Non-integrative and non-replicative lentivirus, preparation and uses thereof
View Patent ↗The invention concerns a non-integrative and non-replicative recombinant lentivirus as well as its uses, in particular for preparing a composition for transferring genes in vitro, ex vivo or in vivo. The invention is useful for transferring genes in any mammal organism, for example in liver, muscle, pancreas or central nervous system (including the ocular sphere) tissues or cells, and in particular for treating disorders or pathologies such as, for example, central nervous system, including the ocular sphere, disorders.
1. A non-replicative and non-integrative recombinant lentivirus comprising (i) a recombinant lentiviral genome which does not encode any lentiviral proteins, comprising a 5′ and a 3′ LTR sequence flanking: a lentiviral encapsidation psi sequence, a RNA nuclear export element, a transgene, as well as (ii) a mutated HIV-1 lentiviral integrase wherein the mutation abolishes integrative function of the integrase thereby preventing the integration of the recombinant genome into the genome of a host cell, the mutation consisting of one or more point mutations in the L, Q and/or N regions of the C-terminal basic region of the HIV-1 integrase.
2. The lentivirus according to claim 1 , wherein the recombinant genome further comprises a sequence enabling effective nuclear import of RNA.
3. The lentivirus according to claim 2 , wherein the sequence enabling effective nuclear import of RNA is cPPT CTS.
4. The lentivirus according to claim 1 , wherein said lentivirus is obtained from HIV-1, HIV-2, SIV, FIV, EIAV, BIV, VISNA and CAEV.
5. The lentivirus according to claim 4 , wherein the lentivirus is obtained from HIV-1 and the one or more point mutations is a substitution of the 262 RRK motif by an AAH motif in the HIV-1 integrase sequence.
6. The lentivirus according to claim 1 , wherein the RNA nuclear export element comprises the REV responsive element (RRE sequence) of HIV-1.
7. The lentivirus according to claim 1 , wherein the transgene is a catalytic nucleic acid (interferent, antisense, ribozyme), a suicide nucleic acid or a nucleic acid encoding a biologically active polypeptide.
8. The lentivirus according to claim 1 , wherein the transgene is a nucleic acid encoding a growth factor, a trophic factor, a hormone, a cytokine, an antibody, a receptor, a differentiation factor, a colony stimulation factor, an anticancerous agent, a toxin, an enzyme, a neurotransmitter or its precursor.
9. The lentivirus according to claim 1 , wherein the lentivirus is obtained from HIV-1 and the one or more point mutations is a substitution of amino acid 186 in the L region of the C-terminal basic region.
10. The lentivirus according to claim 1 , wherein the lentivirus is obtained from HIV-1 and the one or more point mutations are Q214L substitution and/or a Q216L substitution in the Q region of the C-terminal basic region.
11. A pharmaceutical composition comprising (a) a non-replicative and non-integrative recombinant lentivirus comprising (i) a recombinant lentiviral genome which does not encode any lentiviral proteins, comprising a 5′ and a 3′ LTR sequence flanking: a lentiviral encapsidation psi sequence, a RNA nuclear export element, a transgene, as well as (ii) a mutated HIV-1 lentiviral integrase wherein the mutation abolishes integrative function of the integrase thereby preventing the integration of the recombinant genome into the genome of a host cell, the mutation consisting of one or more point mutations in the L, Q and/or N basic regions of the C-terminal basic region of the HIV-1 integrase, and (b) a pharmaceutically acceptable excipient.
12. The pharmaceutical composition according to claim 11 , wherein the recombinant genome of the lentivirus further comprises a sequence enabling effective nuclear import of RNA.