TY - JOUR
T1 - Peripheral CD4+ T Cell cytokine responses following human challenge and Re-Challenge with campylobacter jejuni
AU - Fimlaid, Kelly A.
AU - Lindow, Janet C.
AU - Tribble, David R.
AU - Bunn, Janice Y.
AU - Maue, Alexander C.
AU - Kirkpatrick, Beth D.
PY - 2014/11/14
Y1 - 2014/11/14
N2 - Campylobacter jejuni is a leading cause of human gastroenteritis worldwide; however, our understanding of the human immune response to C. jejuni infection is limited. A previous human challenge model has shown that C. jejuni elicits IFNc production by peripheral blood mononuclear cells, a response associated with protection from clinical disease following reinfection. In this study, we investigate T lymphocyte profiles associated with campylobacteriosis using specimens from a new human challenge model in which C. jejuni-na?ve subjects were challenged and re-challenged with C. jejuni CG8421. Multiparameter flow cytometry was used to investigate T lymphocytes as a source of cytokines, including IFNc, and to identify cytokine patterns associated with either campylobacteriosis or protection from disease. Unexpectedly, all but one subject evaluated re-experienced campylobacteriosis after re-challenge. We show that CD4+ T cells make IFNγ and other pro-inflammatory cytokines in response to infection; however, multifunctional cytokine response patterns were not found. Cytokine production from peripheral CD4+ T cells was not enhanced following re-challenge, which may suggest deletion or tolerance. Evaluation of alternative paradigms or models is needed to better understand the immune components of protection from campylobacteriosis.
AB - Campylobacter jejuni is a leading cause of human gastroenteritis worldwide; however, our understanding of the human immune response to C. jejuni infection is limited. A previous human challenge model has shown that C. jejuni elicits IFNc production by peripheral blood mononuclear cells, a response associated with protection from clinical disease following reinfection. In this study, we investigate T lymphocyte profiles associated with campylobacteriosis using specimens from a new human challenge model in which C. jejuni-na?ve subjects were challenged and re-challenged with C. jejuni CG8421. Multiparameter flow cytometry was used to investigate T lymphocytes as a source of cytokines, including IFNc, and to identify cytokine patterns associated with either campylobacteriosis or protection from disease. Unexpectedly, all but one subject evaluated re-experienced campylobacteriosis after re-challenge. We show that CD4+ T cells make IFNγ and other pro-inflammatory cytokines in response to infection; however, multifunctional cytokine response patterns were not found. Cytokine production from peripheral CD4+ T cells was not enhanced following re-challenge, which may suggest deletion or tolerance. Evaluation of alternative paradigms or models is needed to better understand the immune components of protection from campylobacteriosis.
UR - http://www.scopus.com/inward/record.url?scp=84911909748&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0112513
DO - 10.1371/journal.pone.0112513
M3 - Article
C2 - 25397604
AN - SCOPUS:84911909748
SN - 1932-6203
VL - 9
JO - PLoS ONE
JF - PLoS ONE
IS - 11
M1 - e112513
ER -