S. Ardoin, J. Shanahan, and D. Pisetsky, The Role of Microparticles in Inflammation and Thrombosis, Scandinavian Journal of Immunology, vol.95, issue.1, pp.159-65, 2007.
DOI : 10.1046/j.1365-2141.2001.03101.x

B. Hugel, M. Martinez, C. Kunzelmann, and J. Freyssinet, Membrane Microparticles: Two Sides of the Coin, Physiology, vol.20, issue.1, pp.22-29, 2005.
DOI : 10.1152/physiol.00029.2004

A. Leroyer, A. Tedgui, and C. Boulanger, Role of microparticles in atherothrombosis, Journal of Internal Medicine, vol.89, issue.5, pp.528-565, 2008.
DOI : 10.1046/j.1365-2141.2003.04716.x

C. Banfi, M. Brioschi, R. Wait, S. Begum, E. Gianazza et al., Proteome of endothelial cell-derived procoagulant microparticles, PROTEOMICS, vol.101, issue.17, pp.4443-55, 2005.
DOI : 10.1002/pmic.200402017

D. Peterson, T. Sander, S. Kaul, B. Wakim, B. Halligan et al., Comparative proteomic analysis of PAI-1 and TNF-alpha-derived endothelial microparticles, PROTEOMICS, vol.15, issue.12, pp.2430-2476, 2008.
DOI : 10.1002/pmic.200701029

M. Baj-krzyworzeka, R. Szatanek, K. Weglarczyk, J. Baran, B. Urbanowicz et al., Tumour-derived microvesicles carry several surface determinants and mRNA of tumour cells and transfer some of these determinants to monocytes, Cancer Immunology, Immunotherapy, vol.111, issue.7, pp.808-826, 2006.
DOI : 10.1007/s00262-005-0075-9

C. Thery, L. Zitvogel, and S. Amigorena, Exosomes: composition, biogenesis and function, Nat Rev Immunol, vol.2, pp.569-79, 2002.

A. Leroyer, H. Isobe, G. Leseche, Y. Castier, M. Wassef et al., Cellular Origins and Thrombogenic Activity of Microparticles Isolated From Human Atherosclerotic Plaques, Journal of the American College of Cardiology, vol.49, issue.7, pp.772-779, 2007.
DOI : 10.1016/j.jacc.2006.10.053

P. Saas, F. Bonnefoy, S. Kury-paulin, F. Kleinclauss, and S. Perruche, Mediators Involved in the Immunomodulatory Effects of Apoptotic Cells, Transplantation, vol.84, issue.Supplement, pp.31-35, 2007.
DOI : 10.1097/01.tp.0000269113.59857.d6
URL : https://hal.archives-ouvertes.fr/inserm-00479706

B. Koppler, C. Cohen, D. Schlondorff, and M. Mack, Differential mechanisms of microparticle transfer toB cells and monocytes: anti-inflammatory propertiesof microparticles, European Journal of Immunology, vol.106, issue.3, pp.648-60, 2006.
DOI : 10.1002/eji.200535435

M. Martinez, F. Larbret, F. Zobairi, J. Coulombe, N. Debili et al., Transfer of differentiation signal by membrane microvesicles harboring hedgehog morphogens, Blood, vol.108, issue.9, pp.3012-3032, 2006.
DOI : 10.1182/blood-2006-04-019109
URL : https://hal.archives-ouvertes.fr/hal-00105638

D. Sprague, B. Elzey, S. Crist, T. Waldschmidt, R. Jensen et al., Platelet-mediated modulation of adaptive immunity: unique delivery of CD154 signal by platelet-derived membrane vesicles, Blood, vol.111, issue.10, pp.5028-5064, 2008.
DOI : 10.1182/blood-2007-06-097410

