Modulation of the host immune system by phosphorylcholine-containing glycoproteins secreted by parasitic filarial nematodes

被引:71
作者
Harnett, W
Harnett, MM
机构
[1] Univ Strathclyde, Dept Immunol, Todd Ctr, Glasgow G4 0NR, Lanark, Scotland
[2] Univ Glasgow, Dept Immunol, Glasgow G11 6NT, Lanark, Scotland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2001年 / 1539卷 / 1-2期
基金
英国医学研究理事会; 英国惠康基金;
关键词
cytokine; immunomodulation; lymphocyte; nematode; phosphorylcholine; signal transduction;
D O I
10.1016/S0167-4889(01)00101-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phosphorylcholine (PC) is increasingly becoming recognised as a carbohydrate-associated component of a wide variety of procaryotic and eucaryotic pathogens. Studies employing nematode PC-containing molecules indicate that it possesses a plethora of immunomodulatory activities. ES-62 is a PC-containing glycoprotein, which is secreted by the rodent filarial nematode Acanthocheilonema viteae and which provides a model system for the dissection of the mechanisms of immune evasion induced by related PC-containing glycoproteins expressed by human filarial nematodes. At concentrations equivalent to those found for PC-containing molecules in the bloodstream of parasitised humans, ES-62 is able to inhibit antigen receptor-stimulated proliferation of B and T lymphocytes in vitro and in vivo. The active component of ES-62 appears to be PC, as PC conjugated to albumin or even PC alone broadly mimic the results obtained with ES-62. PC-induced impaired lymphocyte responsiveness appears to reflect uncoupling of the antigen receptors from key intracellular proliferative signalling events such as the phosphoinositide 3-kinase, protein kinase C and Pas mitogen-activating protein kinase pathways. Although PC-ES-62 can desensitise B and T cells, not all cells are affected, and in fact it is still possible to generate an antibody response to the molecule. Dissection of this response indicates that it is of the TH-2 type. This appears to reflect the ability of ES-62 to direct the polarity of the T cell response by suppressing the production of proinflammatory cytokines, inducing the induction of anti-inflammatory cytokines and by driving the maturation of dendritic cells that direct TH-2 T cell responses. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
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