Cationic liposome conjugation to recombinant adenoviral vector reduces viral antigenicity
- PMID: 10804282
- PMCID: PMC5926462
- DOI: 10.1111/j.1349-7006.2000.tb00953.x
Cationic liposome conjugation to recombinant adenoviral vector reduces viral antigenicity
Abstract
Adenoviral (Ad) vectors are commonly used in gene therapy trials because of their efficiency in gene transfer. However, their use is limited by immune responses that reduce transgene expression and decrease the efficacy of repeated vector administration. In this study, we demonstrated that conjugation of Ad vector with our novel cationic liposomes could reduce viral antigenicity in vivo. Mice subcutaneously injected with liposome-conjugated Ad vector showed a 6.5-fold reduction of anti-Ad antibodies with neutralizing activity, compared to those with unconjugated Ad vector. Interestingly, we also found that the conjugated vector is less susceptible to inactivation by neutralizing antibodies in vitro and in vivo. Our results suggest that liposome conjugation reduces viral antigenicity, shields vectors from neutralizing antibody, and may allow repeated Ad vector administration.
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References
-
- ) Ali , M. , Lemoine , N. R. and Ring , C. J. A.The use of DNA viruses as vectors for gene therapy . Gene Ther. , 1 , 367 – 384 ( 1994. ). - PubMed
-
- ) Akli , S. , Caillaid , D. , Vigne , E. , Stradford‐Perricaudet , L. D. , Poenaru , L. , Perricaudet , M. , Kahn , A. and Perschanski , M. R.Transfer of a foreign gene into the brain using adenovirus vectors . Nat. Genet. , 3 , 224 – 228 ( 1993. ). - PubMed
-
- ) Bajocchi , G. , Feldman , S. H. , Crystal , R. G. and Mastrangeli , A.Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors . Nat. Genet. , 3 , 229 – 231 ( 1993. ). - PubMed
-
- ) Davidson , B. L. , Allen , E. D. , Kozarsky , K. F. , Wilson , J. M. and Rosessler , B. J.A model system for in vivo gene transfer into the central nervous system using adenoviral vector . Nat. Genet. , 3 , 219 – 223 ( 1993. ). - PubMed
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