Improving the safety of a conditional-live human immunodeficiency virus type 1 vaccine by controlling both gene expression and cell entry.

Abstract:

:Live attenuated human immunodeficiency virus type 1 (HIV-1) vaccines are considered unsafe because faster-replicating pathogenic virus variants may evolve after vaccination. We previously presented a conditional-live HIV-1 variant of which replication can be switched off as an alternative vaccination strategy. To improve the safety of such a vaccine, we constructed a new HIV-1 variant that depends not only on doxycycline for gene expression but also on the T20 peptide for cell entry. Replication of this virus can be limited to the level required to induce the immune system by transient administration of doxycycline and T20. Subsequent withdrawal of these inducers efficiently blocks viral replication and evolution.

journal_name

J Virol

journal_title

Journal of virology

authors

Das AT,Baldwin CE,Vink M,Berkhout B

doi

10.1128/JVI.79.6.3855-3858.2005

subject

Has Abstract

pub_date

2005-03-01 00:00:00

pages

3855-8

issue

6

eissn

0022-538X

issn

1098-5514

pii

79/6/3855

journal_volume

79

pub_type

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