Pilström B, Björk L, Böhme J
Department of Immunology, Stockholm University, Sweden.
Cytokine. 1995 Nov;7(8):806-14. doi: 10.1006/cyto.1995.0097.
Cells infiltrating the Langerhans' islets of prediabetic NOD females were isolated from 6 weeks to 6 months of age. These cells were assayed at a single-cell level for production of eight different cytokines by intracellular immunofluorescent staining. By in vitro stimulation with PMA and ionomycin for 4 hours the method is enhanced also to detect in vivo preactivated cells. During the early phase of insulitis from 6 to 12 weeks of age, mainly the monokines IL-1 alpha, IL-6, and TNF were detected. After stimulation, also IFN-gamma and low numbers of IL-10 and GM-CSF producing cells could be observed, but no IL-2 or IL-4 was seen. This cytokine pattern correlates with an increasing insulitis, and we suggest that these cytokines are important in attracting inflammatory cells to the islets, and may cause initial beta-cell destruction. During a later phase, between 4 and 6 months, there is a characteristic TH1 cytokine profile with production of IL-2 and IFN-gamma occurring after stimulation, as well as lymphocytes producing TNF, supposedly TNF-beta. During this period IL-10 was very rarely observed, and no IL-4 production could be found throughout the study. This indicates the absence of a TH2 cytokine profile in this lesion. In addition IL-6 production occurs in high frequencies at all ages, also in endocrine islet cells. We interpret this as a stress response caused by the inflammatory lesion. Our findings show that the effector phase in NOD insulitis is TH1 rather than TH2 mediated. We also demonstrate that cytokines, that may cause initial tissue destruction, are produced during the recruitment of inflammatory cells.
从6周龄至6月龄的糖尿病前期NOD雌性小鼠的胰岛中分离出浸润细胞。通过细胞内免疫荧光染色在单细胞水平上检测这些细胞产生的八种不同细胞因子。通过用佛波酯(PMA)和离子霉素体外刺激4小时,该方法也得到增强,以检测体内预激活的细胞。在6至12周龄的胰岛炎早期,主要检测到单核因子IL-1α、IL-6和TNF。刺激后,还可观察到IFN-γ以及少量产生IL-10和GM-CSF的细胞,但未见到IL-2或IL-4。这种细胞因子模式与胰岛炎的加重相关,我们认为这些细胞因子在吸引炎症细胞至胰岛中起重要作用,并可能导致初始β细胞破坏。在后期,即4至6个月之间,出现特征性的TH1细胞因子谱,刺激后产生IL-2和IFN-γ,以及产生TNF(推测为TNF-β)的淋巴细胞。在此期间,很少观察到IL-10,并且在整个研究中未发现IL-4的产生。这表明该病变中不存在TH2细胞因子谱。此外,IL-6在所有年龄段均高频产生,在内分泌胰岛细胞中也是如此。我们将此解释为炎症病变引起的应激反应。我们的研究结果表明,NOD胰岛炎的效应阶段是由TH1而非TH2介导的。我们还证明,在炎症细胞募集过程中会产生可能导致初始组织破坏的细胞因子。