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1 e response to that elicited by the IpaB/IpaD combination vaccine.
2 o be the highest dose level of 3.0 mg of the combination vaccine.
3 ween monovalent RSV cpts-248/404 vaccine and combination vaccine.
4 sponsiveness of the env DNA component in the combination vaccine.
5 strains in humans could be rectified by this combination vaccine.
6 rs [-13.7 to -11.0]) compared with the other combination vaccines.
7 on vaccine constructs were used to develop a combination vaccine against EBOV, SUDV, and BDBV.
8 d with a TLR3 agonist is feasible, also as a combination vaccine against influenza.
9                         Vaccination with the combination vaccine also led to enhanced E6-specific CD8
10                                              Combination vaccines and simultaneous administration of
11 s received a separate consistency lot of the combination vaccine, and 1 group received separate but c
12 ate for the development of new multipathogen combination vaccines, and suggest ways to accelerate the
13     Despite reduced immunogenicity, DTaP-Hib combination vaccines appear to prime for immunologic mem
14  should stimulate interest in assessing this combination vaccine approach in humans.
15 ine manufacturing infrastructure to generate combination vaccines capable of protecting from both inf
16                          Immunization with a combination vaccine composed of highly purified native F
17                             Furthermore, the combination vaccine conferred significant protection aga
18 ating the potential for the development of a combination vaccine consisting of Invaplex and other imm
19                                            A combination vaccine consisting of TT adsorbed to alum an
20             Here we report the efficacy of a combination vaccine containing gC2/gD2 and UL19/UL47 for
21              In guinea pigs immunized with a combination vaccine containing HIV env and HIV gag DNA p
22 e used for the assessment of new IPVs and of combination vaccines containing an IPV component.
23 ages 2, 3, and 4 months until 2004, when new combination vaccines containing inactivated poliovirus w
24  component of acellular pertussis-containing combination vaccines (DTaP-Hib) is unclear.
25 ) to either a first dose of a pentavalent wP combination vaccine (DTwP-Hib-HepB, Pentabio PT Bio Farm
26 of guinea pigs or ferrets with the trivalent combination vaccine elicited humoral responses to each o
27       Similarly, the EEEV replicon and V/W/E combination vaccine elicited neutralizing antibodies aga
28                        Vaccination with this combination vaccine elicited neutralizing antibodies and
29                                          The combination vaccine elicited protection that was compara
30 -RBD vaccine has the potential to serve as a combination vaccine for inducing sterilizing immunity ag
31 acterization of a recombinant hypoallergenic combination vaccine for specific immunotherapy of HDM al
32 and Dec 31, 2012, either as individual or as combination vaccines, for all age and sex groups.
33 ce to suggest that physicians should not use combination vaccines in ELBW infants.
34                  We previously showed that a combination vaccine incorporating J8-DT (conserved pepti
35 ved as the number of doses of the DTaP/PRP-T combination vaccine increased (P<.02 and P=.01, respecti
36 ears of life has increased, and although new combination vaccines may eventually simplify the schedul
37 a collected from rabbits vaccinated with the combination vaccine neutralized all four targets.
38                  The protection induced by a combination vaccine of AMA1 and MSP1 was not superior to
39 gella is endemic, protection studies using a combination vaccine of Shigella sonnei vaccine strain WR
40 ios (including six single vaccines and three combination vaccines) on antibiotic- treated diarrhoea,
41               The hepatitis A portion of the combination vaccine produced clinically acceptable high
42        Rhesus macaques were immunized with a combination vaccine regimen consisting of adenovirus typ
43  PIV3 vaccine; 16 (76%) of 21 children given combination vaccine shed PIV3-cp45 versus 11 (92%) of 12
44 se results demonstrate the potential of this combination vaccine strategy and suggest that vaccine pr
45  using the chimpanzee model to investigate a combination vaccine strategy involving sequential primin
46                            The DTaP-PRP-T-HB combination vaccine studied elicits high avidity antibod
47                                Incorporating combination vaccines, such as the measles-mumps-rubella-
48                         To create a seasonal combination vaccine targeting both influenza viruses and
49 nes cell envelope proteinase, we developed a combination vaccine that is highly effective in blocking
50 he UK has coincided with the distribution of combination vaccines that contain acellular pertussis (D
51 ty of developing new generations of RV-based combination vaccines that provide protection against a s
52 B vaccine (Engerix-B), and hepatitis A and B combination vaccine (Twinrix) were studied using the VAE
53                           Treatment with the combination vaccine was also shown to enhance the antitu
54                                          The combination vaccine was generally well tolerated.
55 e level of protection afforded by WRSd1 in a combination vaccine was lower than the protection elicit
56 tis-Haemophilus influenza type b-hepatitis B combination vaccine were given at 2, 3, and 4 months aft
57                           Mice receiving the combination vaccine were strongly protected against pyod
58                               CONCLUSION The combination vaccines were safe and effective in elicitin
59 similar across immunization types, including combination vaccines when compared with single-dose vacc
60 d protection with the LION-SUDV and the LION-Combination vaccines, while the LION-EBOV vaccine achiev
61                                              Combination vaccines will probably be necessary to achie
62 or receptor (HER2) extracellular domain in a combination vaccine with a promiscuous T-cell epitope (i
63                                            A combination vaccine with M-cell targeted recombinant HA1