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.

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.

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