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1 e P1 COBRA VLP and either the X3 or X6 COBRA VLP vaccine.
2 strated the immune potency of the formulated VLP vaccine.
3 to a surge of industry interest in exploring VLP vaccines.
4 have benefits for ZIKV and other flaviviral VLP vaccines.
5 cts as compared to those that received WS/05 VLP vaccines.
6 el that previously validated the efficacy of VLP vaccines.
7 cial requirement for validating manufactured VLP vaccines.
8 mically viable than the virus-like particle (VLP) vaccine.
9 intramuscular norovirus virus-like particle (VLP) vaccine.
10 he immunogenicity of a recombinant HPV-16 L1 VLP vaccine administered intramuscularly, without adjuva
12 udy, we describe the development of a dengue VLP vaccine and demonstrate that it induces a robust imm
13 (PBMCs) from 43 individuals receiving the L1 VLP vaccine and from 10 individuals receiving placebo.
15 Whole-inactivated and virus-like particle (VLP) vaccines are 2 of the current approaches being eval
16 mavirus virion protein) virus-like particle (VLP) vaccines are regarded as safe, effective, and well
17 tential applications in the development of a VLP vaccine as well as small-molecule drugs targeting as
18 in the development of a virus-like particle (VLP) vaccine as well as small-molecule drugs targeting a
19 e, study day 22) with a single dose of CHIKV VLP vaccine, based on a four-fold increase of CHIKV neut
21 Interestingly, the potential tetravalent VLP vaccine candidate provided strong neutralizing antib
22 .1 and GII.4c norovirus virus-like particle (VLP) vaccine candidate adjuvanted with alum and monophos
24 ed 2 bivalent norovirus virus-like particle (VLP) vaccine candidate formulations in healthy adults ag
25 da's bivalent norovirus virus-like particle (VLP) vaccine candidate in 50 healthy 18- to 49-year-olds
26 ization, with novel RSV virus-like particle (VLP) vaccine candidates containing stabilized prefusion
29 es are needed to evaluate whether and/or how VLP vaccines confer protection against genital HPV infec
30 recent studies have shown the ability of the VLP vaccines containing GP, NP, and VP40 to confer compl
31 replication and immunity, and shows that NV VLP vaccines could induce protective homologous immunity
33 controlled studies of a virus-like particle (VLP) vaccine derived from norovirus GI.1 genotype adjuva
34 .n.) doses of a rotavirus-like particle (2/6-VLPs) vaccine derived from Wa (VP6) and bovine RF (VP2)
35 double-layered rotavirus-like particle (2/6-VLPs) vaccines derived from simian SA11 or human (VP6) W
36 production is applicable to other flavivirus VLP vaccine development, due to the similarity in viral
37 the research and development that led to the VLP vaccines; discusses their safety, efficacy, and shor
38 re, we demonstrate that virus-like particle (VLP) vaccines elicit a protective neutralizing antibody
40 accinated with a single dose of the COBRA HA VLP vaccines elicited antibodies with HAI activity again
41 ults demonstrate that a novel bivalent Ebola VLP vaccine elicits strong humoral and cellular immune r
44 accinating ferrets with virus-like particle (VLP) vaccines expressing COBRA HA proteins elicited anti
45 s, were vaccinated with virus-like particle (VLP) vaccines expressing either an HA from a wild-type H
47 ed work to date regarding development of the VLP vaccines for prevention of lethal filovirus hemorrha
50 uation of a Pfs47-based virus-like particle (VLP) vaccine generated by conjugating our 58 amino acid
51 volunteers immunized with a multivalent NoV VLP vaccine (genotypes GI.1/GII.4) were analyzed for IgG
53 cacy of the licensed L1 virus-like particle (VLP) vaccines has encouraged development of several seco
58 sults of this study support the use of CHIKV VLP vaccine in individuals with previous alphavirus vacc
59 rticle vaccine was comparable to that of the VLP vaccine in pigs (60%) and to the homologous protecti
61 ccessfully demonstrated efficacy of bivalent VLP vaccines in rodents; more recent studies have shown
62 s in the development of second-generation L1 VLP vaccines in terms of cost reduction-eg, by productio
63 chikungunya virus virus-like particle (CHIKV VLP) vaccine in previous recipients of heterologous alph
64 ibe the construction of virus-like particle (VLP) vaccines in which modified M1, A35 and B6 proteins
65 on with influenza A/PR8 virus-like particle (VLP) vaccine, in vivo and in vitro vaccine antigen-speci
76 ade-specific responses and suggests an HPV16 VLP vaccine may have broader protection that initially a
77 transplant recipients with a multivalent BKV VLP vaccine might reduce the risk of developing posttran
78 te the nanoparticle and virus-like particle (VLP) vaccine molecules from host cell proteins and other
79 ed vaccines or help to re-formulate existing VLP vaccines not naturally carrying immunostimulatory se
83 vercome this, we used a virus-like particle (VLP) vaccine platform (PP7) for conformationally-restric
87 nst virus shedding, while the P particle and VLP vaccines provided cross-variant protection (47% and
92 - and betaHPVs, we developed a two-component VLP vaccine, RG2-VLP, in which L2 protective epitopes de
97 rces for screening or highly multivalent HPV VLP vaccines, suggesting the need for a low-cost, broadl
98 HAI activity after vaccination with COBRA HA VLP vaccines than COBRA preimmune ferrets vaccinated wit
99 development and immunogenicity of SARS-CoV-2 VLP vaccine that incorporates the four structural protei
100 valent, spherical Ebola virus-like particle (VLP) vaccine that incorporates glycoproteins (GPs) from
101 n and use of virus-free virus-like particle (VLP) vaccines that mimic the "empty" capsids (ECs) norma
104 Vaccination with a monovalent HPV-16 L1 VLP vaccine was associated with modulation of genes invo
107 The intranasal monovalent adjuvanted Norwalk VLP vaccine was well tolerated and highly immunogenic an
111 nti-hRSV approaches are virus-like particle (VLP) vaccines, which, based on resemblance to virus or v
112 I) antibody titers than antisera elicited by VLP vaccines with wild-type HA VLPs in preimmune ferrets
113 s GI.1/GII.4 bivalent vaccine-like particle (VLP) vaccine with 3-O-desacyl-4'-monophosphoryl lipid A
115 istered multivalent norovirus-like particle (VLP) vaccines with alphavirus adjuvant particles to mice
116 ally delivered norovirus viruslike particle (VLP) vaccine (with chitosan and monophosphoryl lipid A a