A. Mackenzie, H. Wilson, E. Kiss-toth, S. Dower, R. North et al., Rapid Secretion of Interleukin-1?? by Microvesicle Shedding, Immunity, vol.15, issue.5, pp.825-860, 2001.
DOI : 10.1016/S1074-7613(01)00229-1

Z. Mallat, B. Hugel, J. Ohan, G. Leseche, J. Freyssinet et al., Shed Membrane Microparticles With Procoagulant Potential in Human Atherosclerotic Plaques : A Role for Apoptosis in Plaque Thrombogenicity, Circulation, vol.99, issue.3, pp.348-53, 1999.
DOI : 10.1161/01.CIR.99.3.348

N. Amabile, A. Guerin, A. Leroyer, Z. Mallat, C. Nguyen et al., Circulating Endothelial Microparticles Are Associated with Vascular Dysfunction in Patients with End-Stage Renal Failure, Journal of the American Society of Nephrology, vol.16, issue.11, pp.3381-3389, 2005.
DOI : 10.1681/ASN.2005050535

V. Faure, L. Dou, F. Sabatier, C. Cerini, J. Sampol et al., Elevation of circulating endothelial microparticles in patients with chronic renal failure, Journal of Thrombosis and Haemostasis, vol.15, issue.3, pp.566-73, 2006.
DOI : 10.1161/01.ATV.0000141843.77133.fc

F. Sabatier, P. Darmon, B. Hugel, V. Combes, M. Sanmarco et al., Type 1 And Type 2 Diabetic Patients Display Different Patterns of Cellular Microparticles, Diabetes, vol.51, issue.9, pp.2840-2845, 2002.
DOI : 10.2337/diabetes.51.9.2840

V. Pihusch, A. Rank, R. Steber, M. Pihusch, R. Pihusch et al., Endothelial Cell???Derived Microparticles in Allogeneic Hematopoietic Stem Cell Recipients, Transplantation, vol.81, issue.10, pp.1405-1414, 2006.
DOI : 10.1097/01.tp.0000209218.24916.ba

S. Nomura, K. Ishii, N. Inami, Y. Kimura, N. Uoshima et al., Evaluation of Angiopoietins and Cell-Derived Microparticles after Stem Cell Transplantation, Biology of Blood and Marrow Transplantation, vol.14, issue.7, pp.766-74, 2008.
DOI : 10.1016/j.bbmt.2008.04.005

J. Joseph, P. Harrison, I. Mackie, D. Isenberg, and S. Machin, Increased circulating platelet-leucocyte complexes and platelet activation in patients with antiphospholipid syndrome, systemic lupus erythematosus and rheumatoid arthritis, British Journal of Haematology, vol.61, issue.2, pp.451-460, 2001.
DOI : 10.1016/0925-4439(92)90019-J

J. Mcniff and D. Kaplan, Plasmacytoid dendritic cells are present in cutaneous dermatomyositis lesions in a pattern distinct from lupus erythematosus, Journal of Cutaneous Pathology, vol.12, issue.5, pp.452-458, 2008.
DOI : 10.1111/j.1600-0560.2007.00848.x

J. Fonteneau, M. Gilliet, M. Larsson, I. Dasilva, C. Munz et al., Activation of influenza virus-specific CD4+ and CD8+ T cells: a new role for plasmacytoid dendritic cells in adaptive immunity, Blood, vol.101, issue.9, pp.3520-3526, 2003.
DOI : 10.1182/blood-2002-10-3063

M. Gilliet, W. Cao, and Y. Liu, Plasmacytoid dendritic cells: sensing nucleic acids in viral infection and autoimmune diseases, Nature Reviews Immunology, vol.204, issue.8, pp.594-606, 2008.
DOI : 10.1038/nri2358

J. Banchereau and V. Pascual, Type I Interferon in Systemic Lupus Erythematosus and Other Autoimmune Diseases, Immunity, vol.25, issue.3, pp.383-92, 2006.
DOI : 10.1016/j.immuni.2006.08.010

