Category Archives: Immuno-Oncology

UCLA Research Shows Chimeric Antigen Receptors May Boost Immune System Response to Fight Cancer

UCLA Research Shows Chimeric Antigen Receptors May Boost Immune System Response to Fight Cancer
UCLA Research Shows Chimeric Antigen Receptors May Boost Immune System Response to Fight Cancer

Tumors have a number of ways to avoid detection and attack by the body’s immune system, making them difficult to eliminate. In a victory for cancer immunotherapy, scientists have created a synthetic protein with the ability to reverse these defenses.

Overcoming Safeguards of Tumor Cells

Most diseased cells carry proteins called antigens that trigger a response from T cells in the immune system, resulting in neutralization of the threat. In contrast, tumor cells secrete immunosuppressive cytokines, and these soluble proteins disable the immune response from T cells.

Chimeric antigen receptor (CAR) T-cell therapy, which received FDA approval in 2017, has been successfully used to treat blood cancers such as leukemia. Unfortunately, these therapies have not had a similar effect on solid tumors.

Making Cancer Work Against Itself

Building on the principle of CARs and their power to counteract the defenses of cancer cells, a team of scientists at UCLA engineered CARs to respond to soluble proteins along with surface-bound antigens. In effect, cancer’s primary weapon ends up acting as an instrument of its own destruction.

Since these CARs are engineered, it opens up the possibility of using this method to create cancer immunotherapy treatments for other applications. The UCLA team has already engineered CARs that respond to various soluble proteins, including transforming growth factor (TGF) beta.

Cancer Immunotherapy: Boosting the Body’s Own Immune System

Our individually developed immunotherapy programs focus on restoring the body’s immune system and its natural defense mechanisms. These programs are non-toxic, without the adverse side effects that often accompany chemotherapy and other traditional cancer treatments.

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Huntington’s Disease Produced Molecules Are Fatal to Cancer Cells

Huntington's Disease Produced Molecules Are Fatal to Cancer Cells
Huntington’s Disease Produced Molecules Are Fatal to Cancer Cells

Could a clue to more effective cancer treatment be found in the biochemistry of another illness? Scientists are hopeful that the gene behind Huntington’s disease could be fatal to cancer cells without harming healthy ones.

What Is Huntington’s Disease?

Huntington’s disease is a genetically inherited condition that destroys nerve cells in the brain. There is currently treatment but no cure for the disorder, which causes a slowly progressive decline in both cognitive and physical abilities.

The faulty gene that triggers Huntington’s disease contains an excessive number of repeats of a certain sequence of nucleotides, which form the building blocks of DNA and RNA. These sequences create small interfering RNAs, which are molecules that attack specific genes crucial for cell survival.

“Assassin Molecules”

Brain cells in particular are vulnerable to the cell death caused by small interfering RNAs. Cancer cells are also highly susceptible, which is thought to be the reason why Huntington’s disease patients have such a low incidence of cancer.

A research team at Northwestern University tested these so-called “assassin molecules” on human and mouse cancer cells, including brain, breast, colon and ovarian, that were grown in a laboratory. The small interfering RNAs killed all cancer cells from both humans and mice.

Researchers were encouraged that the treatment also showed no toxicity to healthy cells. Further testing is underway to find a more targeted form of delivery.

Targeted Cancer Treatment at Issels®

Our individually developed, non-toxic immunotherapy programs focus on destroying cancer cells and their environment while sparing healthy tissues. Contact us for more information about cancer vaccines and other targeted cancer treatment protocols at Issels®.

Ribosomes May be Hijacked to Protein Fuel for Cancers

It's Time to Stop Cancer
It’s Time to Stop Cancer

Cancer cells often have an uncanny ability to hijack the functions of normal body cells. Scientists have focused on this property in the belief that deciphering the process will lead to more effective cancer treatment.

Thanks to the results of a Yale University study, the scientific community may be a little closer to this goal. Discovery of unknown pathways to fuel sources provides insights into the development and growth of cancer.

How Cell Proteins Drive Cancer Growth

Organelles are specialized structures in cells that carry out certain tasks, much like organs do for the human body. One of these organelles, called the nucleolus, produces ribosomes, which in turn manufacture proteins.

Ribosomes can be hijacked by cancer cells to divert protein production in order to fuel cancer growth. In a study published in Cell Reports, Dr. Susan Baserga of Yale University and two of her graduate students screened 18,000 proteins that are vital to nucleoli formation.

A Target for Immunotherapy Cancer Treatment?

Dr. Baserga and her team found 139 proteins that serve as a type of master switching network. The proteins represent countless cellular pathways that control the production of ribosomes. This discovery clarifies the link between ribosomes and cancer as well as the one between ribosomes and certain birth defects known as ribosomopathies.

Personalized Cancer Treatment at Issels®

Our innovative cancer treatments target both the tumor and its microenvironment. Immunotherapy programs at Issels® are created specifically to address a patient’s individual needs.

