Cancer Vaccine Strategy Utilizes Interleukin 2 (IL2)

Persistence of IL2 Signaling Enhances the Antitumor Effect of Peptide Vaccines through T-cell Expansion and Preventing PD-1 Inhibition
(Precision Vaccinations News)

New cancer research could be a guideline for constructing vaccines with a greater likelihood of finding and attacking tumors in the human body.

Published in Cancer Immunology Research by Drs. Esteban Celis and Hussein Sultan of the Georgia Cancer Center, the key in this vaccine strategy is increasing the amount of time a cytokine called interleukin 2 (IL2) stays in the body.

IL2 is a molecule in the immune system responsible for regulating the activity of some white blood cells known as ‘killer T cells’.

"After administering peptide-based vaccines in mouse models of cancer, we saw that sustained IL2 signaling dramatically increased the number of tumor-specific cancer-killing T cells (CD8+)," said Dr. Hussein Sultan.

During their experiments, these researchers noticed there was also an increase in the T cells' ability to resist cancer immune evasion caused by a protein called programmed death-ligand 1 (PD-L1)

It is well known that the PD-L1 protein can be produced by tumor cells, allowing them to evade destruction by the killer T cells.

"Together, these results substantially improved the antitumor efficacy of peptide-based vaccines in tumor-bearing mice," Dr. Sultan said.

Dr. Celis added, "In order to be effective, IL2 needed to be administered either as a complex of IL2 and anti-IL2 antibody or in the form of polyethylene glycol-modified IL2 (PEG-IL-2).”

“These formulations prolonged the half-life of IL2, allowing sustained activation of the IL2 receptor on vaccine-generated T cells, allowing them to survive longer in the body and attack the tumor."

According to Dr. Celis, it is difficult for vaccines to induce antibodies against tumors because most of the tumor antigens are not foreign proteins, as is the case with viruses.”

“On the other hand, T cells have the capacity to recognize other types of antigens.”

"As we know, cancer cells are created when normal cells undergo certain mutations," Celis said. "So, they don't always look foreign to our immune system."

Dr. Sultan said, "I want to help the scientific community discover insights on how to use the body's immune system to fight this devastating disease."

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