L. Ronnblom and V. Pascual, The innate immune system in SLE: type I interferons and dendritic cells, Lupus, vol.9, issue.5, pp.394-403, 2008.
DOI : 10.1177/0961203308090020

T. Doherty, E. Fisher, and M. Arditi, TLR signaling and trapped vascular dendritic cells in the development of atherosclerosis, Trends in Immunology, vol.27, issue.5, pp.222-229, 2006.
DOI : 10.1016/j.it.2006.03.006

A. Niessner, K. Sato, E. Chaikof, I. Colmegna, J. Goronzy et al., Pathogen-sensing plasmacytoid dendritic cells stimulate cytotoxic Tcell function in the atherosclerotic plaque through interferon-?

A. Niessner, M. Shin, O. Pryshchep, J. Goronzy, E. Chaikof et al., Synergistic Proinflammatory Effects of the Antiviral Cytokine Interferon-?? and Toll-Like Receptor 4 Ligands in the Atherosclerotic Plaque, Circulation, vol.116, issue.18, pp.2043-52, 2007.
DOI : 10.1161/CIRCULATIONAHA.107.697789

M. Gilliet and Y. Liu, Generation of Human CD8 T Regulatory Cells by CD40 Ligand???activated Plasmacytoid Dendritic Cells, The Journal of Experimental Medicine, vol.95, issue.6, pp.695-704, 2002.
DOI : 10.1084/jem.193.2.233

E. Moseman, X. Liang, A. Dawson, A. Panoskaltsis-mortari, A. Krieg et al., Human Plasmacytoid Dendritic Cells Activated by CpG Oligodeoxynucleotides Induce the Generation of CD4+CD25+ Regulatory T Cells, The Journal of Immunology, vol.173, issue.7, pp.4433-4475, 2004.
DOI : 10.4049/jimmunol.173.7.4433

J. Ochando, C. Homma, Y. Yang, A. Hidalgo, A. Garin et al., Alloantigen-presenting plasmacytoid dendritic cells mediate tolerance to vascularized grafts, Nature Immunology, vol.16, issue.6, pp.652-62, 2006.
DOI : 10.1038/ni1333

R. Lande, J. Gregorio, V. Facchinetti, B. Chatterjee, Y. Wang et al., Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide, Nature, vol.7, issue.7162, pp.564-573, 2007.
DOI : 10.1038/nature06116

F. Sabatier, V. Roux, F. Anfosso, L. Camoin, J. Sampol et al., Interaction of endothelial microparticles with monocytic cells in vitro induces tissue factor-dependent procoagulant activity, Blood, vol.99, issue.11, pp.3962-70, 2002.
DOI : 10.1182/blood.V99.11.3962

R. Lacroix, F. Sabatier, A. Mialhe, A. Basire, R. Pannell et al., Activation of plasminogen into plasmin at the surface of endothelial microparticles: a mechanism that modulates angiogenic properties of endothelial progenitor cells in vitro, Blood, vol.110, issue.7, pp.2432-2441, 2007.
DOI : 10.1182/blood-2007-02-069997
URL : https://hal.archives-ouvertes.fr/inserm-00160595

L. Bernal-mizrachi, W. Jy, J. Jimenez, J. Pastor, L. Mauro et al., High levels of circulating endothelial microparticles in patients with acute coronary syndromes, American Heart Journal, vol.145, issue.6, pp.962-70, 2003.
DOI : 10.1016/S0002-8703(03)00103-0

J. Jimenez, W. Jy, L. Mauro, L. Horstman, and Y. Ahn, Elevated endothelial microparticles in thrombotic thrombocytopenic purpura: findings from brain and renal microvascular cell culture and patients with active disease, British Journal of Haematology, vol.260, issue.1, pp.81-90, 2001.
DOI : 10.1016/S0049-3848(98)00151-0

