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Pathogen-Reactive T Helper Cell Analysis in the Pig.

Authors :
Ebner F
Schwiertz P
Steinfelder S
Pieper R
Zentek J
Schütze N
Baums CG
Alber G
Geldhof P
Hartmann S
Source :
Frontiers in immunology [Front Immunol] 2017 May 17; Vol. 8, pp. 565. Date of Electronic Publication: 2017 May 17 (Print Publication: 2017).
Publication Year :
2017

Abstract

There is growing interest in studying host-pathogen interactions in human-relevant large animal models such as the pig. Despite the progress in developing immunological reagents for porcine T cell research, there is an urgent need to directly assess pathogen-specific T cells-an extremely rare population of cells, but of upmost importance in orchestrating the host immune response to a given pathogen. Here, we established that the activation marker CD154 (CD40L), known from human and mouse studies, identifies also porcine antigen-reactive CD4 <superscript>+</superscript> T lymphocytes. CD154 expression was upregulated early after antigen encounter and CD4 <superscript>+</superscript> CD154 <superscript>+</superscript> antigen-reactive T cells coexpressed cytokines. Antigen-induced expansion and autologous restimulation enabled a time- and dose-resolved analysis of CD154 regulation and a significantly increased resolution in phenotypic profiling of antigen-responsive cells. CD154 expression identified T cells responding to staphylococcal Enterotoxin B superantigen stimulation as well as T cells responding to the fungus Candida albicans and T cells specific for a highly prevalent intestinal parasite, the nematode Ascaris suum during acute and trickle infection. Antigen-reactive T cells were further detected after immunization of pigs with a single recombinant bacterial antigen of Streptococcus suis only. Thus, our study offers new ways to study antigen-specific T lymphocytes in the pig and their contribution to host-pathogen interactions.

Details

Language :
English
ISSN :
1664-3224
Volume :
8
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
28567041
Full Text :
https://doi.org/10.3389/fimmu.2017.00565