Horm Metab Res 2008; 40(2): 82-88
DOI: 10.1055/s-2007-1022548
Review

© Georg Thieme Verlag KG Stuttgart · New York

Exosomes for the Treatment of Human Malignancies

S. Viaud 1 , E. Ullrich 1 , L. Zitvogel 1 , 2 , 3 , N. Chaput 1 , 2
  • 1Institut National de la Santé Et de la Recherche Médicale, INSERM U805, Institut Gustave Roussy, Villejuif, France
  • 2Centre d'investigation Clinique, CIC BT507, Institut Gustave Roussy, Villejuif, France
  • 3Faculté de Médecine Paris Sud, Université Paris XI
Further Information

Publication History

received 22.08.2007

accepted 15.10.2007

Publication Date:
19 February 2008 (online)

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Abstract

Exosomes are nanometer particles (50-100 nm) secreted by most living cells. The first description of exosomes was made in 1987 by Rose Johnstone, who described a vesicle formation during the maturation process of reticulocytes. At this time it has been suggested that exosome release could represent a major route for the externalization of obsolete membrane proteins. A renewed vision of exosome function was raised when Graça Raposo demonstrated in 1996 that exosomes derived from B cells could have immunogenic capacities. Since then, exosomes have been described in numerous cell types in vitro, including hematopoietic and nonhematopoietic cells. The physiological relevance of exosomes in vivo still remains unclear. Studies have demonstrated that exosomes can play a role in the physiology of originating cells (i.e., reticulocyte-derived exosomes). Furthermore, exosomes can act on intercellular communication by allowing exchange of proteins, lipids, and also mRNA between cells. Finally, exosomes have been shown to modulate the immune system (i.e., dendritic cells, B cells, and tumor cells). In the present review, we have focused on the potential therapeutic role of exosomes as a cell free vaccine in cancer.

References

Correspondence

N. ChaputPharm D, PhD 

Centre d'investigation clinique

CIC BT507

Institut Gustave Roussy

39 rue Camille Desmoulins

94805 Villejuif

France

Phone: +33/1/42 11 66 16

Fax: +33/1/42 11 60 94

Email: nathalie.chaput@igr.fr