The CRISPR Cas system delivered by adeno-associated virus 9 gene therapy to treat HIV was able to target only the intended DNA and cleared the blood in 6 months.
The first in-human trial of a CRISPR Cas system delivered by adeno-associated virus 9 gene therapy to treat HIV was able to target only the intended DNA and cleared the blood within 6 months.
The therapy has its target, Presti explained,"but obviously we're continuing to follow these patients." "I think with the next-generation products, we could get more efficient targeting of the vector; we could improve the specificity of the therapy as well."
HIV Disease HIV Genomics Genomic Medicine CRISPR Clustered Regularly Interspaced Short Palindromic CRISPR-Cas9 Gene Therapy Biologic Therapy Biologics Blood Cd4 Cluster Of Differentiation 4 Cluster Of Differentiation 4 - Cd4 AIDS Acquired Immune Deficiency Syndrome AIDS - Acquired Immune Deficiency Syndrome Clinical Research Clinical Trials Clinical Studies
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