Nature Publishing Group, publisher of Nature, and other science journals and reference works NATURE.COM NATURE NEWS NATUREJOBS NATUREEVENTS ABOUT NPG
Help Nature.com site index  
Gene Therapy
SEARCH     advanced search my account e-alerts subscribe register
Journal home
Advance online publication
Current issue
Archive
Press releases
For authors
For referees
Contact editorial office
About the journal
For librarians
Subscribe
Advertising
naturereprints
Contact NPG
Customer services
Site features
NPG Subject areas
Access material from all our publications in your subject area:
Biotechnology Biotechnology
Cancer Cancer
Chemistry Chemistry
Dentistry Dentistry
Development Development
Drug Discovery Drug Discovery
Earth Sciences Earth Sciences
Evolution & Ecology Evolution & Ecology
Genetics Genetics
Immunology Immunology
Materials Materials Science
Medical Research Medical Research
Microbiology Microbiology
Molecular Cell Biology Molecular Cell Biology
Neuroscience Neuroscience
Pharmacology Pharmacology
Physics Physics
Browse all publications
 
August 1999, Volume 6, Number 8, Pages 1448-1455
Table of contents    Previous  Abstract  Next   Full text  PDF
Paper
The effect of CpG sequences on the B cell response to a viral glycoprotein encoded by a plasmid vector
S Pasquini1,2, H Deng1, S T Reddy1, W Giles-Davis1 and H C J Ertl1

1The Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA

2ICRF Molecular Oncology Unit, Hammersmith Hospital, London, UK

Correspondence to: HCJ Ertl

Abstract

The effect of palindromic CpG sequences on the B cell response to plasmid vectors expressing a highly immunogenic viral glycoprotein was investigated. Methylation of the CpG sequences of bacterial expression vectors abolished their ability to induce an antibody response to the transgene product in mice. The antibody response could be rescued by concomitant injection of oligonucleotides carrying immunostimulatory sequences. The B cell response to two plasmid vectors, both expressing the same viral glycoprotein but containing a different content of the highly stimulatory AACGTT motif, was compared. Comparable B cell responses were induced to the two constructs given at an optimal vaccine dose while the vector containing additional palindromic sequences resulted in higher antibody titers at a suboptimal dose. These data indicate that deletion of CpG motifs or methylation of such sequences in plasmid DNA can abrogate the immune response to the vector encoded antigen and might thus enhance their usefulness as gene therapy vehicles.

Keywords

gene therapy; expression vector; CpG sequences; methylation; immune responses

Received 11 December 1998; accepted 15 April 1999
August 1999, Volume 6, Number 8, Pages 1448-1455
Table of contents    Previous  Abstract  Next   Full text  PDF
Privacy Policy © 1999 Nature Publishing Group