Department of Dermatology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
J Clin Invest. 2011 Oct;121(10):3860-71. doi: 10.1172/JCI45963. Epub 2011 Sep 1.
It is well established that allergy development can be prevented by repeated low-dose exposure to contact allergens. Exactly which immune mechanisms are responsible for this so-called low zone tolerance (LZT) is not clear, although CD8⁺ suppressor T cells are known to have a role. Here, we show that TNF released by tolerogenic CD11⁺CD8⁺ DCs located in skin-draining lymph nodes is required and sufficient for development of tolerance to contact allergens in mice. DC-derived TNF protected mice from contact allergy by inducing apoptosis in allergen-specific effector CD8⁺ T cells via TNF receptor 2 but did not contribute to the generation and function of the regulatory T cells associated with LZT. The TNF-mediated killing mechanism was induced in an allergen-specific manner. Activation of tolerogenic DCs by LZT CD8⁺ suppressor T cells and enhanced TNF receptor 2 expression on contact allergen-specific CD8⁺ effector T cells were required for LZT. Our findings may explain how tolerance protects from allergic diseases, which could allow for the development of new strategies for allergy prevention.
众所周知,通过反复接触低剂量的变应原,可以预防过敏的发生。虽然已知 CD8+抑制性 T 细胞在其中发挥作用,但对于导致这种所谓的低区耐受(LZT)的确切免疫机制尚不清楚。在这里,我们发现位于皮肤引流淋巴结中的耐受型 CD11+CD8+DC 释放的 TNF 对于在小鼠中诱导接触变应原的耐受性是必需且充分的。DC 衍生的 TNF 通过 TNF 受体 2 诱导过敏原特异性效应 CD8+T 细胞凋亡,从而保护小鼠免受接触过敏,但对与 LZT 相关的调节性 T 细胞的产生和功能没有贡献。TNF 介导的杀伤机制以过敏原特异性方式诱导。LZT CD8+抑制性 T 细胞激活耐受型 DC 并增强接触变应原特异性 CD8+效应 T 细胞上的 TNF 受体 2 的表达,这对于 LZT 是必需的。我们的发现可以解释为什么耐受可以预防过敏疾病,这可能为过敏预防的新策略的发展提供了依据。