AI Article Synopsis

  • There is increasing interest in using pigs as models for studying host-pathogen interactions relevant to humans.
  • This study identifies CD154 (CD40L) as a key marker for detecting antigen-reactive CD4 T cells in pigs, crucial for understanding immune responses.
  • The findings demonstrate that T cells can be identified and characterized after exposure to various pathogens, providing new methods for examining immune responses in large animal models.

Article 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 T lymphocytes. CD154 expression was upregulated early after antigen encounter and CD4CD154 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 and T cells specific for a highly prevalent intestinal parasite, the nematode during acute and trickle infection. Antigen-reactive T cells were further detected after immunization of pigs with a single recombinant bacterial antigen of only. Thus, our study offers new ways to study antigen-specific T lymphocytes in the pig and their contribution to host-pathogen interactions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434156PMC
http://dx.doi.org/10.3389/fimmu.2017.00565DOI Listing

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