NIH-funded research R01 grant

How HPV-targeting immune cells affect immunotherapy responses in HPV-positive head and neck cancer

Official title: Mechanistic connection between HPV-specific TCRs and therapeutic responses to ICI in HPV+ HNSCC

Funded at University of Pittsburgh at Pittsburgh · NIH-11306668 · Data updated 2026-11-12

This project looks at whether specific HPV-targeting T cells help people with HPV-positive head and neck cancer respond better to immune checkpoint drugs.

More HNSCC research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Pittsburgh at Pittsburgh
NIH-funded
Lab location1 site (Pittsburgh, United States)
Project startApril 1, 2024
Project endMarch 31, 2029
Funding year2026
Award (this year)$655,244
NIH project number5R01CA282074-03
Project IDNIH-11306668 on NIH RePORTER

Who could benefit from this research

Could help

Adults with HPV-positive head and neck squamous cell carcinoma, especially those treated with or being considered for immune checkpoint inhibitors or willing to provide tumor or blood samples, are the ideal candidates.

Less likely to help

People with HPV-negative head and neck cancer or those not eligible for immunotherapy or unable to provide tissue or blood samples are unlikely to be included or benefit directly.

What this research studies

You would be asked to let researchers study tumor and blood samples from people with HPV-positive head and neck cancer who received immune checkpoint therapy. The team will map T cell receptors (TCRs) that recognize different HPV proteins (for example E2, E6, and E7) and compare the breadth and depth of those responses with patients' treatment outcomes. They will also test selected TCRs in mouse models to see which HPV-directed T cells control tumors or work together with checkpoint drugs. Combining human clinical samples and laboratory models aims to reveal which HPV-specific immune responses help or limit immunotherapy.

Why it matters

Potential benefit: If successful, this work could help predict who will benefit from checkpoint inhibitors and guide development of HPV-targeted T-cell therapies.

How similar studies have gone: Previous clinical and laboratory work shows HPV-positive tumors can respond well to anti-PD1 and that HPV-specific T-cell approaches (mostly targeting E7) have promise, but directly linking specific HPV-TCR patterns—including E2 responses—to immunotherapy outcomes is a newer, mechanistic question.

Where this research is happening

  • University of Pittsburgh at Pittsburgh
    Pittsburgh, United States
    Active

Researchers

  • Principal investigator: Wang, Jing Hong — University of Pittsburgh at Pittsburgh
  • Study coordinator: Wang, Jing Hong

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.