Method of producing pharmaceutical compositions comprising immunogenic chikungunya virus CHIKV-Δ5nsP3
The present invention relates to a process for producing an immunogenic live attenuated Chikungunya virus, as well as pharmaceutical compositions comprising the same.
1 . A pharmaceutical composition comprising chikungunya virus (CHIKV)-Δ5nsP3 particles, wherein said pharmaceutical composition comprises:
(i) at least 10 3 CHIKV-Δ5nsP3 particles which express an E2 structural protein as defined by the amino acid sequence of SEQ ID NO: 2; and
(ii) 1-70% CHIKV-Δ5nsP3 particles which express an E2 structural protein having at least one mutation compared with the amino acid sequence of SEQ ID NO: 2,
wherein said at least one mutation is selected from the group consisting of E168K, E247K, H99Y, G55R, H232Y and T230I.
2 . The pharmaceutical composition according to claim 1 , wherein the CHIKV-Δ5nsP3 particles of (ii) express an E2 structural protein having no more than three mutations compared with the amino acid sequence of SEQ ID NO: 2.
3 . The pharmaceutical composition according to claim 1 , wherein the CHIKV-Δ5nsP3 particles of (ii) express an E2 structural protein having no more than two mutations compared with the amino acid sequence of SEQ ID NO: 2.
4 . The pharmaceutical composition according to claim 1 , wherein the CHIKV-Δ5nsP3 particles of (ii) express an E2 structural protein having no more than one mutation compared with the amino acid sequence of SEQ ID NO: 2.
5 . The pharmaceutical composition according to claim 1 , wherein the pharmaceutical composition comprises up to 3×10 4 CHIKV-Δ5nsP3 particles which express the E2 structural protein as defined by the amino acid sequence of SEQ ID NO: 2.
6 . The pharmaceutical composition according to claim 1 , wherein the pharmaceutical composition comprises up to 10 5 CHIKV-Δ5nsP3 particles which express the E2 structural protein as defined by the amino acid sequence of SEQ ID NO: 2.
7 . The pharmaceutical composition according to claim 1 , wherein the pharmaceutical composition comprises 1-50% of CHIKV-Δ5nsP3 particles which express an E2 structural protein having at least one mutation compared with the amino acid sequence of SEQ ID NO: 2.
8 . The pharmaceutical composition according to claim 1 , wherein said CHIKV-Δ5nsP3 particles of (i) comprise an RNA genome corresponding to the DNA sequence of SEQ ID NO: 1.
9 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition induces neutralizing antibodies against CHIKV-Δ5nsP3 in a mouse immunized with said pharmaceutical composition resulting in a mouse serum comprising said neutralizing antibodies, and wherein said mouse serum neutralizes CHIKV infection of Vero cells by at least 80% in an in vitro plaque reduction neutralization assay at a 1:80 serum dilution.
10 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition induces neutralizing antibodies against CHIKV-Δ5nsP3 in a mouse immunized with said pharmaceutical composition resulting in a mouse serum comprising said neutralizing antibodies, and wherein said mouse serum neutralizes CHIKV infection of Vero cells by at least 90% in an in vitro plaque reduction neutralization assay at a 1:80 serum dilution.
11 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition induces neutralizing antibodies against CHIKV-Δ5nsP3 in a mouse immunized with said pharmaceutical composition, resulting in a mouse serum comprising said neutralizing antibodies, and wherein said mouse serum neutralizes CHIKV infection of Vero cells by at least 95% in an in vitro plaque reduction neutralization assay at a 1:80 serum dilution.
12 . The pharmaceutical composition according to claim 1 , which is obtained by production of CHIKV-Δ5nsP3 particles on Vero cells, wherein said production comprises passaging CHIKV-Δ5nsP3 particles comprising an RNA genome corresponding to the DNA sequence of SEQ ID NO: 1 on Vero cells in culture fewer than five times.
13 . The pharmaceutical composition according to claim 12 , wherein said CHIKV-Δ5nsP3 particles are passaged on Vero cells in culture at most three times.
14 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition is a one-shot pharmaceutical composition.
15 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition is a vaccine.
16 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition is provided in a lyophilized form.
17 . The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition is formulated for subcutaneous administration.
18 . The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition comprises a pharmaceutically acceptable excipient.
19 . A method of protection against disease caused by CHIKV in a subject in need thereof, comprising administering to the subject an effective amount of the pharmaceutical composition according to claim 1 .
20 . The method according to claim 19 , wherein the subject is a human subject.