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1 fluenced the prevalence of antibodies to the rabies vaccine.
2 99 to receive RTS,S/AS01 and 101 to receive rabies vaccine.
3 ping potential therapeutics and an avirulent rabies vaccine.
4 guide the development of a single-dose human rabies vaccine.
5 s, were randomized to receive RTS,S/AS01E or rabies vaccine.
6 r (GM-CSF) can enhance the immunogenicity of rabies vaccines.
7 hich will help in designing more efficacious rabies vaccines.
8 implications in the development of efficient rabies vaccines.
9 crease our ability to produce more-effective rabies vaccines.
10 need to develop single-dose and long-lasting rabies vaccines.
11 which may help in designing more-efficacious rabies vaccines.
14 ecombinant glycoprotein (rgp) 120 or subunit rabies vaccine administered by the intramuscular route.
15 d in the form of an effective oral wild-life rabies vaccine, although no product for humans has been
16 al immune responses to two priming antigens, rabies vaccine and an adenovirus-based severe acute resp
17 el highlights the safety of third generation rabies vaccines and serves as a platform for standardize
18 omising candidate vector for a transmissible rabies vaccine, and provide a framework to discover and
19 ly a total of 81 (57.0%) tested positive for rabies vaccine antibodies, possibly, due to the delayed
23 ovide a basis from which to develop improved rabies vaccines based on RABV-G stabilized in the prefus
24 receive three doses of either RTS,S/AS01 or rabies vaccine (both 0.5 mL per dose by intramuscular in
25 This is first report of an orally effective rabies vaccine candidate in animals based on PIV5 as a v
26 ChAdOx2 RabG, a simian adenovirus-vectored rabies vaccine candidate, might have potential to provid
27 n naive volunteers during a 3-dose course of rabies vaccine compared with the B-cell response to a bo
28 oculating a single bat with a DrBHV-vectored rabies vaccine could immunize >80% of a bat population,
29 andidate for a new generation of recombinant rabies vaccine for humans and animals and PIV5 is a pote
32 orld Health Organization (WHO) pre-qualified rabies vaccines for humans are inactivated tissue cultur
33 ith the B-cell response to a booster dose of rabies vaccine given to previously immunized volunteers.
35 0.1 mL ID of the human diploid cell culture rabies vaccine [HDCV] at days 0 and 7) vs a standard 3-v
37 who received human rabies immune globulin or rabies vaccine in the ED from January 2015 to June 2018
40 prophylaxis using rabies immune globulin and rabies vaccine is effective in preventing rabies followi
42 ministration of the first dose of a licensed rabies vaccine, nine participants had virus neutralising
44 recipients and 37 (36.6%, 27.3-46.8) of 101 rabies-vaccine recipients (relative risk 1.1, 95% CI 0.8
45 1 recipients and four (4.0%, 1.1-9.8) of 101 rabies-vaccine recipients died, but no deaths were deeme
46 1 recipients and 12 (11.9%, 6.3-19.8) of 101 rabies-vaccine recipients had at least one serious adver
47 case of Haemophilus influenza meningitis (1% rabies-vaccine recipients), and one case of tuberculosis
48 of pneumonia (1% RTS,S/AS01 recipients vs 3% rabies-vaccine recipients), five cases of gastroenteriti
49 troenteritis (3% RTS,S/AS01 recipients vs 2% rabies-vaccine recipients), five cases of malnutrition (
50 -vaccine recipients), one case of sepsis (1% rabies-vaccine recipients), one case of Haemophilus infl
51 malnutrition (2% RTS,S/AS01 recipients vs 3% rabies-vaccine recipients), one case of sepsis (1% rabie
52 he gut microbiome in individuals receiving a rabies vaccine, resulting in systemic inflammatory respo
53 71%]; P = .009), administration distant from rabies vaccine site (180 of 254 [71%] to 58 of 70 [83%];
54 ion into wounds, administration distant from rabies vaccine site, and administration that avoids the
58 (1:1:1:1:1) to one of five groups to receive rabies vaccine (the control group) at months 0, 1, and 2
59 ss efficient and unsafe nerve-tissue-derived rabies vaccines, the burden of this disease could be sub
60 ody maintenance then administered a licensed rabies vaccine (to simulate post-exposure prophylaxis) a
61 (PEP) currently comprises administration of rabies vaccine together with rabies immunoglobulin (RIG)
63 emulsion (GLA-SE; 2.5 or 5 mug), or control rabies vaccine (Verorab) were administered intramuscular
67 ration of sequential doses of an intradermal rabies vaccine was shown to result in reduced vaccine im
73 rategy to develop a single-dose postexposure rabies vaccine where the generation of early protective
74 ld be strongly advised to be vaccinated with rabies vaccines, which are effective against EBLV-1.