Research Areas
- Cancer immunology
- Human papillomavirus-induced cancers
- Microbiome and host interactions
- Immune and microbial biomarkers for cancer treatment responses
Scientific Achievements
- Identified immune and microbial cells relevant for oropharyngeal and cervical cancer development and cancer treatment responses.
- Results from our studies could be used to better identify patients who would benefit from specific cancer therapies.
- 12 publications since the RCMI Pilot Project award in the areas of cancer and infectious diseases.
- 18 students trained.
- Díaz-Rivera et al. (2024). Cancers, 16(11), 2065. PMID: 38893183
- Galán-Ortíz et al. (2023). B cells modulate HPV+ oropharyngeal cancer in a preclinical model. Front Oncol, PMID: 37035195
Funding
RCMI Funding:
- NIH/NIMHD U54MD007600: Pilot Project “Characterization of B cells involved in anti-PD-1 resistance in HPV+ oral tumors”
Other funding obtained with RCMI support: R16DE035974 (NIH/NIDCR 2025 – 2029); 1P20GM157613-01 (NIH/NIGMS RPL 2025 – 2028)
Scientific Advance
Immune and Microbial Signatures Associated with PD-1 Blockade Sensitivity in a Preclinical Model for HPV+ Oropharyngeal Cancer
Published in Cancers, Volume 11, 2024, PMCID: PMC11171047.
Published in Cancers, Volume 11, 2024, PMCID: PMC11171047.
In this study, the researchers used a mouse model of HPV-positive oropharyngeal cancer to examine how response to anti-PD-1 immunotherapy relates to both immune cell profiles and the composition of the oral microbiome. They found that in treatment responders, there were higher numbers of activated immune cells — including specific T cell, B cell, dendritic cell and myeloid cell populations — in tumors, tumor-draining lymph nodes, and blood. Moreover, certain bacterial types in the oral cavity (like Allobaculum, Blautia, Faecalibacterium, Dorea, and Roseburia) were more abundant in responders, while non-responders had more Enterococcus. These immune and microbial patterns may serve as biomarkers to predict which HPV-positive oropharyngeal cancer patients will benefit from PD-1 blockade therapies.
U54 MD007600/MD/NIMHD NIH HHS/United States, P20 GM103475/GM/NIGMS NIH HHS/United States, U54 GM133807/GM/NIGMS NIH HHS/United States, R25GM061838/RISE Research Initiative for Scientific Enhancement award, U54 CA096297/CA/NCI NIH HHS/United States
