Researchers Develop New One-Two Punch Against Melanoma in Mouse Model
Posted by: Crystal Williams on: February 21, 2019 | Print This Page
Updated, safer versions of diphtheria fusion toxin DAB-IL-2 show promise in reducing tumor growth
Researchers at the Bloomberg~Kimmel Institute for Cancer Immunotherapy at Johns Hopkins and the Johns Hopkins University School of Medicine report two new forms of an older anti-cancer agent they developed appear to enhance the immune system’s ability to fight melanoma in mice.
The agents, dubbed s-DAB-IL-2 and s-DAB-IL-2(V6A), comprise a regulatory protein called human interleukin-2 fused to chemically modified portions of diphtheria toxin.
In a mouse model of melanoma, the two agents, when given together, depleted so-called T regulatory cells that infiltrate tumors and hinder the immune system’s ability to fight cancer, according to the researchers, whose published report on the experiments appears in the February issue of Proceedings of the National Academy of Sciences.
The investigators said each of the compounds individually depleted the regulatory cells in the mice, but increased the depletion rate when used before an immunotherapy treatment known as checkpoint blockade, providing a one-two punch against cancer.
“Our study demonstrates that these proteins show good potential as an immunotherapy option,” says senior study author William Bishai, M.D., Ph.D., professor of medicine. “When paired with checkpoint inhibitor therapy, they allow the immune system to develop a much more robust one-two punch anti-tumor response, leading to an almost complete knockout of tumor.”
Bishai says more animal research, along with safety and effectiveness studies in humans, must be done before the proteins can be prescribed for people with melanoma, a skin cancer that although relatively rare, kills about 7,300 Americans each year.
The novel proteins used in the mouse experiments are re-engineered forms of denileukin diftitox (DAB-IL-2), a diphtheria
Many T cell lymphomas have a high density of the IL2 receptor (CD25). The targeted toxin therapies bind to the IL2 receptor, and then the diphtheria toxin portion of the molecule delivers a lethal enzyme to the targeted cell which results in cell death within hours. (Credit: Johns Hopkins Kimmel Cancer Center)
toxin-based fusion protein that was approved by the U.S. Food and Drug Administration in 1999 and marketed under the name Ontak for the treatment of persistent or recurrent cutaneous T-cell lymphoma, a cancer of the immune system. Ontak was prescribed for 11 years for other conditions as well, including peripheral T-cell lymphoma, graft versus host disease and psoriasis. Then, in 2011, the FDA put the drug on clinical hold, in part because up to 25 percent of patients who received it developed vascular leak syndrome, a condition marked by fluid retention, or lung or heart failure.
Ontak was developed by study co-author John “Jack” Murphy, Ph.D., professor of medicine at Johns Hopkins, when he worked at Harvard Medical School. Bishai was one of his graduate students in the 1980s.
DAB-IL-2 sprouted from an interest in diphtheria toxin, which was long recognized as a potent biological poison, Murphy says. He worked for years to engineer a form of the toxin that would attach only to cells that had specific receptors they wanted to target.
One study Murphy and Bishai worked on, published in 1986, targeted the biologic activity of diphtheria toxin specifically to melanoma cells.
“That was the first indication that we could deliberately change the target cell specificity of DT from a generalized poison to a poison that would only go to cells we wanted to eliminate,” says Murphy.
At the time it was put on hold, DAB-IL-2 was considered a potential immunotherapy to deplete T regulatory cells in patients with advanced, malignant melanoma that could no longer be treated with surgery. Phase 2 clinical studies demonstrated it was at least as effective in stopping tumor progression or possibly more effective than checkpoint inhibitors alone, Murphy says.
Murphy came to Johns Hopkins in 2015 to work with Bishai again, with the mentor choosing to work with the mentee, and in a bid to solve the vascular leakage and other toxicity problems associated with DAB-IL-2, they partnered with Drew Pardoll, M.D., Ph.D., director of the Bloomberg~Kimmel Institute for Cancer Immunotherapy.
“The current study demonstrates what we believe is the continuing potential of this agent as a molecule able to re-establish the balance of the immune system in the treatment of solid tumors such as melanoma,” says Murphy. In their paper, Bishai, Murphy, Pardoll and colleagues describe their production of two second-generation forms of the engineered toxins, DAB-IL-2: s-DAB-IL-2 and s-DAB-IL-2(V6A). The V6A form substitutes an amino acid associated with vascular leak syndrome, resulting in a 50-fold reduction of the syndrome in test tube studies.
Treg cells emit powerful immune suppressive signals to the immune system which serve to protect tumor cells. By killing Tregs, s-DAB-IL-2 and s-DAB-IL-2(V6A) remove the suppressive signals and unleash potent immune responses against the tumor (Credit: Johns Hopkins Kimmel Cancer Center)
For the mouse experiments, the team first injected the animals with either regular s-DAB-IL-2 or the V6A form seven and 10 days after being injected with tumor cells.
Both drugs depleted T regulatory cells in the lymph nodes by 50 percent and inhibited tumor growth by 75 percent when evaluated 24 days after the first tumor cell injection. Then, they tried using these proteins followed by an anti-PD-1 checkpoint inhibitor. Mice with melanoma tumors were treated 10 days after tumor initiation with either a control drug, the checkpoint inhibitor, s-DAB-IL-2 or s-DAB-IL-2(V6A) as solo therapies.
Other mice were treated on days 10 and 13 with s-DAB-IL-2 or s-DAB-IL-2(V6A) and then with anti-PD-1 on days 11, 14 and twice a week after that.
When used alone in more advanced tumors, anti-PD-1, s-DAB-IL-2 and s-DAB-IL-2(V6A) had a modest effect on tumors, but when administered as a sequential therapy with anti-PD-1, both s-DAB-IL-2 and s-DAB-IL-2(V6A) had what Bishai calls a “remarkable” inhibition of tumor growth, showing a 10-fold reduction in tumor size.
Examining tumors removed from the mice, the investigators noted a significant increase in interferon gamma-producing CD8 T-cells, important anti-tumor effector cells.
In additional studies, the team has created an alternate form of the protein that removes IL-2 and substitutes other targeting proteins. This compound has shown some promise in laboratory studies of breast cancer in mice, Bishai says.
Coauthors were Laurene Cheung, Juan Fu, Pankaj Kumar, Amit Kumar, Michael Urbanowski, Elizabeth Ihms, Sadiya Parveen, C. Bullen and Garrett Patrick of Johns Hopkins, and Robert Harrison of Northeastern University in Boston.
The work was supported by the National Institutes of Health (grants R21 AI130595, R01 AI36973, R01 HL133190 and P30 CA00693); Maryland TEDCO (Project #0916-006); the Abell Foundation; the Cigarette Restitution Fund; and The Bloomberg~Kimmel Institute for Cancer Immunotherapy.
COI: Murphy, Pardoll and Bishai hold positions in Sonoval LLC, which holds rights to develop s-DAB-IL-2(V6A). These relationships are being managed by The Johns Hopkins University in accordance with its conflict of interest policies.