Northwestern reengineers HPV vaccine to boost T cell attack on tumors

Researchers at Northwestern University have developed a more effective therapeutic vaccine for HPV-related cancers by rearranging components in a DNA-based nanoparticle. This structural adjustment significantly enhances the immune system's ability to target and destroy tumors. The findings, published in Science Advances, highlight the importance of molecular arrangement in vaccine design.

Scientists at Northwestern University have demonstrated that the physical arrangement of components in a cancer vaccine can greatly influence its effectiveness. In a study published on February 11 in Science Advances, the team focused on therapeutic vaccines for cancers driven by the human papillomavirus (HPV), which causes most cervical cancers and an increasing share of head and neck cancers.

The vaccine is based on spherical nucleic acids (SNAs), a nanotechnology invented by Chad A. Mirkin, the George B. Rathmann Professor at Northwestern. Unlike traditional vaccines that mix antigens and adjuvants without precise structure—a method Mirkin calls the 'blender approach'—this design organizes elements at the nanoscale. The researchers tested variations where a fragment of an HPV protein, known as an antigen, was positioned differently within the SNA nanoparticle.

Three configurations were evaluated in humanized mouse models of HPV-positive cancer and in tumor samples from head and neck cancer patients. The most effective version displayed the antigen on the nanoparticle's surface, attached via its N-terminus. This led to up to eight times more interferon-gamma production by CD8 T cells, the immune system's key cancer fighters. In animal models, it slowed tumor growth and extended survival. In patient samples, it increased cancer cell killing by twofold to threefold.

'This effect did not come from adding new ingredients or increasing the dose,' said Dr. Jochen Lorch, a professor of medicine at Northwestern and medical oncology director for the Head and Neck Cancer Program. 'It came from presenting the same components in a smarter way. The immune system is sensitive to the geometry of molecules.'

The study underscores the emerging field of structural nanomedicine, which Mirkin pioneered. 'The promise of structural nanomedicine is being able to identify from the myriad possibilities the configurations that lead to the greatest efficacy and least toxicity,' Mirkin stated. 'In other words, we can build better medicines from the bottom up.'

Previous SNA-based vaccines have targeted melanoma, triple-negative breast cancer, colon cancer, prostate cancer, and Merkel cell carcinoma, with seven advancing to human trials. The team plans to apply these insights to refine earlier candidates and incorporate artificial intelligence to optimize designs. The research was supported by the National Cancer Institute and the Robert H. Lurie Comprehensive Cancer Center at Northwestern University.

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Scientific illustration depicting nasal nanodrops activating immune cells to eliminate glioblastoma tumors in a mouse model.
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Nasal nanodrops wipe out glioblastoma tumors in mice

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Researchers at Washington University School of Medicine in St. Louis, working with scientists at Northwestern University, have developed a noninvasive nasal nanotherapy that activates the immune system to attack aggressive brain tumors in mice. By delivering spherical nucleic acids that trigger the STING immune pathway directly from the nose to the brain, the approach eliminated glioblastoma tumors in mouse models when combined with drugs that boost T-cell activity, according to a study in the Proceedings of the National Academy of Sciences.

A Northwestern University team reports that redesigning the chemotherapy drug 5‑fluorouracil as a spherical nucleic acid markedly increased its cancer‑cell uptake and efficacy in acute myeloid leukemia models, with no observable side effects, according to a study published October 29 in ACS Nano.

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Scientists have created innovative nanoparticles designed to destroy harmful proteins linked to dementia and cancer. These particles can access difficult tissues like the brain and precisely eliminate problematic proteins without broad side effects. The technology shows early promise for precision medicine.

Scientists at Washington State University used artificial intelligence and molecular simulations to identify a crucial amino acid interaction in a herpes virus fusion protein that is required for cell invasion. When they engineered a mutation at this site, the virus could no longer fuse with or enter cells, according to a study published in Nanoscale.

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Researchers at Cold Spring Harbor Laboratory have identified key proteins and protein complexes that help certain carcinomas shift their cellular identity and potentially evade treatment. Two new studies, focusing on pancreatic cancer and tuft cell lung cancer, highlight molecular structures that could become targets for more precise and selective therapies.

Scientists have developed an ultra-sensitive Raman imaging system that identifies cancerous tissue by detecting faint light signals from nanoparticles bound to tumor markers. This technology, far more sensitive than current tools, could accelerate cancer screening and enable earlier detection. Led by researchers at Michigan State University, the system promises to bring advanced imaging into clinical practice.

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Scientists have developed a light-based sensor that can identify tiny amounts of cancer biomarkers in blood samples, potentially enabling earlier detection than traditional scans. The technology combines DNA nanostructures, CRISPR, and quantum dots to produce a clear signal from just a few molecules. Tests on lung cancer patient serum showed promising results at sub-attomolar levels.

 

 

 

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