Yokoi Takashi, Amakawa Ryuichi, Tanijiri Tsutomu, Sugimoto Hiroyuki, Torii Yoshitaro, Amuro Hideki, Son Yonsu, Tajima Kenichirou, Liu Yong-Jun, Ito Tomoki, Fukuhara Shirou
First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
Int Immunol. 2008 Oct;20(10):1321-9. doi: 10.1093/intimm/dxn094. Epub 2008 Aug 13.
Allergic diseases such as atopic dermatitis and asthma develop as a consequence of dysregulated T(h)2 responses. Recently, it has been demonstrated that interaction between dendritic cells (DCs) and thymic stromal lymphopoietin (TSLP), an IL-7-like cytokine, is essential for evoking T(h)2 responses in allergy. In this study, we investigated whether Mycobacterium bovis Bacillus Calmette-Guérin (BCG), a strong T(h)1 response-inducing adjuvant, can alter the function of DCs activated by TSLP (TSLP-DCs). We demonstrated that BCG redirects TSLP-DCs away from inducing inflammatory T(h)2 cells that produce IL-4, IL-5, IL-13 and tumor necrosis factor (TNF)-alpha and toward regulatory T(h)1 cells that produce IFN-gamma and IL-10. We also demonstrated that this functional alteration of TSLP-DCs by BCG depended on both production of IL-12 from DCs and down-regulation of OX40 ligand, a member of the TNF family, on DCs. These findings suggest that BCG might be a useful adjuvant for the treatment of allergic diseases that are triggered by TSLP.
诸如特应性皮炎和哮喘等过敏性疾病是由失调的T(h)2反应引起的。最近,已证明树突状细胞(DC)与胸腺基质淋巴细胞生成素(TSLP,一种白细胞介素-7样细胞因子)之间的相互作用对于在过敏中引发T(h)2反应至关重要。在本研究中,我们调查了牛分枝杆菌卡介苗(BCG),一种诱导强烈T(h)1反应的佐剂,是否能改变由TSLP激活的DC(TSLP-DC)的功能。我们证明,BCG使TSLP-DC从诱导产生白细胞介素-4、白细胞介素-5、白细胞介素-13和肿瘤坏死因子(TNF)-α的炎性T(h)2细胞转向产生干扰素-γ和白细胞介素-10的调节性T(h)1细胞。我们还证明,BCG对TSLP-DC的这种功能改变既依赖于DC产生白细胞介素-12,也依赖于DC上肿瘤坏死因子家族成员OX40配体的下调。这些发现表明,BCG可能是治疗由TSLP引发的过敏性疾病的一种有用佐剂。