Stealth virus for cancer therapy

Viral Oncology: Stealth virus for cancer therapy

Scientists have redesigned an adenovirus for use in cancer therapy. They have developed a new protein shield that hides the virus and protects it from being eliminated. Adapters on the surface of the virus enable the reconstructed virus to specifically infect tumour cells.
             Viruses have their own genetic material which can infect human cells in a very specific manner. They will then reproduce as directed by their own genes but using the resources of the host cell. These properties proofs that they can fight with hereditary diseases or cancer. There are uncountable different viruses, but the human adenovirus 5, which normally causes the symptoms of a typical cold, has substantial advantages. Without any of the viral genes
left, the virus cannot replicate and trigger diseases. In addition, the genome of the adenovirus is very large and does not assimilate into human chromosomes.
Adapter molecules dock the virus to the tumor
Until now the use of adenoviruses in tumor therapy has not been employed. Because they lack the ability to infect cancer cells and therefore cannot inject the genetic blueprints for the therapeutic molecules to fight the disease. Moreover, adenoviruses are normally neutralized by the immune system and very rapidly eliminated by the liver. Researchers are now rebuilding the viruses so that they effectively recognize and infect tumor cells. For this purpose they are creating molecules which act as an adapter between the virus and the tumor cell.
         The adapters, which cling very tightly to the coat of the virus, can bind to different surface molecules on the tumor cell. The scientists are testing adapters for several receptors such as HER2 and EGFR, which are present on various types of cancer cells.
New protein shield masks and protects against the immune system
Researchers hid the virus under a novel protein coat, which serves as camouflage for the virus and which protects it from the immune system. As a basis for this shield the researchers used an existing antibody that they had already redesigned.
       The protein shield protected the virus from the immune cells & prevented the virus from being eliminated by the liver, which normally quickly removed unmodified adenoviruses from the bloodstream, often making therapeutic applications impossible. The virus redesigned using sophisticated protein engineering techniques, worked & efficiently infected the tumor cells. Using this stealth gene shuttles, the scientists wants to develop novel therapies for different types of cancer. The success of Adenoviruses will help to tackle one of the greatest problems of cancer medicine & therapy.

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