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Publication year
2006Source
Trends in Immunology, 27, 8, (2006), pp. 387-93ISSN
Publication type
Article / Letter to editor
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Organization
Tumorimmunology
Internal Medicine
Journal title
Trends in Immunology
Volume
vol. 27
Issue
iss. 8
Page start
p. 387
Page end
p. 93
Subject
EBP 3: Effective Primary Care and Public Health; N4i 1: Pathogenesis and modulation of inflammation; N4i 2: Invasive mycoses and compromised host; NCMLS 1: Immunity, infection and tissue repair; NCMLS 1: Infection and autoimmunity; NCMLS 2: Immune Regulation; ONCOL 3: Translational research; UMCN 4.1: Microbial pathogenesis and host defenseAbstract
Regulatory T (Treg) cells maintain peripheral tolerance and limit effector responses to prevent excessive immune-mediated tissue damage. However, recent research reveals that Treg cells also dampen the induction of immune responses and, thus, must be controlled to enable the effective protection against infections and cancer. Until now, this control of Treg-cell function has been believed to be by communication through cytokines or by stimulation through co-stimulatory molecules on antigen-presenting cells. However, new evidence has demonstrated that Treg cells can also sense pathogens directly through Toll-like receptors (TLRs) and, consequently, modify their behaviour. This review examines the ramifications of TLR engagement on Treg cells and conventional T cells, and discusses the potential role of TLRs on Treg cells and the consequences for disease therapy.
This item appears in the following Collection(s)
- Academic publications [244228]
- Electronic publications [131195]
- Faculty of Medical Sciences [92893]
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