(A) Neutropenic animals were co-administered VSX-1 and bacteria (ATCC 27853). The CFU burden in the lung was measured at eight hours. Co-administration of 10 μg of VSX-1 resulted in a multi-log reduction in bacterial burden, with reduction to the limit of detection upon administering 200 μg of ADC. (B) Neutropenic animals were infected with P. aeruginosa (ATCC 27853) and were treated 1 hour post-infection with either vehicle or VSX-1 (200 μg). The CFU burden in the lungs was measured just before treatment (pre-treatment) and eight hours post-injection. (C) The acute lung infection model with P. aeruginosa PA14 (2x106 CFU/animal, 1x106 in each nostril), C57/Bl6, 10 animals per group (two experiments with 5 animal per group each time), intran...
AbstractBackgroundWe sought to characterise a refined rat model of respiratory infection with P. aer...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...
(A)In vitro killing of P. aeruginosa PAO1 in the presence of PMN and complement (OPKA) by VSX. The l...
<p>B6 mice received intra-nasal instillation of 40 µL of <i>P. aeruginosa</i> strain 2310.55 (10<sup...
(A) Activity of VSX-2 compared with VSX-1 with regard to bacterial killing, red blood cell hemolysis...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
Background P. aeruginosa possesses antibiotic resistance, making treatment difficult. Polyclonal ant...
<p>Wild type C57Bl/6 mice were weighed, then inoculated with 3×10<sup>7</sup> cfu of <i>P. aeruginos...
<p>B6 mice were immunosuppressed with cyclophosphamide (100 mg/kg) and 3 days later infected by intr...
<p>(<b>A</b>) C57BL/6 mice were injected (i. p.) with <i>P. aeruginosa</i> PAO1 or 15159 followed by...
AbstractBackgroundWe sought to characterise a refined rat model of respiratory infection with P. aer...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...
(A)In vitro killing of P. aeruginosa PAO1 in the presence of PMN and complement (OPKA) by VSX. The l...
<p>B6 mice received intra-nasal instillation of 40 µL of <i>P. aeruginosa</i> strain 2310.55 (10<sup...
(A) Activity of VSX-2 compared with VSX-1 with regard to bacterial killing, red blood cell hemolysis...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
International audienceDue to growing antibiotic resistance, pneumonia caused by Pseudomonas aerugino...
Background P. aeruginosa possesses antibiotic resistance, making treatment difficult. Polyclonal ant...
<p>Wild type C57Bl/6 mice were weighed, then inoculated with 3×10<sup>7</sup> cfu of <i>P. aeruginos...
<p>B6 mice were immunosuppressed with cyclophosphamide (100 mg/kg) and 3 days later infected by intr...
<p>(<b>A</b>) C57BL/6 mice were injected (i. p.) with <i>P. aeruginosa</i> PAO1 or 15159 followed by...
AbstractBackgroundWe sought to characterise a refined rat model of respiratory infection with P. aer...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...
International audienceThe potential gain in efficacy of pulmonary administration over IV administrat...