Cellular immunity in healthy volunteers treated with an octavalent conjugate Pseudomonas aeruginosa vaccine.

Details

Serval ID
serval:BIB_A2BB8B972E45
Type
Article: article from journal or magazin.
Collection
Publications
Title
Cellular immunity in healthy volunteers treated with an octavalent conjugate Pseudomonas aeruginosa vaccine.
Journal
Clinical and experimental immunology
Author(s)
Zuercher A.W., Imboden M.A., Jampen S., Bosse D., Ulrich M., Chtioui H., Lauterburg B.H., Lang A.B.
ISSN
0009-9104 (Print)
ISSN-L
0009-9104
Publication state
Published
Issued date
11/2005
Peer-reviewed
Oui
Volume
142
Number
2
Pages
381-387
Language
english
Notes
Publication types: Clinical Trial, Phase I ; Journal Article
Publication Status: ppublish
Abstract
Humoral immunity in response to an octavalent O-polysaccharide-toxin A conjugate Pseudomonas aeruginosa vaccine is well studied, and a Phase III clinical study in cystic fibrosis (CF) patients is currently ongoing. In contrast, little is known about cellular immunity induced by this vaccine. Fifteen healthy volunteers were immunized on days 1 and 60. Parameters of cellular immunity were studied before vaccination on day 1, and on day 74. Analyses included flow cytometry of whole blood, and antigen-induced proliferation of and cytokine production by lymphocyte cultures. The effects of immunization on the composition of peripheral blood lymphocytes as determined by flow cytometry were minor. In contrast, after immunization a highly significant increase of proliferation in response to stimulation with detoxified toxin A was noted: the stimulation index rose from 1.4 on day 1 to 42.2 on day 74 (restimulation with 0.4 microg/ml; P = 0.003). Immunization led to significant production of interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha by antigen-stimulated lymphocytes. In contrast, no significant induction of interleukin (IL)-4 or IL-10 was observed. In conclusion, immunization of healthy volunteers led to activation of cellular immunity including strong antigen-specific proliferation and cytokine production. In CF patients priming of the cellular immune system towards a Th1-like pattern would be of potential advantage. Therefore, confirmatory analyses in immunized CF patients with and without chronic infection with P. aeruginosa are foreseen.

Keywords
Antibodies, Bacterial/biosynthesis, Bacterial Vaccines/immunology, Cell Proliferation, Cytokines/biosynthesis, Flow Cytometry/methods, Humans, Immunity, Cellular, Immunoglobulin G/biosynthesis, Immunophenotyping/methods, Lymphocyte Activation/immunology, Male, Pseudomonas aeruginosa/immunology, T-Lymphocytes/immunology, Vaccines, Conjugate/immunology
Pubmed
Open Access
Yes
Create date
16/02/2017 13:20
Last modification date
20/08/2019 16:08
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