Interplay of host-pathogen microvesicles and their role in infectious disease

被引:34
|
作者
Inal, Jameel M. [1 ]
Ansa-Addo, Ephraim A. [2 ]
Lange, Sigrun [3 ]
机构
[1] London Metropolitan Univ, Sch Human Sci, Cellular & Mol Immunol Res Ctr, London N7 8DB, England
[2] Med Univ S Carolina, Dept Immunobiol & Canc Immunol, Hollings Canc Ctr, Charleston, SC 29425 USA
[3] UCL, Inst Womens Hlth, Perinatal Brain Repair Grp, London WC1E 6HX, England
关键词
exosome; infection; intracellular pathogen; microvesicle; CELL-DERIVED MICROVESICLES; LIPID RAFTS; ENTRY; INTERNALIZATION; MICROORGANISMS; CALCIUM; BINDING; EVASION; HIV-1;
D O I
10.1042/BST20120257
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
The release of extracellular vesicles, whether MVs (microvesicles) or exosomes, from host cells or intracellular pathogens is likely to play a significant role in the infection process. Host MVs may fuse with pathogen surfaces to deliver host complement regulatory proteins. They may also deliver cytokines that enhance invasion. Decoy functions are also possible. Whereas host MVs may direct pathogens away from their target cells, pathogen MVs may in turn redirect complement membrane-attack complexes away from their target pathogen. An understanding of the mechanisms of this interplay, bringing about both immune evasion and enhanced invasion, will help to direct future research with a view to rendering pathogens more susceptible to immune attack or in improving drug efficacy. It should also be possible to use MVs or exosomes isolated directly from the pathogens, or from the cells infected with pathogens, to provide alternative vaccination strategies.
引用
收藏
页码:258 / 262
页数:5
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