Abstract
γδ T cells have previously been shown to play a protective role in various animal models of chronic inflammation (e.g., experimental autoimmune encephalomyelitis, collagen-induced arthritis, and non-obese diabetes). This immunoregulatory potential is exerted by synthesizing various anti-inflammatory cytokines and growth factors (e.g., transforming growth factor-β). As the normal balance between inflammatory and regulatory cytokines is perturbed in inflammatory bowel disease (IBD) a protective effect of γδ T cells seems likely. This notion is supported by our finding of increased mortality of rats with 2,4,6-trinitrobenzene sulfonic acid-induced colitis following γδ T cell depletion. In contrast, no effect was observed after depletion of γδ T cells in a Crohn's disease animal model with terminal ileitis (TNFΔARE mice). Therefore, future studies must further define where in the intestinal immune system γδ T cells exert their protective function and how this can be used in the treatment of IBD.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Pathobiology |
| Jahrgang | 70 |
| Ausgabenummer | 3 |
| Seiten (von - bis) | 150-155 |
| Seitenumfang | 6 |
| ISSN | 1015-2008 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 2003 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
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