Your browser doesn't support javascript.
loading
Chitosan alters inactivated respiratory syncytial virus vaccine elicited immune responses without affecting lung histopathology in mice.
Muralidharan, Abenaya; Russell, Marsha S; Larocque, Louise; Gravel, Caroline; Sauvé, Simon; Chen, Ze; Li, Changgui; Chen, Wangxue; Cyr, Terry; Rosu-Myles, Michael; Wang, Lisheng; Li, Xuguang.
Affiliation
  • Muralidharan A; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, Roger G
  • Russell MS; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
  • Larocque L; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
  • Gravel C; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
  • Sauvé S; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
  • Chen Z; Shanghai Institute of Biological Products, 1262 Yan'an W Rd, Changning Qu, Shanghai Shi 200052, China.
  • Li C; National Institutes for Food and Drug Control and WHO Collaborating Center for Standardization and Evaluation of Biologicals, No. 2; Tiantan Xili, Beijing, China.
  • Chen W; Human Therapeutics Portfolio, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario K1N 5A2, Canada.
  • Cyr T; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
  • Rosu-Myles M; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, Roger G
  • Wang L; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, Roger Guindon Campus, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada.
  • Li X; Centre for Biologics Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Sir Frederick G. Banting Research Centre, AL: 2201E, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, Roger G
Vaccine ; 37(30): 4031-4039, 2019 07 09.
Article in En | MEDLINE | ID: mdl-31186190
ABSTRACT
Chitosan is a polysaccharide capable of augmenting immune responses with a proven safety record in animals and humans. These properties make it a potentially attractive agent for the prevention and treatment of infectious disease. Infection by respiratory syncytial virus (RSV) is the leading cause of serious lower respiratory disease in young children throughout the world. There is no licensed vaccine available against RSV whereas inactivated vaccine is known to cause enhanced respiratory disease instead of protection. Here, we investigated whether chitosan administered one or three days post-infection could protect animals against RSV infection and whether it could alter immune responses or immunopathology induced by inactivated RSV vaccine when administered twice before RSV infection. We found chitosan could modestly protect animals against RSV infection when given post-infection, while, in conjunction with inactivated RSV vaccine when given pre-infection, it could significantly reduce RSV infection in mice. Further mechanistic investigation revealed that chitosan enhanced antigen-specific immune responses through augmenting the induction of regulatory T cells, lung resident T cells and neutralizing antibodies while reversing Th2-skewed immune responses induced by inactivated RSV vaccine but, surprisingly, failing to reverse lung histopathology. Overall, this study sheds more light on the molecular mechanisms underlying inactivated RSV vaccine-induced disease.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Respiratory Syncytial Virus, Human / Respiratory Syncytial Virus Infections / Respiratory Syncytial Virus Vaccines / Chitosan / Lung Limits: Animals Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Respiratory Syncytial Virus, Human / Respiratory Syncytial Virus Infections / Respiratory Syncytial Virus Vaccines / Chitosan / Lung Limits: Animals Language: En Year: 2019 Type: Article