Norway


Viruses are quick replicators and that makes them suitable candidates for gene therapy. Typically, modify viral DNA so it17;s no longer pathogenic, and use the virus as a carrier to deliver the 16;correct17; DNA into damaged . It’s a highly meticulous and costly process, and there’s a risk viruses will insert new genes erratically or even disrupt existing, healthy genes. The UCSF approach, however, means a virus may no longer be required.

Instead, an electrical field makes T cell membranes more permeable (temporarily), and to accept CRISPR-edited DNA. Previous research attempts usually meant inserting long strands of DNA into T cells — which are for the body’s immune response — however, this technique caused the cells to perish. On the other hand, CRISPR acts like a molecular snipping tool that selectively identifies and removes erroneous DNA sequences before the repaired sequences can be integrated, making it a much more specific form of gene therapy.

The researchers have already found success in using the modified T cells to a tackle rare disease, that until now, has been resistant to any kind of therapies. Medical student Theo Roth said the new CRIPSR method would R;significantly speed up the of future generations of cell therapy.”

CRISPR’s potential applications are multifold — scientists have used it to increase natural crop yield in rice, develop treatments for sickle cell anemia, and detect HPV and Zika Virus, but it seems there’s work to be done before CRISPR approaches become routine treatment in humans.



Source link

LEAVE A REPLY

Please enter your comment!
Please enter your name here