About: Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive

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scientific article published on 07 November 2005

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в лютому 2006 (uk) im November 2005 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en payares de 2005 (ast) scientific article published on 07 November 2005 (en)
publication date	wds:Q64378279-E438A305-5D88-4E14-8EC8-6D6D8E0E98CF
publication date	2005-11-07 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64378279-193AFBE8-0F59-4EFE-AF75-F44624FAD5D6
language of work or name	English
cites work	wds:Q64378279-08A954AE-170C-4E43-8E1B-3EF972F3E286 wds:Q64378279-15EA5413-5F3D-493F-A9B4-7A2879C73ADA wds:Q64378279-1830756A-1163-4B44-9ED0-90A585EF381B wds:Q64378279-1D083527-AF50-4108-9FAA-CC78F6DC7881 wds:Q64378279-1DCE543B-3EDC-4418-A7F8-F8FA02E9E761 wds:Q64378279-2C3DB715-6FF6-46AF-B10D-E710F4AA0AA7 wds:Q64378279-37B1C2F2-4B49-47AA-83EC-31D57FD34995 wds:Q64378279-3C265C9C-C360-4130-B3E3-F63BE7067908 wds:Q64378279-4C984B72-2A20-4241-998D-05F4ACBA4512 wds:Q64378279-767F3CB4-B08C-42BE-B45E-28E9A62A9EDB wds:Q64378279-799E6B67-8FFF-42F1-8302-FA47CB15E975 wds:Q64378279-7B76E74D-F571-447F-B2A3-BE3A22A20086 wds:Q64378279-83D414FC-1462-4555-B0D6-0EE1C5789F5E wds:Q64378279-941E6CA5-13FB-42D0-B4B9-BBCB5F18D22E wds:Q64378279-97DE2EA4-2CB3-4B86-AFC6-7E1B92673FD5 wds:Q64378279-9AAB06F8-FC40-4B66-A2A0-1A0527F7C20B wds:Q64378279-9EC8C91F-2943-439C-B338-56B02357A809 wds:Q64378279-A2DE11ED-3F94-408B-9949-1EABEBE6705C wds:Q64378279-A6D06A5D-28E8-4874-BC7E-A04A8DB0E61E wds:Q64378279-A7E1BE95-5924-4F41-B8AF-11DA8E109C83 wds:Q64378279-B84228F6-7DF8-49C8-B123-8FE6BFDF93B1 wds:Q64378279-B94F0C9C-0A1C-40A0-AFDB-1A0F6126DA8B wds:Q64378279-BEE4AC4F-3AC9-4106-A00A-0D65C872BCC5 wds:Q64378279-CB857799-3A10-4B49-B5B3-53647015B418 wds:Q64378279-CBE7EE80-1B35-42F2-AFF8-163DF19E6C67 wds:Q64378279-D9308FF2-D198-4CAB-85D6-98576541276F wds:Q64378279-DA50B187-B55A-4D17-886E-59F08DEBCC0D wds:Q64378279-DD7AB488-6F4C-4CC9-9DFB-3A4F6DA422F7 wds:Q64378279-DFEB0966-DC47-4A93-BFA9-1ACE6241D90D wds:Q64378279-E5D8916C-40D2-43C9-8C52-8DF7F27A43D9 wds:Q64378279-E91EDD9F-EE5E-4C3B-AF95-4AD6BB470795 wds:Q64378279-F33D0253-0A93-4601-92E8-E4E41CE13F05 wds:Q64378279-F7EC93D2-A5A0-44F9-9F5E-939264F22399
cites work	Eradication of established murine tumors using a novel cell-free vaccine: dendritic cell-derived exosomes Proteomic analysis of dendritic cell-derived exosomes: a secreted subcellular compartment distinct from apoptotic vesicles "Tolerosomes" are produced by intestinal epithelial cells Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles. Endocytosis, intracellular sorting, and processing of exosomes by dendritic cells Direct adenovirus-mediated gene transfer of interleukin 1 and tumor necrosis factor alpha soluble receptors to rabbit knees with experimental arthritis has local and distal anti-arthritic effects Gene therapy for rheumatic diseases Effective treatment of established murine collagen-induced arthritis by systemic administration of dendritic cells genetically modified to express IL-4 Anticytokine treatment of established type II collagen-induced arthritis in DBA/1 mice. A comparative study using anti-TNF alpha, anti-IL-1 alpha/beta, and IL-1Ra Dendritic cells genetically engineered to express IL-4 inhibit murine collagen-induced arthritis Molecules relevant for T cell-target cell interaction are present in cytolytic granules of human T lymphocytes Activated Platelets Release Two Types of Membrane Vesicles: Microvesicles by Surface Shedding and Exosomes Derived From Exocytosis of Multivesicular Bodies and -Granules A phase I study of dexosome immunotherapy in patients with advanced non-small cell lung cancer Induction of specific T-cell tolerance by adenovirus-transfected, Fas ligand-producing antigen presenting cells B lymphocytes secrete antigen-presenting vesicles Molecular characterization of dendritic cell-derived exosomes. Selective accumulation of the heat shock protein hsc73. Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human B-lymphocytes. Effective treatment of established mouse collagen-induced arthritis by systemic administration of dendritic cells genetically modified to express FasL Exosomes derived from IL-10-treated dendritic cells can suppress inflammation and collagen-induced arthritis Intraarticular expression of biologically active interleukin 1-receptor-antagonist protein by ex vivo gene transfer The epithelial cell cytoskeleton and intracellular trafficking. II. Intestinal epithelial cell exosomes: perspectives on their structure and function Viral IL-10 and soluble TNF receptor act synergistically to inhibit collagen-induced arthritis following adenovirus-mediated gene transfer Gene therapy for established murine collagen-induced arthritis by local and systemic adenovirus-mediated delivery of interleukin-4 Dendritic cells genetically engineered to express Fas ligand induce donor-specific hyporesponsiveness and prolong allograft survival Depletion of collagen II-reactive T cells and blocking of B cell activation prevents collagen II-induced arthritis in DBA/1j mice Antigen presenting cells expressing Fas ligand down-modulate chronic inflammatory disease in Fas ligand-deficient mice Viral IL-10 gene transfer inhibits DTH responses to soluble antigens: evidence for involvement of genetically modified dendritic cells and macrophages IL-1 antagonism in inflammatory arthritis Effects of low-dose, noncytotoxic, intraarticular liposomal clodronate on development of erosions and proteoglycan loss in established antigen-induced arthritis in rabbits Pathways to gene therapy in rheumatoid arthritis Direct retrovirus-mediated gene transfer to the synovium of the rabbit knee: implications for arthritis gene therapy Characteristics of plasma membrane isolated from a mouse T lymphoma line: comparison after nitrogen cavitation, shearing, detergent treatment, and microvesiculation
author name string	wds:Q64378279-1F8B0393-1BAE-4FCF-BBBF-0F5D5698D8B1 wds:Q64378279-22F6ADA7-C1CD-4B98-A58A-58DC1B728826 wds:Q64378279-723889BF-D93F-40A1-A445-EB11B4CF79B7 wds:Q64378279-81D1E6F4-14BF-43A3-81B6-0C42439603F5 wds:Q64378279-843DC001-3D6E-4023-BAB2-3DDEF94D30CE wds:Q64378279-A0BC16DE-9803-4B48-8726-5A40A1DEAC39 wds:Q64378279-FF5A08D0-8F6C-4E73-8364-E79DE1169CEC
author name string	Paul D Robbins Rajasree Menon Adrian E Morelli William J Shufesky Eric R Lechman Seon Hee Kim Nicole Bianco
rdfs:label	Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (en) Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (nl)
skos:prefLabel	Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (en) Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (nl)
name	Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (en) Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (nl)
title	wds:Q64378279-68BB6A8B-98CF-4B11-8A78-DF1B5721C1CF
title	Exosomes derived from genetically modified DC expressing FasL are anti-inflammatory and immunosuppressive (en)
page(s)	wds:Q64378279-686585BF-8942-46F9-ACAD-C20B08592DE0

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