Fujisawa H, Kondo S, Wang B, Shivji G M, Sauder D N
Division of Dermatology, University of Toronto, Ontario, Canada.
Immunology. 1996 Oct;89(2):250-5. doi: 10.1046/j.1365-2567.1996.d01-726.x.
We have previously demonstrated that CD4 gene-targeted mutant mice (CD4- mice) demonstrate hyporesposiveness in contact hypersensitivity (CHS) suggesting that CD4 molecules are required for optimal induction of CHS. In the present study, we wished to examine the mechanisms of this hyporesponsiveness, in particular, we examined whether cytokines were altered in the skin and lymph nodes of CD4- mice following exposure to the contact allergen dinitrofluorobenzene (DNFB). Cytokine mRNA in the ear skin and draining lymph nodes (DLN) were examined by reverse transcription-polymerase chain reaction (RT-PCR) at various times after sensitization. Skin cytokine patterns revealed that in normal mice, interleukin (IL)-2, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha mRNA levels increased at 12 hr sensitization, whereas these cytokines were below the level of detection in CD4- mice. In the DLN of normal mice following the hapten application, sequential upregulation of cytokine mRNA including IL-1 alpha, IL-1 beta, IL-2, IL-4, IL-10, IFN-gamma and TNF-alpha was found. No change was seen for IL-1 alpha, IL-1 beta, IL-10 and TNF-alpha and IL-2, IL-4 and IFN-gamma mRNA levels were below the level of detection in DLN from CD4- mice following the hapten application. However, IL-1 beta, IL-2 and TNF-alpha mRNA levels of lymph node cells from CD4- mice could be upregulated by phorbol myristate acetate in vitro. Flow cytometry study has revealed that the number of Langerhans' cells (LC) in DLN of CD4- mice was similar to that of normal mice, thus, inferring that the alterations of cytokine milieu in the ear skin did not have a significant effect on LC migration to DLN. These results suggest that CD4 molecules are crucial for the induction of certain cytokines in the skin and in inducing sequential cytokine signals in DLN required for optimal development of CHS, but that these changes in cytokines do not effect LC migration.
我们之前已经证明,CD4基因靶向突变小鼠(CD4-小鼠)在接触性超敏反应(CHS)中表现出反应性低下,这表明CD4分子是CHS最佳诱导所必需的。在本研究中,我们希望研究这种反应性低下的机制,特别是,我们检查了接触变应原二硝基氟苯(DNFB)后,CD4-小鼠皮肤和淋巴结中细胞因子是否发生改变。在致敏后的不同时间,通过逆转录-聚合酶链反应(RT-PCR)检测耳皮肤和引流淋巴结(DLN)中的细胞因子mRNA。皮肤细胞因子模式显示,在正常小鼠中,白细胞介素(IL)-2、干扰素(IFN)-γ和肿瘤坏死因子(TNF)-α mRNA水平在致敏12小时时升高,而这些细胞因子在CD4-小鼠中低于检测水平。在正常小鼠的DLN中应用半抗原后,发现包括IL-1α、IL-1β、IL-2、IL-4、IL-10、IFN-γ和TNF-α在内的细胞因子mRNA依次上调。在应用半抗原后,CD4-小鼠的DLN中,IL-1α、IL-1β、IL-10和TNF-α没有变化,IL-2、IL-4和IFN-γ mRNA水平低于检测水平。然而,CD4-小鼠淋巴结细胞的IL-1β、IL-2和TNF-α mRNA水平可在体外被佛波酯肉豆蔻酸酯上调。流式细胞术研究表明,CD4-小鼠DLN中朗格汉斯细胞(LC)的数量与正常小鼠相似,因此,推断耳皮肤中细胞因子环境的改变对LC向DLN的迁移没有显著影响。这些结果表明,CD4分子对于皮肤中某些细胞因子的诱导以及在CHS最佳发展所需的DLN中诱导连续的细胞因子信号至关重要,但这些细胞因子的变化并不影响LC迁移。