Indirect activation of naïve CD4+ T cells by dendritic cell–derived exosomes
By C. Théry, Livine Duban, É. Segura, P. Véron, O. Lantz, S. Amigorena. Nature Immunology, 2002
960 citations recorded by the source corpus.
Subfields: Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/21f99721f195d7ee43812f11bfc76f129e4148be
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Citations in the corpus
- Extracellular Vesicles: Unique Intercellular Delivery Vehicles. (2017, background): “(B7-1) and CD86 (B7-2) [72] or directly by ICAM-1-presenting mature DC-derived EVs [73].”
- Exosomes: secreted vesicles and intercellular communications (2011, background): “The information transferred could include antigens or MHC–peptide complexes for increasing the range of antigen-presenting cells and the efficiency of induction of immune responses [13-15], or in some cases negative signals leading to death of the target cell [16].”
- The biology and function of exosomes in cancer. (2016, background): “Early studies elucidating the biological functions of exosomes have implicated them in the regulation of adaptive immunity (3, 54).”
- Exosome Secretion: Molecular Mechanisms and Roles in Immune Responses (2011, background): “By contrast, exosomes must be captured by DCs to activate naïve T lymphocytes: these DCs themselves do not necessarily express the right MHC molecules, but can present the exosomal MHC–peptide complexes to specific T cells (46,47).”
- Exosomes: a common pathway for a specialized function. (2006, background): “DC-derived exosomes appear to mediate transfer of MHC class II-peptide complexes to an ‘‘intermediate’’ recipient cell, such as a neighbouring DC, then able to activate CD4+T cells in an antigen specific manner (48).”
- Exosomes are released by cultured cortical neurones. (2006, methodology): “The density and size of these vesicles are compatible with those described for exosomes purified from other cells (Thery et al., 2002a,b).”