Exosome function: From tumor immunology to pathogen biology

被引:626
作者
Schorey, Jeffrey S. [1 ]
Bhatnagar, Sanchita [1 ]
机构
[1] Univ Notre Dame, Ctr Global Hlth & Infect Dis, Dept Biol Sci, Galvin Life Sci Ctr 130, Notre Dame, IN 46556 USA
关键词
antigens; biomarkers; exosomes; immunity; multivesicular bodies; mycobacteria; vaccine;
D O I
10.1111/j.1600-0854.2008.00734.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Exosomes are the newest family member of 'bioactive vesicles' that function to promote intercellular communication. Exosomes are derived from the fusion of multivesicular bodies with the plasma membrane and extracellular release of the intraluminal vesicles. Recent studies have focused on the biogenesis and composition of exosomes as well as regulation of exosome release. Exosomes have been shown to be released by cells of hematopoietic and non-hematopoietic origin, yet their function remains enigmatic. Much of the prior work has focused on exosomes as a source of tumor antigens and in presentation of tumor antigens to T cells. However, new studies have shown that exosomes might also promote cell-to-cell spread of infectious agents. Moreover, exosomes isolated from cells infected with various intracellular pathogens, including Mycobacterium tuberculosis and Toxoplasma gondii, have been shown to contain microbial components and can promote antigen presentation and macrophage activation, suggesting that exosomes may function in immune surveillance. In this review, we summarize our understanding of exosome biogenesis but focus primarily on new insights into exosome function. We also discuss their possible use as disease biomarkers and vaccine candidates.
引用
收藏
页码:871 / 881
页数:11
相关论文
共 96 条
[1]   Exosomes with major histocompatibility complex class II and co-stimulatory molecules are present in human BAL fluid [J].
Admyre, C ;
Grunewald, J ;
Thyberg, J ;
Gripenbäck, S ;
Tornling, G ;
Eklund, A ;
Scheynius, A ;
Gabrielsson, S .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (04) :578-583
[2]   Toxoplasma gondii antigen-pulsed-dendritic cell-derived exosomes induce a protective immune response against T gondii infection [J].
Aline, F ;
Bout, D ;
Amigorena, S ;
Roingeard, P ;
Dimier-Poisson, I .
INFECTION AND IMMUNITY, 2004, 72 (07) :4127-4137
[3]   TSAP6 facilitates the secretion of translationally controlled tumor protein/histamine-releasing factor via a nonclassical pathway [J].
Amzallag, N ;
Passer, BJ ;
Allanic, D ;
Segura, E ;
Théry, C ;
Goud, B ;
Amson, R ;
Telerman, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :46104-46112
[4]   Exosomes for cancer immunotherapy [J].
Andre, F ;
Escudier, B ;
Angevin, E ;
Tursz, T ;
Zitvogel, L .
ANNALS OF ONCOLOGY, 2004, 15 :141-144
[5]   Tumor-derived exosomes:: a new source of tumor rejection antigens [J].
André, F ;
Scharz, NEC ;
Chaput, N ;
Flament, C ;
Raposo, G ;
Amigorena, S ;
Angevin, E ;
Zitvogel, L .
VACCINE, 2002, 20 :A28-A31
[6]   Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles [J].
Andreola, G ;
Rivoltini, L ;
Castelli, C ;
Huber, V ;
Perego, P ;
Deho, P ;
Squarcina, P ;
Accornero, P ;
Lozupone, F ;
Lugini, L ;
Stringaro, A ;
Molinari, A ;
Arancia, G ;
Gentile, M ;
Parmiani, G ;
Fais, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (10) :1303-1316
[7]   Potent inhibition of macrophage responses to IFN-γ by live virulent Mycobacterium tuberculosis is independent of mature mycobacterial lipoproteins but dependent on TLR2 [J].
Banaiee, Niaz ;
Kincaid, Eleanor Z. ;
Buchwald, Ulrike ;
Jacobs, William R., Jr. ;
Ernst, Joel D. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (05) :3019-3027
[8]   Trafficking and release of mycobacterial lipids from infected macrophages [J].
Beatty, WL ;
Rhoades, ER ;
Ullrich, HJ ;
Chatterjee, D ;
Heuser, JE ;
Russell, DG .
TRAFFIC, 2000, 1 (03) :235-247
[9]   Mycobacterial surface moieties are released from infected macrophages by a constitutive exocytic event [J].
Beatty, WL ;
Ullrich, HJ ;
Russell, DG .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2001, 80 (01) :31-40
[10]   A vaccine based on exosomes secreted by a dendritic cell line confers protection against T. gondii infection in syngeneic and allogeneic mice [J].
Beauvillain, Celine ;
Ruiz, Sophie ;
Guiton, Rachel ;
Bout, Daniel ;
Dimier-Poisson, Isabelle .
MICROBES AND INFECTION, 2007, 9 (14-15) :1614-1622