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Efficacy comparison of adjuvants in PcrV vaccine against Pseudomonas aeruginosa pneumonia
Authors:Saeko Hamaoka  Yoshifumi Naito  Hideya Katoh  Masaru Shimizu  Mao Kinoshita  Koichi Akiyama  Atsushi Kainuma  Kiyoshi Moriyama  Ken J. Ishii  Teiji Sawa
Affiliation:1. Department of Anesthesiology, Kyoto Prefectural University of Medicine, Kyoto 602‐8566, Japan;2. Department of Anesthesiology, School of Medicine, Kyorin University, Mitaka 181‐8611, Japan;3. Laboratory of Adjuvant Innovation, National Institutes of Biomedical Innovation, Health and Nutrition, Ibaraki, Osaka 567‐0085, Japan;4. Laboratory of Vaccine Science, Immunology Frontier Research Center, World Premier International Research Center, Osaka University, Suita, Osaka 565‐0871, Japan
Abstract:Vaccination against the type III secretion system of P. aeruginosa is a potential prophylactic strategy for reducing the incidence and improving the poor prognosis of P. aeruginosa pneumonia. In this study, the efficacies of three different adjuvants, Freund's adjuvant (FA), aluminum hydroxide (alum) and CpG oligodeoxynucleotide (ODN), were examined from the viewpoint of inducing PcrV‐specific immunity against virulent P. aeruginosa. Mice that had been immunized intraperitoneally with recombinant PcrV formulated with one of the above adjuvants were challenged intratracheally with a lethal dose of P. aeruginosa. The PcrV–FA immunized group attained a survival rate of 91%, whereas the survival rates of the PcrV–alum and PcrV–CpG groups were 73% and 64%, respectively. In terms of hypothermia recovery after bacterial instillation, PcrV–alum was the most protective, followed by PcrV–FA and PcrV–CpG. The lung edema index was lower in the PcrV–CpG vaccination group than in the other groups. PcrV–alum immunization was associated with the greatest decrease in myeloperoxidase in infected lungs, and also decreased the number of lung bacteria to a similar number as in the PcrV–FA group. There was less neutrophil recruitment in the lungs of mice vaccinated with PcrV–alum or PcrV–CpG than in those of mice vaccinated with PcrV–FA or PcrV alone. Overall, in terms of mouse survival the PcrV–CpG vaccine, which could be a relatively safe next‐generation vaccine, showed a comparable effect to the PcrV–alum vaccine.
Keywords:bacterial components  infection immunity  toxin  vaccines
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