeutic efficacy of VTX-067 in preclinical models of HPV-associated cancers.
Main Methods:
- VTX-067 was constructed using a recombinant Mycobacterium tuberculosis heat shock protein 70-avidin fusion (MAV) bound to biotinylated HPV E6/E7 peptide concatemers.
- The vaccine's ability to elicit CD4+ and CD8+ T-cell responses, antitumor activity, and safety profile were evaluated in multiple HPV E6/E7-expressing tumor models.
- Immunological assessments included measuring T-cell infiltration, cytokine profiles, and the impact of T-cell depletion and adoptive transfer.
Main Results:
- VTX-067 vaccination induced potent, dose-dependent HPV E6/E7-specific CD8+ and CD4+ T-cell responses without local reactogenicity.
- Therapeutic vaccination significantly delayed tumor progression, extended survival, and provided durable protection against tumor rechallenge in preclinical models.
- VTX-067 increased intratumoral CD8+ T-cell infiltration, enhanced the CD8:Treg ratio, and promoted a Th1/cytotoxic transcriptional program. Combination with lenalidomide showed enhanced efficacy.
Conclusions:
- VTX-067 is a safe and highly immunogenic therapeutic cancer vaccine with significant CD8+ T-cell-dependent antitumor activity against HPV-associated malignancies.
- The findings support the clinical development of VTX-067 as a monotherapy or in combination with immune-modulating agents for HPV-associated cancers.
More Related Videos
Related Concept Videos
Tumor Immunotherapy
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...