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Swiss Group Studies Dendritic Cell Vaccines with Artificial Receptors

New Cancer Research Is Improving Treatment
New Cancer Research Is Improving Treatment

One of the challenges doctors face with cancer treatment is designing a program to meet a patient’s unique needs. Immunotherapy for cancer is helping to provide solutions to this problem, such as recent improvements to dendritic cell vaccines.

Immunotherapy: Priming the Body’s Immune System

While the body’s immune system is extremely capable when it comes to fighting viruses, bacteria and other invaders, cancer cells often demonstrate a remarkable ability to evade detection. Immunotherapy works by enhancing the immune system’s power to target and destroy cancer cells.

Dendritic cells are one of the immune system’s “messengers” that present antigens to killer T-cells for destruction. Researchers in Switzerland began looking for a way to improve the effectiveness of dendritic cell vaccines.

Helping the Immune System Recognize Cancer Cells

Prof. Michele De Palma and his team created artificial receptors known as EVIRs, which are inserted in dendritic cells extracted from a patient. Once reintroduced into the patient’s system, the EVIRs are engineered to recognize exosomes that transport molecules between cells, sometimes assisting in the spread of cancer.

As EVIRs capture exosomes, it allows dendritic cells to present antigens on their outer surface, simplifying recognition and attack by killer T-cells. De Palma and his team have dubbed this phenomenon “cross-dressing,” and they’re hoping that the process will improve the specificity of cancer treatment.

Issels®: A Successful Legacy of Immunotherapy for Cancer

At Issels®, we are exclusively focused on immunotherapy for cancer with patients who have advanced or therapy-resistant cancers. Contact us to learn more about our dendritic cell vaccines and other non-toxic, personally tailored immunotherapy treatment programs.

Protein Blocking May Play a New Role in New Testicular Cancer Treatment

Protein Blocking May Play a New Role in New Testicular Cancer Treatment
Protein Blocking May Play a New Role in New Testicular Cancer Treatment

What options does a patient have when traditional forms of cancer treatment fail? In the case of testicular cancer, scientists found a new combination of treatments that may provide added hope.

Overcoming Resistance to Cancer Treatment

Testicular germ cell tumors are a form of cancer found most commonly in younger men. A research team at the Institute of Cancer Research in London, encouraged by earlier work at the facility, examined the function of a certain type of protein in the development of testicular cancer.

The team focused specifically on insulin growth factor receptor-1. They discovered that IGF1R, as the protein is also called, was more active in some testicular cancer cells as opposed to normal tissue. Using chemical inhibitors, the researchers were able to deplete the supply of IGF1R or curtail its activity, thereby reducing cell growth.

In addition, blocking IGF1R activity in previously drug-resistant cells made them more receptive to platinum-based chemotherapy. The team is hopeful that the two treatments, used in tandem, will be more successful in killing testicular cancer cells.

What Does the Future Hold?

Receptor tyrosine kinases, the class of proteins that includes IGF1R, are linked to cell growth and division in several other types of cancer. Clinical trials have tested the use of IGF1R in hopes that they may have positive results in other applications.

Effective Cancer Treatment for Therapy-Resistant Tumors

For decades, Issels® has been helping patients with advanced and therapy-resistant cancer achieve long-term remission. Contact us to learn how we are continuing the legacy of our founder, Dr. Josef M. Issels, who was a pioneer in the field of immunotherapy for cancer.

Seed Money from Give Hope Will Help to Fund Pancreatic Cancer Research

New Cancer Research Is Improving Treatment
New Cancer Research Is Improving Treatment

Nearly everyone in America has been touched by cancer, whether it’s through personal experience or that of a friend or family member. One woman literally turned her loss into hope for continued research in immunotherapy for cancer and other treatments.

Sorrow Gives Rise to Hope

Susan Hunt’s experience came when her best friend Beth was diagnosed with pancreatic cancer. Hunt mourned the time they lost together, but she challenged her grief into Give Hope, the all-volunteer group she founded to raise seed money for continued research into new treatments and possible cures.

When it comes to cancer research, scientists are faced with a catch-22: they need data to present to the big cancer foundations in order to secure research grants, but they require money to generate the data in the first place. Give Hope has provided major funding for pancreatic cancer studies at the University of Cincinnati.

“Bench to Bedside”

Dr. Syed Ahmad of UC’s Cancer Institute used the term “bench to bedside” to sum up the research process. Every idea begins on a laboratory bench, where it’s nurtured with time and resources until it ends up at a patient’s bedside.

According to Hunt, the seed money raised by Give Hope has generated nearly $2 million in pancreatic cancer research funding for UC. University officials explained that after three years, the Cancer Institute receives $35 for every one dollar in seed money.

Immunotherapy for Cancer: The Issels® Difference

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