Population
Human and rat synoviocytes and chondrocytes and immunocompetent and immunocompromised rats
Design
Preclinical
Follow-up
up to 6 weeks
Authors
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Supports lentiviral gene delivery in arthritis models; leaves open clinical translation from this animal study.
Lentiviral vectors are capable of efficient in vivo gene transfer to the synovium, suggesting potential utility for long-term gene-based treatments of arthritis.
Gouze et al. (2002) studied this question.
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