New Antibody Therapy 77A Shows Promise Against Blood Cancers

Researchers from The University of Texas MD Anderson Cancer Center have developed an investigational antibody therapy known as 77A, which demonstrates potential in enhancing immune responses against both blood cancers and solid tumors. This innovative therapy was presented at the 67th American Society of Hematology (ASH) Annual Meeting in Orlando on December 6, 2025, highlighting its ability to combat treatment resistance in conditions like myeloma and lymphoma.

The study, spearheaded by Jun Wei, M.D., Ph.D., an assistant professor in the Department of Lymphoma & Myeloma, alongside principal investigator Robert Z. Orlowski, M.D., Ph.D., also from the same department, reveals that 77A works by targeting a cancer survival protein known as HSP70. This protein is often overexpressed in tumors, helping them evade immune responses and contribute to an environment that supports cancer cell survival.

Mechanism and Effectiveness of 77A

The mechanism behind 77A is intriguing. By targeting HSP70, the antibody activates T cells and natural killer (NK) cells, reshaping the tumor environment and fostering long-lasting immune responses. In laboratory models, 77A not only displayed strong antitumor effects but also enhanced the efficacy of existing treatments, including chemotherapy, radiation therapy, and immunotherapies like immune checkpoint blockade. Furthermore, it exhibited potential compatibility with adoptive T cell therapy, a cutting-edge method wherein patients receive lab-grown immune cells designed to attack cancer cells.

“We see tremendous promise in how 77A can rewire the immune system, enabling effective responses against multiple cancers,” Wei stated. The findings indicate that this therapy may pave the way for new pathways in immunotherapy, potentially transforming patient treatment approaches.

Future Directions and Clinical Trials

The implications of this research extend beyond laboratory settings. Early experiments with human immune cells suggest that 77A could also enhance immune responses in healthy donors, indicating a broader therapeutic potential. This positions 77A as a promising candidate for future clinical trials, which aim to evaluate its efficacy across various cancer types.

Orlowski expressed optimism about the future of 77A, stating, “These results give us confidence that 77A could become a versatile immunotherapy. Our next step is to advance a humanized version of this antibody into clinical trials to evaluate its potential in patients across multiple cancer types.”

The development of the humanized version of 77A is currently underway, with plans to initiate clinical trials soon. This research is supported by Blood Cancer United, formerly known as the Leukemia & Lymphoma Society, which emphasizes the collaborative effort in advancing cancer treatment.

As the medical community continues to explore innovative therapies, the findings presented by MD Anderson offer hope for improved treatment options for patients facing challenging diagnoses in both blood and solid cancers.