A. Ivanov, Pharmacological Inhibition of Endocytic Pathways: Is It Specific Enough to Be Useful?, Methods Mol Biol, vol.440, pp.15-33, 2008.
DOI : 10.1007/978-1-59745-178-9_2

J. Savill, I. Dransfield, C. Gregory, and C. Haslett, A blast from the past: clearance of apoptotic cells regulates immune responses, Nature Reviews Immunology, vol.22, issue.12, pp.965-75, 2002.
DOI : 10.1038/nri957

S. Wahl, Transforming growth factor-??: innately bipolar, Current Opinion in Immunology, vol.19, issue.1, pp.55-62, 2007.
DOI : 10.1016/j.coi.2006.11.008

G. Penna, S. Sozzani, and L. Adorini, Cutting Edge: Selective Usage of Chemokine Receptors by Plasmacytoid Dendritic Cells, The Journal of Immunology, vol.167, issue.4, pp.1862-1868, 2001.
DOI : 10.4049/jimmunol.167.4.1862

O. Morel, F. Toti, B. Hugel, B. Bakouboula, L. Camoin-jau et al., Procoagulant Microparticles: Disrupting the Vascular Homeostasis Equation?, Arteriosclerosis, Thrombosis, and Vascular Biology, vol.26, issue.12, pp.2594-604, 2006.
DOI : 10.1161/01.ATV.0000246775.14471.26

P. Blanco, A. Palucka, M. Gill, V. Pascual, and J. Banchereau, Induction of Dendritic Cell Differentiation by IFN-alpha in Systemic Lupus Erythematosus, Science, vol.294, issue.5546, pp.1540-1543, 2001.
DOI : 10.1126/science.1064890

V. Pascual, L. Farkas, and J. Banchereau, Systemic lupus erythematosus: all roads lead to type I interferons, Current Opinion in Immunology, vol.18, issue.6, pp.676-82, 2006.
DOI : 10.1016/j.coi.2006.09.014

M. Li, D. Carpio, Y. Zheng, P. Bruzzo, V. Singh et al., An Essential Role of the NF-??B/Toll-Like Receptor Pathway in Induction of Inflammatory and Tissue-Repair Gene Expression by Necrotic Cells, The Journal of Immunology, vol.166, issue.12, pp.7128-7163, 2001.
DOI : 10.4049/jimmunol.166.12.7128

D. Sancho, O. Joffre, A. Keller, N. Rogers, D. Martinez et al., Identification of a dendritic cell receptor that couples sensing of necrosis to immunity, Nature, vol.9, issue.7240, pp.899-903, 2009.
DOI : 10.1038/nature07750

C. Guiducci, G. Ott, J. Chan, E. Damon, C. Calacsan et al., Properties regulating the nature of the plasmacytoid dendritic cell response to Toll-like receptor 9 activation, The Journal of Experimental Medicine, vol.1329, issue.8, pp.1999-2008, 2006.
DOI : 10.4049/jimmunol.174.9.5193

P. Moynagh, TLR signalling and activation of IRFs: revisiting old friends from the NF-??B pathway, Trends in Immunology, vol.26, issue.9, pp.469-76, 2005.
DOI : 10.1016/j.it.2005.06.009

F. Meyer-wentrup, D. Benitez-ribas, P. Tacken, C. Punt, C. Figdor et al., Targeting DCIR on human plasmacytoid dendritic cells results in antigen presentation and inhibits IFN-?? production, Blood, vol.111, issue.8, pp.4245-53, 2008.
DOI : 10.1182/blood-2007-03-081398

F. Garnache-ottou, L. Chaperot, S. Biichle, C. Ferrand, J. Remy-martin et al., Expression of the myeloid-associated marker CD33 is not an exclusive factor for leukemic plasmacytoid dendritic cells, Blood, vol.105, issue.3, pp.1256-64, 2005.
DOI : 10.1182/blood-2004-06-2416
URL : https://hal.archives-ouvertes.fr/hal-00282519