Murzenok Piotr P, Matusevicius Darius, Freedman Mark S
Division of Neurology, Ottawa Hospital General Campus, University of Ottawa, Canada.
Clin Immunol. 2002 Jun;103(3 Pt 1):309-16. doi: 10.1006/clim.2001.5213.
gamma/delta T cells are enriched in multiple sclerosis (MS) brain lesions and have been postulated to contribute to the pathogenesis of the disease. Increased expression of the chemokine receptors CCR5 and CXCR3 on T cells and raised amounts of the chemokines RANTES and IP-10 have been noted in the CSF and brain tissue of MS patients, but the contribution of gamma delta T cells to these increases is unknown. We therefore compared intracellular RANTES and IP-10 production as well as CCR5, CXCR3, and CXCR1 expression by gamma delta T cells derived from the blood and CSF of patients with MS and healthy controls (HC). We observed higher RANTES production by MS gamma delta than by alpha beta T cell lines. Most of the MS as well as the HC gamma delta and alpha beta T cell lines expressed CXCR3, while expression of CXCR1 was low. Interestingly, MS gamma delta T cell lines, compared to lines from HC, expressed lower levels of CCR5. Furthermore, CSF-derived gamma delta T cells had even lower CCR5 expression than blood-derived ones. The higher RANTES production by MS gamma delta T cell lines, together with a lower expression of CCR5, may reflect an autoregulatory loop, caused by an increased production of its ligands (RANTES, MIP-1 alpha, and MIP-1 beta) or due to other pro-inflammatory cytokines. Alternatively, we show that lower CCR5 expression could also reflect the result of repeated in vivo stimulation of gamma delta T cells by autoantigens.
γ/δ T细胞在多发性硬化症(MS)脑损伤中富集,据推测它们在该疾病的发病机制中起作用。在MS患者的脑脊液和脑组织中,已发现T细胞上趋化因子受体CCR5和CXCR3的表达增加,以及趋化因子RANTES和IP-10的含量升高,但γδ T细胞对这些增加的作用尚不清楚。因此,我们比较了来自MS患者和健康对照(HC)血液及脑脊液的γδ T细胞的细胞内RANTES和IP-10产生情况,以及CCR5、CXCR3和CXCR1的表达。我们观察到,MS的γδ T细胞产生的RANTES比αβ T细胞系更多。大多数MS以及HC的γδ和αβ T细胞系表达CXCR3,而CXCR1的表达较低。有趣的是,与HC的细胞系相比,MS的γδ T细胞系表达的CCR5水平较低。此外,脑脊液来源的γδ T细胞的CCR5表达甚至低于血液来源的细胞。MS的γδ T细胞系产生的RANTES较高,同时CCR5表达较低,这可能反映了一种自调节环路,其由配体(RANTES、MIP-1α和MIP-1β)产生增加或其他促炎细胞因子引起。或者,我们表明较低的CCR5表达也可能反映自身抗原对γδ T细胞进行体内反复刺激的结果。