One Cell Type May Quash Tumor Vaccines
A single cell type could explain why cancer vaccines have a tough time stimulating the immune system to fight tumors.
(PHILADELPHIA) -- Most cancer vaccines have not lived up to their promise in clinical trials. The reason, many researchers suspect, is that the immune cells that would help the body destroy the tumor – even those reactions boosted by cancer vaccines – are actively suppressed. Now, researchers at Thomas Jefferson University have found that a single cell type is actively suppressed in several experimental cancer vaccines, paving the way toward methods to break suppression and improve the effectiveness of cancer vaccines. The work was published online in the European Journal of Immunology.
“The conventional wisdom is that the body knocks out all of the cells that can mount an immune response to the cancer,” says first author Adam Snook, PhD, a Research Instructor at Thomas Jefferson University. “In fact, our work shows that it’s only one cell type that is affected. But that cell, the T-helper cell, acts as the lynchpin.”
Cancer vaccines are designed to boost the body’s natural defenses against cancer. They work by training the immune system to recognize and attack specific tumor peptides, which are a kind of identification tag for tumors. These peptide “tags” help the immune system find and attack cancer cells. There are three types of cells that can “see” and react to these tags: T-helper cells, cytotoxic T cells, and B cells, and researchers thought that all three were trained, or tolerized, to ignore the tags on cancer cells.
Dr. Snook and colleagues tested which cell was involved by inoculating mice with a cancer vaccine they developed for colorectal cancer using a tumor peptide called guanylyl cyclase C (GUCY2C). Normally, GUCY2C-vaccinated mice would not produce much of an immune response, from either T cell type or B cells. However, when the researchers boosted the GUCY2C vaccine by linking it to another peptide called S1 that efficiently activates T-helper cells, they were able to see a vigorous activation of cytotoxic T cells and B cells directed at GUCY2C.
In fact, the GUCY2C vaccine-S1 combo improved the survival time of mice with cancer by months compared to only days with GUCY2C vaccine alone. In fact, many mice were cured of their disease.
When Dr. Snook tested two other cancer peptides, one for breast cancer (Her2) and one for melanoma (Trp2), he saw similar results, suggesting that selective inactivation of T helper cells occurs for peptides found in many cancer types. “The results make a lot of sense,” says Dr. Snook. “T-helper cells, as their name suggests, provide help to both cytotoxic T cells and to B cells. The entire peptide-specific immune response can be taken out by tolerizing this one cell type.”
In addition, T-helper cells are also essential for creating immunological memory. Boosting T-helper cell activation also protected mice from challenge with cancer months after the initial vaccination, increasing their survival and decreasing tumor number.
The next step is to test whether a T helper peptide-linked GUCY2C vaccine could help fight colorectal cancer in humans. Dr. Snook and colleagues are currently enrolling patients in a clinical trial aimed at reducing the rate of cancer recurrence in patients who had their primary tumors removed.
The work was funded by NIH (R01 CA75123, R01 CA95026, RC1 CA146033, P30 CA56036, R01 CA170533; F31 CA171672); Targeted Diagnostic and Therapeutics Inc.; and a Measey Foundation Fellowship. Scott Waldman is the Samuel M.V. Hamilton Professor of Thomas Jefferson University. This project was funded, in part, by grants from the Pennsylvania Department of Health (SAP #4100059197, SAP #4100051723). The Department specifically disclaims responsibility for any analyses, interpretations or conclusions. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Scott Waldman was the Chair of the Data Safety Monitoring Board for the C-Cure Trialä sponsored by Cardio Biosciences, and the Chair (uncompensated) of the Scientific Advisory Board to Targeted Diagnostics and Therapeutics, Inc. which provided research funding that, in part, supported this work and has a license to commercialize inventions related to this work. All other authors declare no financial or commercial conflict of interest.
For more information, contact Edyta Zielinska, (215) 955-5291, Edyta.Zielinska@jefferson.edu.
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Thomas Jefferson University (TJU), the largest freestanding academic medical center in Philadelphia, is nationally renowned for medical and health sciences education and innovative research. Founded in 1824, TJU includes Jefferson Medical College (JMC), one of the largest private medical schools in the country and ranked among the nation’s best medical schools by U.S. News & World Report, and the Jefferson Schools of Nursing, Pharmacy, Health Professions, Population Health and the Graduate School of Biomedical Sciences. Jefferson University Physicians is TJU’s multi-specialty physician practice consisting of the full-time faculty of JMC. Thomas Jefferson University partners with its clinical affiliate, Thomas Jefferson University Hospitals.
Article Reference: AE Snook, et al., “Self-tolerance eliminates CD4+ T, but not CD8+ T or B, cells corrupting cancer immunotherapy,” European Journal of Immunology, DOI: 10.1002/eji.201444539, 2014.