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Pathogen-Reactive T Helper Cell Analysis in the Pig.
- 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