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Many targeted cancer therapies suppress T cell immune responses

A new 'superagonist' can help overcome these immunosuppressive effects while preserving the powerful anti-cancer benefits of these drugs

In many cases, targeted therapies for cancer are preferred as treatments over chemotherapy and surgery because they attack and kill cancer cells with specific tumour-promoting mutations while sparing healthy, normal cells that do not express these mutations.

In clinical trials, a heavy emphasis on the effects of targeted therapies on tumour cells has been explored, but the effects they have on the immune system have not been thoroughly investigated.

However, new research from The Wistar Institute demonstrated that dozens of these targeted therapies suppressed the activity of T cells that could actually help fight tumours.

While studying the FDA-approved targeted therapy trametinib, the researchers also found that pairing it with a signalling protein "superagonist" stimulated T cell activity while preserving the cancer-blocking effects of the cancer treatment. Study results are published in the journal Cancer Research.

"We wanted to know what the consequences to the immune system were when tumour cells were exposed to targeted therapies," said José R. Conejo-Garcia, M.D., Ph.D., professor and program leader in the tumour Microenvironment and Metastasis program at The Wistar Institute and senior author of the study.

"The effect that these drugs have on the interplay between tumour cells and leukocytes, which are essential for controlling the growth of immunogenic tumours, must be understood if we are to maximize the benefits of combination or sequential administration of targeted therapies and immunotherapies."

Conejo-Garcia and colleagues studied 41 different small molecule inhibitors and their effects on healthy human T cells, which defend the body from pathogens and cancer cells. Every targeted therapy tested in this study inhibited T cells more potently than cancer cells.

In particular, they noticed that the FDA-approved drug trametinib (Mekinist) - a MEK1/2 inhibitor approved to treat metastatic melanoma with a BRAFV600E/K mutation, which affects almost half of all patients with melanoma, was a particularly powerful inhibitor of T cell activity.

The researchers speculated that if cell signaling proteins called cytokines could promote signaling on immune cells but not tumour cells, they could then rescue the T cells from the negative effects of treatment with trametinib.

Cytokines that are commonly administered to patients showed protective activity.

They identified interleukin-15 (IL-15) as an appropriate cytokine to study with trametinib because it promotes stronger signaling activity for effector T cells while not expanding the population regulatory T cells that could suppress the activity of effector T cells.

Conejo-Garcia and colleagues tested an IL-15 "superagonist" currently in phase I and II clinical trials called ALT-803 to determine if this drug could rescue T cells suppressed by trametinib.

When they tested the effects in vivo, they found that T cell proliferation was no longer affected by trametinib. The results confirmed both the inhibitory effect of trametinib on T cells and the ability of IL-15 to overcome this suppression.

"MEK inhibitors like trametinib are being tested in a variety of tumours, and we've demonstrated an effective means of controlling the effect that these drugs have on T cells that could further help in the fight against cancer," said Michael Allegrezza, a predoctoral trainee in the Conejo-Garcia lab and first author of the study. "We plan to continue to study the effects of targeted therapies on the tumour microenvironment and see if other immune cells are impacted in the manner we observed in effector T cells."

The Wistar Institute's business development team is actively seeking a co-development partner to assist in realizing the clinical benefit of the combination of MEK inhibitors and IL-15 superagonists.

Article: IL-15 AGONISTS OVERCOME THE IMMUNOSUPPRESSIVE EFFECTS OF MEK INHIBITORS 

Source: The Wistar Institute

 

 

 

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