Immunized intranasally
Witryna1 maj 1996 · The protective roles of influenza viral nucleoprotein (NP), together with the cellular mechanism of the protection in the nasal site, were examined in BALB/c mice immunized intranasally with an adjuvant (cholera toxin B subunit containing 0.2% of the whole toxin)-combined A or B virus recombinant NP. Witryna18 lis 2024 · Figure 2. preF-specific serum and mucosal antibody responses in BALB/c mice following immunizations.BALB/c mice (n = 5) were immunized intranasally with recombinant adenovirus (1 × 10 10 VP/mouse).On the 21 st day after immunization, the preF-specific IgG and IgA were detected by ELISA. Serum anti-preF IgG and anti …
Immunized intranasally
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Witryna19 godz. temu · This lack of an apparent booster effect by a second intranasal dose, was not due to an anti-Ad5 vector response caused by the first dose, because mice that received the same i.n. dose of a mock Ad5-vaccine (encoding β-galactosidase) could be efficiently immunized by Ad5-RBD administered intranasally 3 weeks later. WitrynaThe addition of zymosan (10 microg) as an adjuvant in mice which were immunized intranasally with a poly (I:C) (1-5 microg)-combined vaccine (1 microg) enhanced the …
WitrynaMice intranasally immunized with a recombinant 16-kilodalton antigen from roundworm Ascaris parasites are protected against larval migration of Ascaris suum ... As16 was … Witryna6 paź 2015 · Mice were divided into four treatment groups and immunized intranasally as follows: 1) PBS, 2) liposomes alone, 3) OVA alone, or 4) OVA in combination with liposomes (unless otherwise indicated, we used liposomes with 100 μm diameter). Each group of mice was immunized once weekly. To monitor the induction of serum …
Witryna5 mar 2024 · After intranasally challenged with 5 × 105 CFU of Brucella melitensis (strain 16 M), the bacterial loads in lung of the immunized mice were significantly lower than control group. Witryna22 sie 2013 · Mice were immunized with either species D Ad26 (A), Ad28 (B) or Ad48 (C). Three weeks after immunization the mice were anesthetized i.p. with ketamine (140 mg/kg)/xylazine (5.55 mg/kg). The mice were challenged intranasally with 100MLD 50 of influenza A/PR/8/34. The mice were weighed for baseline measurements.
Witryna12 gru 2024 · Mice immunized intramuscularly or intraperitoneally lost weight to a similar extent as naïve mice and succumbed to infection, whereas intranasally immunized mice were protected from substantial weight loss and more than 80% of the mice survived (Fig. 7F). Taken together, intranasal, but not systemic, immunization …
tshock armWitrynaThe protection was detected as early as day 3 following the genital challenge infection and the orally immunized mice were protected from any significant pathology in the upper genital tract. ... The orally vaccinated mice were protected from both lung infection and systemic toxicity caused by intranasally inoculated wild-type C. muridarum ... philtiteWitrynaAntibody-independent, interleukin-17A-mediated, cross-serotype immunity to pneumococci in mice immunized intranasally with the cell wall polysaccharide Infect … tshockbossWitryna28 paź 2024 · Figure 2 Intranasal immunization with heat inactivated virus protects infant mice against lethal challenge. Mice aged 14–17 days of life were immunized intranasally (Bold Dk blue, n=16) or intramuscularly (Lt blue, n=28) with 5 × 10 5 EIU heat inactivated PR8 virus, or left unimmunized (dotted lines, n=13). Three weeks … phil-tite spill bucketWitryna8 gru 2024 · Mice were intranasally or subcutaneously immunized 24 hours later with 10 μg of OVA (Sigma-Aldrich) and 1 μg of LPS (Invivogen), as indicated. MedLN or IngLN was harvested 3 days (T cell proliferation) or 6 days after immunization (Tfh and T H 1 cell analysis), and single-cell suspensions were prepared, stained, and then … tshock disable spawn protectionWitrynaAdministration of the vaccine through an intranasal route failed to overcome prior ADV immunity. Animals exposed to ADV prior to vaccination displayed substantially … t shock euWitrynaImportantly, intranasally immunized mice showed higher neutralizing antibodies and displayed no proinflammatory cytokine IFN-γ in the spleen. Mice were completely protected from a lethal challenge infection with the highly virulent T. gondii (RH) showing no body weight loss (100% survival). Our study shows the effective protection against … phil. titel