Vaccine
Abstract
The invention relates to a replication deficient simian adenoviral vector C7 encoding a protein comprising CS protein from P. falciparum or a fragment thereof, for example as shown in Seq ID No: 1 or Seq ID No: 3. The invention also relates to processes of preparing said viral vector and use of the viral vector in the treatment/prevention of malaria infection. Compositions, vaccines and kits comprising said viral vector are also described. In one aspect the invention employs a synthetic C7 viral vector. The C7 viral vector according to the invention may be co-administered or co-formulated with a malaria antigen such as RTS,S optionally in the presence of an adjuvant for example comprising 3D-MPL and/or a saponin such as QS21.
Claims
exact text as granted — not AI-modified1 . A replication deficient simian adenoviral vector C7 encoding a protein comprising CS protein from P. falciparum or an immunogenic fragment thereof.
2 . The adenoviral vector of claim 1 , wherein the protein encoded comprises the sequence of Seq ID No: 7.
3 . The adenoviral vector of claim 1 , where the encoded protein encoded comprises the sequence of Seq ID No: 8.
4 . The adenoviral vector any one of claim 1 , wherein the encoded protein has the sequence of Seq ID No: 1.
5 . The adenoviral vector of claim 1 , wherein the encoded protein has the sequence of Seq ID No: 3.
6 . A pharmaceutical composition comprising the adenoviral vector of claim 1 and an excipient.
7 . An immunogenic composition for the treatment or prophylaxis of malaria comprising the adenoviral vector of claim 1 and an adjuvant.
8 . The immunogenic composition of claim 7 , which further comprises a protein.
9 . The immunogenic composition of claim 8 , wherein the protein is RTS,S.
10 . An immunogenic composition comprising
(1) a replication deficient simian adenoviral vector C7 encoding a protein comprising CS protein from P. falciparum or an immunogenic fragment thereof, (2) a malaria antigen, and (3) an adjuvant.
11 . A kit comprising
(1) a replication deficient simian adenoviral vector C7 encoding a protein comprising CS protein from P. falciparum or an immunogenic fragment thereof, (2) a malaria antigen, and (3) an adjuvant.
12 . The immunogenic composition of claim 10 , wherein the protein encoded by the adenoviral vector C7 has the sequence of Seq ID No: 1.
13 . The immunogenic composition of claim 10 , wherein the malaria antigen is RTS,S.
14 . The immunogenic composition of claim 10 , wherein the adjuvant comprises 3D-MPL.
15 . The immunogenic composition of claim 10 , wherein the adjuvant comprises a saponin.
16 . The immunogenic composition of claim 15 , wherein the saponin is QS21.
17 . The immunogenic composition of claim 10 , wherein the adjuvant comprises 3D-MPL and QS21.
18 . The immunogenic composition of claim 10 , wherein the composition is an oil-in-water emulsion.
19 . The immunogenic composition of claim 10 , wherein the composition is a liposomal formulation.
20 . The immunogenic composition of claim 10 comprising
(1) a replication deficient simian adenoviral vector C7 encoding a protein comprising CS protein from P. falciparum having the sequence of Seq ID No: 1, (2) malaria antigen RTS,S, and (3) an adjuvant comprising 3D-MPL and QS21.
21 . A process for the preparation of a the adenoviral vector of claim 1 comprising the steps of:
a. propagating the adenoviral vector on a suitable cell line, and b. recovering the adenoviral vector.
22 . A process for the preparation of a composition of the immunogenic composition of claim 10 comprising the step of admixing the adenoviral vector of claim 1 with at least one excipient/carrier.
23 . (canceled)
24 . (canceled)
25 . (canceled)
26 . A method of treatment or prophylaxis of malaria in a subject comprising administering to a subject in need thereof a therapeutically effective amount of the immunogenic composition of claim 10 .
27 . A method for the treatment or prophylaxis of malaria in a subject comprising administering to a subject in need thereof a therapeutically effective amount of the adenoviral vector of claim 1 .
28 . The method of claim 27 , wherein the adenoviral vector is administered to the subject in a prime-boost regime.Cited by (0)
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