Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters











Database
Language
Publication year range
1.
Vaccine ; 39(3): 487-494, 2021 01 15.
Article in English | MEDLINE | ID: mdl-33357957

ABSTRACT

Colonization factors or Coli surface antigens (CFs or CS) are important virulence factors of Enterotoxigenic E. coli (ETEC) that mediate intestinal colonization and accordingly are targets of vaccine development efforts. CS6 is a highly prevalent CF associated with symptomatic ETEC infection both in endemic populations and amongst travelers. In this study, we used an Aotus nancymaae non-human primate ETEC challenge model with a CS6 + ETEC strain, B7A, to test the immunogenicity and protective efficacy (PE) of a recombinant CS6-based subunit vaccine. Specifically, we determined the ability of dscCssBA, the donor strand complemented recombinant stabilized fusion of the two subunits of the CS6 fimbriae, CssA and CssB, to elicit protection against CS6 + ETEC mediated diarrhea when given intradermally (ID) with the genetically attenuated double mutant heat-labile enterotoxin LT(R192G/L211A) (dmLT). ID vaccination with dscCssBA + dmLT induced strong serum antibody responses against CS6 and LT. Importantly, vaccination with dscCssBA + dmLT resulted in no observed diarrheal disease (PE = 100%, p = 0.03) following B7A challenge as compared to PBS immunized animals, with an attack rate of 62.5%. These data demonstrate the potential role that CS6 may play in ETEC infection and that recombinant dscCssBA antigen can provide protection against challenge with the homologous CS6 + ETEC strain, B7A, in the Aotus nancymaae diarrheal challenge model. Combined, these data indicate that CS6, and more specifically, a recombinant engineered derivative should be considered for further clinical development.


Subject(s)
Enterotoxigenic Escherichia coli , Escherichia coli Infections , Escherichia coli Proteins , Escherichia coli Vaccines , Animals , Antibodies, Bacterial , Antigens, Bacterial/genetics , Aotidae , Enterotoxins/genetics , Escherichia coli Infections/prevention & control , Escherichia coli Infections/veterinary , Escherichia coli Proteins/genetics
2.
Science ; 287(5457): 1506-8, 2000 Feb 25.
Article in English | MEDLINE | ID: mdl-10688803

ABSTRACT

Humans and animals confuse lateral mirror images, such as the letters "b" and "d," more often than vertical mirror images, such as the letters "b" and "p." Experiments were performed to find a neural correlate of this phenomenon. Visually responsive pattern-selective neurons in the inferotemporal cortex of macaque monkeys responded more similarly to members of a lateral mirror-image pair than to members of a vertical mirror-image pair. The phenomenon developed within 20 milliseconds of the onset of the visual response and persisted to its end. It occurred during presentation of stimuli both at the fovea and in the periphery.


Subject(s)
Neurons/physiology , Temporal Lobe/physiology , Visual Cortex/physiology , Visual Perception , Animals , Macaca , Pattern Recognition, Visual , Visual Fields
3.
Am J Physiol ; 272(1 Pt 1): L124-31, 1997 Jan.
Article in English | MEDLINE | ID: mdl-9038911

ABSTRACT

Nitric oxide (NO) is thought to be an important modulator of airway function in normal and inflamed airways. We investigated the acute and chronic effects of induced allergic airway inflammation on NO levels in mixed expired gas and NO synthase (NOS) expression in guinea pigs and the relationship between airway responses and NO production. Airway inflammation was induced by repeated aerosolized antigen exposure, and its presence was confirmed by bronchoalveolar lavage. Acute antigen exposure in sensitized animals produced a fivefold increase in respiratory resistance over baseline that was associated with a cotemporal increase in expired NO (17 +/- 1 to 56 +/- 8 parts per billion, P < 0.01). A continuous subcutaneous infusion of nitro-L-arginine methyl ester (L-NAME), a competitive inhibitor of NOS, markedly decreased expired NO (P < 0.01) and resulted in a significantly greater rise in resistance following antigen challenge (660 +/- 60 vs. 497 +/- 42% of baseline in non-L-NAME-treated animals, P < 0.05). These data support the hypothesis that endogenous pulmonary NO production, as reflected by expired NO, has an important homeostatic role in acute allergic bronchoconstriction.


Subject(s)
Bronchitis/metabolism , Hypersensitivity/metabolism , Nitric Oxide/biosynthesis , Pneumonia/metabolism , Pulmonary Alveoli , Acute Disease , Administration, Inhalation , Animals , Antigens/immunology , Cholinergic Antagonists/pharmacology , Chronic Disease , Enzyme Inhibitors/pharmacology , Guinea Pigs , Hypersensitivity/immunology , Male , NG-Nitroarginine Methyl Ester/pharmacology , Neuropeptides/antagonists & inhibitors , Nitric Oxide Synthase/antagonists & inhibitors , Trachea/immunology , Vagotomy
SELECTION OF CITATIONS
SEARCH DETAIL