Published in Gene Therapy Weekly, November 20th, 1995
As HIV predominantly infects cells of the hematopoietic system, stem cells are good potential targets for the introduction of foreign anti-HIV genes. Ex vivo transduction, and then reimplantation of the genetically modified stem cells into HIV infected patients could allow the repopulation of the host with mature CD4+ cell populations expressing novel molecules that interfere with viral replication and slow progression into AIDS.
V. Calenda et al., of Transgene and INSERM in France, have developed new gene therapy protocols for the...
Want to see the full article?
Welcome to NewsRx!
Learn more about a six-week, no-risk free trial of Gene Therapy Weekly
Source: Gene Therapy Weekly (1995-11-20)
NewsRx also is available at LexisNexis, Gale, ProQuest, Factiva, Dialog, Thomson Reuters, NewsEdge, and Dow Jones.