Macrophage-Derived Human Resistin Is Induced in Multiple Helminth Infections and Promotes Inflammatory Monocytes and Increased Parasite Burden

被引:41
|
作者
Jang, Jessica C. [1 ]
Chen, Gang [1 ]
Wang, Spencer H. [1 ]
Barnes, Mark A. [1 ]
Chung, Josiah I. [1 ]
Camberis, Mali [2 ]
Le Gros, Graham [2 ]
Cooper, Philip J. [3 ,4 ,5 ]
Steel, Cathy [6 ]
Nutman, Thomas B. [6 ]
Lazar, Mitchell A. [7 ]
Nair, Meera G. [1 ]
机构
[1] Univ Calif Riverside, Div Biomed Sci, Sch Med, Riverside, CA 92521 USA
[2] Malaghan Inst Med Res, Wellington, New Zealand
[3] Lab Invest FEPIS, Quininde, Ecuador
[4] Pontificia Univ Catolica Ecuador, Ctr Invest Enfermedades Infecciosas, Quito, Ecuador
[5] St Georges Univ London, London, England
[6] NIH, Parasit Dis Lab, Bethesda, MD 20892 USA
[7] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
基金
英国惠康基金;
关键词
TOLL-LIKE RECEPTOR; SMOOTH-MUSCLE-CELLS; T-CELL; NEMATODE INFECTION; INSULIN-RESISTANCE; UP-REGULATION; IFN-GAMMA; ACTIVATION; RESPONSES; EXPRESSION;
D O I
10.1371/journal.ppat.1004579
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Parasitic helminth infections can be associated with lifelong morbidity such as immune-mediated organ failure. A better understanding of the host immune response to helminths could provide new avenues to promote parasite clearance and/or alleviate infection-associated morbidity. Murine resistin-like molecules (RELM) exhibit pleiotropic functions following helminth infection including modulating the host immune response; however, the relevance of human RELM proteins in helminth infection is unknown. To examine the function of human resistin (hResistin), we utilized transgenic mice expressing the human resistin gene (hRetnTg(+)). Following infection with the helminth Nippostrongylus brasiliensis (Nb), hResistin expression was significantly upregulated in infected tissue. Compared to control hRetnTg(-) 2 mice, hRetnTg(+) mice suffered from exacerbated Nb-induced inflammation characterized by weight loss and increased infiltration of inflammatory monocytes in the lung, along with elevated Nb egg burdens and delayed parasite expulsion. Genome-wide transcriptional profiling of the infected tissue revealed that hResistin promoted expression of proinflammatory cytokines and genes downstream of toll-like receptor signaling. Moreover, hResistin preferentially bound lung monocytes, and exogenous treatment of mice with recombinant hResistin promoted monocyte recruitment and proinflammatory cytokine expression. In human studies, increased serum resistin was associated with higher parasite load in individuals infected with soil-transmitted helminths or filarial nematode Wuchereria bancrofti, and was positively correlated with proinflammatory cytokines. Together, these studies identify human resistin as a detrimental factor induced by multiple helminth infections, where it promotes proinflammatory cytokines and impedes parasite clearance. Targeting the resistin/proinflammatory cytokine immune axis may provide new diagnostic or treatment strategies for helminth infection and associated immune-mediated pathology.
引用
收藏
页码:1 / 14
页数:14
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