Correale Jorge, Farez Mauricio
Department of Neurology, Raúl Carrea Institute for Neurological Research (FLENI), Montañeses 2325, Buenos Aires, Argentina.
J Neuroimmunol. 2007 Oct;190(1-2):177-89. doi: 10.1016/j.jneuroim.2007.08.011. Epub 2007 Oct 22.
We investigated whether monocyte-derived dendritic cells (MDDCs) generated in vitro from bacteria-infected MS patients modified autoreactive T cells activation patterns. T cell clones (TCCs) stimulated with MDDCs from infected MS patients responded with maximal proliferation, inducing IL-12, IL-17 and IFN-gamma secretion, at concentrations significantly lower than after incubation with MDDCs isolated from uninfected individuals and bacterial meningitis (BM) patients. Moreover, infected MDDCs promoted TCCs survival, and secreted more IL-12, IL-18, and IL-23. Finally, MDDCs from infected MS subjects showed higher expression of myeloid differentiation factor 88 (MyD88), as well as of HLA-DR, CD1a, CD80, CD86, CD273, CD40, CD83 and CCR7 when compared to MDDCs from uninfected MS individuals, and BM patients. Thus, activation of the innate immune system by microbial products in MS patients affects the generation MDDCs and their ability to modify autoreactive T cell activation patterns, which may be linked to MS relapse induction during bacterial infections.
我们研究了体外从细菌感染的多发性硬化症(MS)患者中产生的单核细胞衍生树突状细胞(MDDC)是否会改变自身反应性T细胞的激活模式。用感染MS患者的MDDC刺激的T细胞克隆(TCC)以最大增殖反应,诱导IL-12、IL-17和IFN-γ分泌,其浓度显著低于与从未感染个体和细菌性脑膜炎(BM)患者分离的MDDC孵育后的浓度。此外,感染的MDDC促进TCC存活,并分泌更多的IL-12、IL-18和IL-23。最后,与未感染MS个体和BM患者的MDDC相比,感染MS受试者的MDDC显示出更高的髓样分化因子88(MyD88)以及HLA-DR、CD1a、CD80、CD86、CD273、CD40、CD83和CCR7表达。因此,MS患者中微生物产物对先天免疫系统的激活会影响MDDC的产生及其改变自身反应性T细胞激活模式的能力,这可能与细菌感染期间MS复发的诱导有关。