Worms Wiggle Into Gene Therapy
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Egg secretions from a worm that causes a deadly human disease may prove useful in gene therapy, according to research presented at the British Pharmaceutical Conference (BPC) in Manchester.
Gene therapy is a method of correcting faulty genes responsible for certain diseases, particularly cancers. It involves using a carrier, or 'vector', to insert new genetic material to mend a faulty gene in the affected cells of the person or 'host'. To achieve this, the vector must be able to survive the host's various defence systems and travel through the cell to its nucleus, which holds the host's genes. Gene therapy has great potential, but currently there are no treatments available on the market as the method is complicated and is still being investigated.
The study by pharmacy researchers focuses on Schistosoma mansoni - a worm which is rife in Asia, Africa and South-America - that penetrates human skin to infect the lungs, liver, intestines, bladder, and possibly other organs. The study focused on a protein called IPSE, which is released in large amounts by the worm's eggs into the surrounding tissues, and enters host cells. The study shows that once inside host cells, IPSE rapidly enters the nucleus and can bind to DNA. A very small portion of IPSE can drag much larger proteins through the nuclear pores into the nucleus with it. IPSE therefore has a natural ability to pass right into the cell nucleus and bind with the host genetic material, which makes it a promising option for gene delivery.
University of Nottingham School of Pharmacy PhD student, Ishwinder Kaur, said: "The worm attracted the team's interest because to survive in their hosts, successful parasites have evolved sophisticated ways of evading and/or manipulating their host's immune response. Schistosomes can survive for more than a decade in their host. So, studying how the parasite interacts with its host's immune system can give us valuable clues as to how to exploit strategies honed by millions of years of evolution."
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Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.
Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.
