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Publication year
2009Source
Blood, 113, 9, (2009), pp. 1977-81ISSN
Publication type
Article / Letter to editor
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Organization
Tumorimmunology
Journal title
Blood
Volume
vol. 113
Issue
iss. 9
Page start
p. 1977
Page end
p. 81
Subject
NCMLS 2: Immune RegulationAbstract
Dendritic cells (DCs) are known to secrete exosomes that transfer membrane proteins, like major histocompatibility complex class II, to other DCs. Intercellular transfer of membrane proteins is also observed during cognate interactions between DCs and CD4(+) T cells. The acquired proteins are functional and play a role in regulation of immune responses. How membrane protein transfer is achieved and regulated is unclear. Here we show that T cells can recruit major histocompatibility complex class II-containing DC exosomes secreted in the extracellular milieu during cognate DC-T-cell interactions. Recruitment of these exosomes required T-cell activation and was dependent on leukocyte function-associated antigen-1 (LFA-1) rather than on T-cell receptor specificity. Indeed, inducing a high-affinity state of LFA-1 on resting T cells was sufficient to provoke exosome binding. These results imply that DC exosomes secreted in the extracellular milieu during cognate T-cell-DC interactions are targeted to T cells activated in that microenvironment.
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- Electronic publications [133894]
- Faculty of Medical Sciences [93266]
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