Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection

被引:101
作者
Gaze, Soraya [1 ]
McSorley, Henry J. [1 ]
Daveson, James [2 ]
Jones, Di [2 ]
Bethony, Jeffrey M. [3 ]
Oliveira, Luciana M. [3 ]
Speare, Richard [4 ]
McCarthy, James S. [5 ]
Engwerda, Christian R. [5 ]
Croese, John [6 ]
Loukas, Alex [1 ]
机构
[1] James Cook Univ, Sch Publ Hlth & Trop Med, Cairns, Qld, Australia
[2] Princess Alexandra Hosp, Brisbane, Qld 4102, Australia
[3] George Washington Univ, Washington, DC USA
[4] James Cook Univ, Anton Breinl Ctr, Townsville, Qld 4811, Australia
[5] Queensland Inst Med Res, Brisbane, Qld 4006, Australia
[6] Townsville Hosp, Townsville, Qld, Australia
基金
英国医学研究理事会;
关键词
INFLAMMATORY-BOWEL-DISEASE; DENDRITIC CELL-FUNCTION; NECATOR-AMERICANUS; T-CELLS; MURINE SCHISTOSOMIASIS; CYTOKINE RESPONSES; SECRETED PROTEIN; RETINOIC ACID; INNATE; MICE;
D O I
10.1371/journal.ppat.1002520
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The mucosal cytokine response of healthy humans to parasitic helminths has never been reported. We investigated the systemic and mucosal cytokine responses to hookworm infection in experimentally infected, previously hookworm naive individuals from non-endemic areas. We collected both peripheral blood and duodenal biopsies to assess the systemic immune response, as well as the response at the site of adult worm establishment. Our results show that experimental hookworm infection leads to a strong systemic and mucosal Th2 (IL-4, IL-5, IL-9 and IL-13) and regulatory (IL-10 and TGF-beta) response, with some evidence of a Th1 (IFN-gamma and IL-2) response. Despite upregulation after patency of both IL-15 and ALDH1A2, a known Th17-inducing combination in inflammatory diseases, we saw no evidence of a Th17 (IL-17) response. Moreover, we observed strong suppression of mucosal IL-23 and upregulation of IL-22 during established hookworm infection, suggesting a potential mechanism by which Th17 responses are suppressed, and highlighting the potential that hookworms and their secreted proteins offer as therapeutics for human inflammatory diseases.
引用
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页数:11
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