Study finds 'supercharging' T cells with mitochondria enhances their antitumor activity

Investigators from Brigham and Women's Hospital, a founding member of the Mass General Brigham healthcare system, in collaboration with colleagues at Leibniz Institute for Immunotherapy in Germany, have developed a way to "supercharge" T cells by supplying them with extra mitochondria from multipotent stromal cells. In a new study published in Cell, researchers report that these supercharged T cells exhibited heightened anti-tumor activity and reduced signs of exhaustion in preclinical models of cancer, suggesting that this technique could help improve existing immunotherapies.

"These supercharged T cells overcome one of the fundamental barriers of immunotherapy by penetrating the tumor and overcoming immune barren state in the tumor," said corresponding author Shiladitya Sengupta, PhD, of the Brigham's Department of Medicine. "Mitochondria provide the fuel. It's like we're taking T cells to the fuel station and gassing them up. This transplanting of mitochondria is the dawn of organellar therapywhere an organelle is delivered to a cell to make it more effective."

"Previous efforts to enhance mitochondrial function in T cells have focused on targeting specific genes or pathways, but these methods fall short when the mitochondria are already damaged or dysfunctional. Our approach involves the transfer of whole, healthy mitochondria organelles into the cells. This process is comparable to organ transplantation -- like heart, liver, or kidney transplants -- but conducted at a microscopic level," explained Luca Gattinoni, MD, co-leading author of the study.

To develop this method, the researchers built upon their previous findings, which showed that cancer cells can slurp up mitochondria from immune cells through intercellular nanotubes that the researchers have described as "tiny tentacles." Drawing from these results, the group teamed up with scientists at the Leibniz Institute to investigate interactions between bone marrow stromal cells (BMSCs) and cytotoxic T cells. Using varied electron and fluorescent microscopy approaches, they observed that BMSCs extended nanotubes to activated T cells, donating intact mitochondria. This helped to revive the T cells (mito⁺), which showed increased respiratory capacity, a sign of enhanced metabolism.

The research team examined how supercharging the T cells affected immune function. When infused into a mouse model of melanoma, mito⁺ cells showed significantly higher anti-tumor responses and prolonged survival rates compared to T cells without additional mitochondria. Further experiments revealed that mito⁺ cells could easily penetrate tumors, multiply quickly and pass on their extra mitochondria to daughter cells, where they persisted for a long time. In addition, the authors discovered that mito⁺ cells could survive and resist T cell exhaustion within the tumor microenvironment.

The researchers found that supercharging human T cells helped the immune system fight tumors in multiple models of cancer. Of note, they demonstrated that tumor-infiltrating lymphocytes and CAR-Ts, which often develop damaged mitochondria within the tumor microenvironment, displayed augmented cancer-destroying properties when boosted with mitochondria from primary BMSCs from human donors.

The authors suggest that future applications could include using patient-matched BMSCs to supercharge T cells for adoptive transfer.