RSV F VLPs AND METHODS OF MANUFACTURE AND USE THEREOF
The present invention relates to the field of isolation of enveloped virus-based virus-like particles (VLPs) free of infectious agents. In preferred examples, the field includes methods of inactivation of infectious agents that do not adversely affect the immunogenicity of the enveloped virus-based VLPs. In certain embodiments, the enveloped virus-based VLPs are produced in insect cell based expression systems.
1 . A preparation of respiratory syncytial virus F polypeptide virus-like particles comprising a respiratory syncytial virus F polypeptide, wherein the virus-like particles do not comprise an enveloped virus core.
2 . A preparation of respiratory syncytial virus F polypeptide virus-like particles comprising a respiratory syncytial virus F polypeptide, wherein the virus-like particles are pleomorphic, of non-uniform size, or of non-uniform shape.
3 . A preparation of respiratory syncytial virus F polypeptide virus-like particles comprising a respiratory syncytial virus F polypeptide, wherein the virus-like particles do not comprise an enveloped virus core forming polypeptide.
4 . The preparation of claim 1 , wherein the virus-like particles comprise mammalian glycosylation.
5 . The preparation of claim 1 , wherein the virus-like particles are substantially non-aggregated with other virus-like particles.
6 . The preparation of claim 1 , wherein the virus-like particles are substantially not associated with viral vector particles.
7 . The preparation of claim 1 , further comprising an adjuvant in admixture with the virus-like particles.
8 . The preparation of claim 7 , wherein the adjuvant is located outside the virus-like particle.
9 . The preparation of claim 7 , wherein the adjuvant is located inside the virus-like particle.
10 . The preparation of claim 7 , wherein the adjuvant is covalently linked to the respiratory syncytial virus F polypeptide to form a covalent linkage.
11 . The preparation of claim 1 , wherein a neutralizing anti-RSV-F antibody binds to the respiratory syncytial virus F polypeptide.
12 . The preparation of claim 11 , wherein the neutralizing anti-RSV-F antibody is 9C5.
13 . A method for producing a population of respiratory syncytial virus F polypeptide virus-like particles, comprising:
(a) providing an expression vector which expresses a respiratory syncytial virus F polypeptide;
(b) introducing the expression vector into a mammalian cell in a media; and
(c) expressing the respiratory syncytial virus F polypeptide to produce the respiratory syncytial virus F polypeptide virus-like particles, wherein the virus-like particles do not comprise an enveloped virus core.
14 . A method for producing a population of respiratory syncytial virus F polypeptide virus-like particles, comprising:
(a) providing an expression vector which expresses a respiratory syncytial virus F polypeptide;
(b) introducing the expression vector into a mammalian cell in a media; and
(c) expressing the respiratory syncytial virus F polypeptide to produce the respiratory syncytial virus F polypeptide virus-like particles, wherein the virus-like particles are pleomorphic, of non-uniform size, or of nonuniform shape.
15 . A method for producing a population of respiratory syncytial virus F polypeptide virus-like particles, comprising:
(a) providing an expression vector which expresses a respiratory syncytial virus F polypeptide;
(b) introducing the expression vector into a mammalian cell in a media; and
(c) expressing the respiratory syncytial virus F polypeptide to produce the respiratory syncytial virus F polypeptide virus-like particles, wherein the virus-like particles do not comprise an enveloped virus core forming polypeptide.
16 . The method of claim 13 , further comprising the step of recovering the respiratory syncytial virus F polypeptide virus-like particles from the media in which the mammalian cell is cultured.
17 . The method of claim 13 , wherein the expression vector is a viral vector.
18 . The method of claim 17 , wherein the viral vector is selected from the group consisting of: an adenovirus, a herpesvirus, a poxvirus and a retrovirus.
19 . The method of claim 13 , wherein the mammalian cell is selected from the group consisting of a BHK cell, a VERO cell, an HT1080 cell, an MRC-5 cell, a WI 38 cell, an MDCK cell, an MDBK cell, a 293 cell, a 293T cell, an RD cell, a COS-7 cell, a CHO cell, a Jurkat cell, a HUT cell, a SUPT cell, a C8166 cell, a MOLT4/clone8 cell, an MT-2 cell, an MT-4 cell, an H9 cell, a PM1 cell, a CEM cell, a myeloma cell, SB20 cell, a LtK cell, a HeLa cell, a WI-38 cell, an L2 cell, a CMT-93, and a CEMX 174 cell.
20 . The method of claim 13 , wherein a neutralizing anti-RSV-F antibody binds to the expressed respiratory syncytial virus F polypeptide.
21 . The method of claim 20 , wherein the neutralizing anti-RSV-F antibody is 9C5.
22 . A method for treating or preventing respiratory syncytial virus infection comprising administering to a subject an immunogenic amount of the preparation of claim 1 .
23 . The method of claim 22 , wherein the administering induces a protective immunization response in the subject.
24 . The method of claim 22 , wherein the administering is selected from the group consisting of subcutaneous delivery, transcutaneous delivery, intradermal delivery, subdermal delivery, intramuscular delivery, peroral delivery, oral delivery, intranasal delivery, buccal delivery, sublingual delivery, intraperitoneal delivery, intravaginal delivery, anal delivery and intracranial delivery.
25 . A pharmaceutical composition comprising an immunogenic amount of the preparation of claim 1 .
26 . The pharmaceutical composition of claim 25 further comprising a pharmaceutically acceptable carrier.
27 . A method for providing protection against respiratory syncytial virus infection comprising administering to a subject an immunogenic amount of the preparation of claim 1 .
28 . The method of claim 27 , wherein the administering is selected from the group consisting of subcutaneous delivery, transcutaneous delivery, intradermal delivery, subdermal delivery, intramuscular delivery, peroral delivery, oral delivery, intranasal delivery, buccal delivery, sublingual delivery, intraperitoneal delivery, intravaginal delivery, anal delivery and intracranial delivery.