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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2007-2-16
pubmed:abstractText
While evaluating vaccine efficacy against clinical Bordetella pertussis isolates in mice, after challenge vaccinated mice showed increased lung pathology with eosinophilia, compared to challenged, non-vaccinated animals. This led us to study bacterial clearance, lung pathology, lung TNF-alpha expression, and parameters of immediate hypersensitivity (IH), being serum IgE levels, eosinophil numbers in the bronchoalveolar lavage fluid, and ex vivo IL-4, IL-5, IL-10, IL-13, and IFN-gamma production by the bronchial lymph node cells. BALB/c mice received a combined Diphtheria (D), Tetanus (T), Poliomyelitis, and whole-cell Pertussis vaccine (WCV), a combined D, T, and three-component acellular Pertussis vaccine (ACV), aluminium hydroxide adjuvant, or PBS, 28 and 14 days before B. pertussis infection. Similarly treated non-infected mice were taken as a control. Infection induced pathology; this induction was stronger after (especially WCV) vaccination. WCV but not ACV vaccination induced TNF-alpha expression after challenge. After challenge, IH parameters were strongly increased by (especially ACV) vaccination. Vaccinated IL-4 KO mice showed similar clearance and pathology, in the absence of IgE and with reduced numbers of eosinophils. Vaccinated (Th1-deficient) T-bet KO mice showed reduced clearance and similar pathology. In summary, after challenge vaccination increased lung pathology, TNF-alpha expression (only WCV), and IH parameters. Th1 cells were critical for clearance.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0264-410X
pubmed:author
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2346-60
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:17224216-Administration, Intranasal, pubmed-meshheading:17224216-Animals, pubmed-meshheading:17224216-Bordetella pertussis, pubmed-meshheading:17224216-Diphtheria-Tetanus-Pertussis Vaccine, pubmed-meshheading:17224216-Female, pubmed-meshheading:17224216-Hypersensitivity, Immediate, pubmed-meshheading:17224216-Immunoglobulin E, pubmed-meshheading:17224216-Interferon-gamma, pubmed-meshheading:17224216-Interleukin-10, pubmed-meshheading:17224216-Interleukin-13, pubmed-meshheading:17224216-Interleukin-4, pubmed-meshheading:17224216-Interleukin-5, pubmed-meshheading:17224216-Lung, pubmed-meshheading:17224216-Lymph Nodes, pubmed-meshheading:17224216-Mice, pubmed-meshheading:17224216-Mice, Inbred BALB C, pubmed-meshheading:17224216-Mice, Inbred C57BL, pubmed-meshheading:17224216-Mice, Inbred Strains, pubmed-meshheading:17224216-Mice, Knockout, pubmed-meshheading:17224216-Pertussis Vaccine, pubmed-meshheading:17224216-Tumor Necrosis Factor-alpha, pubmed-meshheading:17224216-Vaccines, Acellular, pubmed-meshheading:17224216-Whooping Cough
pubmed:year
2007
pubmed:articleTitle
Lung pathology and immediate hypersensitivity in a mouse model after vaccination with pertussis vaccines and challenge with Bordetella pertussis.
pubmed:affiliation
Laboratory for Toxicology, Pathology and Genetics, National Institute of Public Health and the Environment, 3720 BA Bilthoven, The Netherlands. r.vandebriel@rivm.nl
pubmed:publicationType
Journal Article