Recent progress of genetic engineering allows us to create animal mode
ls expressing the new genetic phenotype and also indicates a sure futu
re for clinical use of gene therapy. We applied HVJ-liposome method fo
r manipulation of transforming growth factor (TGF)-beta gene expressio
n in anti-Thy-1 experimental glomerulonephritis. Either the glomerular
introduction of TGF-beta antisense oligodeoxynucleotides or transfect
ion of gene for decorin, a natural inhibitor of TGF-beta, into the ske
letal muscle could suppress the extracellular matrix (ECM) expansion i
n glomerulonephritis. Thus, these results may suggest the potential of
gene therapy as a novel treatment for fibrotic diseases caused by TGF
-beta.