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News — New York, NY—October 12, 2023—For several years, researchers have been successfully using chimeric antigen receptor (CAR) T cells to target specific antigens found on blood cells as a cure for patients with leukemia and lymphoma. But solid tumors, like breast and colon cancers, have proven to be more difficult to home in on. Solid tumors contain a mix of cells that display different antigens on their surface-often shared with healthy cells in the body. Thus, identifying a consistent and safe target has impeded the success of most CAR-T cell therapy for solid tumors at the first phase of development.

Breakthrough approach to fighting cancer

Synthetic biologists at report today a new approach to attacking tumors. They have engineered tumor-colonizing bacteria (probiotics) to produce synthetic targets in tumors that direct CAR-T cells to destroy the newly highlighted cancer cells.   

“Our probiotic platform enables CAR-T cells to attack a broad range of tumor types,” said , associate professor of, who led the  by . “Traditional CAR-T therapies have relied on targeting natural tumor antigens. This is the first example of pairing engineered T cells with engineered bacteria to deliver synthetic antigens safely, systemically, and effectively to solid tumors. This could have a significant impact on the treatment of many cancers.”

Painting targets on solid tumors

 has essentially created a universal CAR-T cell that attacks a universal antigen, by programming the tumor-seeking bacteria to paint solid tumors with a synthetic marker that the CAR-T cells can recognize. The researchers expect that, with further refinements, this platform will enable the treatment of any solid tumor type without the need to identify a specific tumor antigen -  thus bypassing the need to generate a custom CAR-T cell product for each cancer type and each patient. 

Engineering “living medicines”

This probiotic-guided CAR-T cell (ProCAR) platform is the first time that scientists have not only successfully combined engineered probiotics with CAR-T cells, but have also demonstrated the first evidence of CARs responding to synthetic antigens produced directly within the tumor.  

“Combining the advantages of tumor-homing bacteria and CAR-T cells provides a new strategy for tumor recognition, and this builds the foundation for engineered communities of living therapies,” said the study’s co-lead author Rosa Vincent, a PhD student working in Danino’s lab. “We chose to bridge the individual limitations of these two cell therapies by combining the best features of each – using bacteria to place the targets, and T cells to destroy the malignant cells.”

Safe and effective platform

The platform has proven to be safe and effective across multiple models of human and mouse cancers in both immunocompromised and immune-healthy mice. In fact, the study shows that human T cells in particular benefit so much from the presence of immunostimulatory bacteria within the tumor that their tumor-killing functions are further enhanced.

“Overall, our ProCAR platform represents a new strategy for enhancing the effectiveness of CAR-T cell therapy in solid tumors,” said Danino, who is also affiliated with the  and . “While we’re still in the research phase, it could open up new avenues for cancer therapy.” 

Next steps in an ongoing collaboration

This work was done as part of an ongoing collaboration with the laboratory of , assistant professor of microbiology and immunology at Columbia’s Vagelos College of Physicians and Surgeons. The team has  bacteria that deliver immunotherapy payloads together. The researchers are continuing to refine their work and hope to begin clinical trials to fully assess the platform’s safety and efficacy in human patients.   

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About the Study

Journal: Science

The study is titled “.”

Authors are: Rosa L. Vincent¹, Candice R. Gurbatri¹, Fangda Li², Ana Vardoshvili¹, Courtney Coker¹, Jongwon Im¹, Edward R. Ballister^1,2, Mathieu Rouanne², Thomas Savage², Kenia de los Santos-Alexis², Andrew Redenti^1,2, Leonie Brockmann², Meghna Komaranchath¹, Nicholas Arpaia^2,3, Tal Danino^1,3,4

¹Department of Biomedical Engineering, Columbia Engineering

²Department of Microbiology & Immunology, Vagelos College of Physicians and Surgeons of Columbia University

³Herbert Irving Comprehensive Cancer Center, Columbia University

⁴Data Science Institute, Columbia University

This work was supported by NIH 1R01EB030352, Columbia Translational Therapeutics (TRx) Award, and the NSF Graduate Research Fellowship (1644869 to C.R.G.).

R.L.V., T.M.S., C.R.G., J.I., N.A., and T.D. are inventors on a patent application describing the use of Probiotic-guided CAR-T cells for cancer immunotherapy (International Application No. PCT/US2022/016775). 

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LINKS:

Paper:

DOI:  10.1126/science.add7034