Renz H, Bradley K, Saloga J, Loader J, Larsen G L, Gelfand E W
Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
J Exp Med. 1993 Apr 1;177(4):1175-80. doi: 10.1084/jem.177.4.1175.
The role of T cells expressing specific V beta elements was examined in the regulation of allergen-specific immunoglobulin (Ig)E production and airways responsiveness (AR). In BALB/c mice, inhalation of the allergen ovalbumin (OVA) induced an IgE anti-OVA response, immediate cutaneous reactivity, and increased AR. These results were associated with an expansion of V beta 8.1/8.2 T cells in local draining lymph nodes of the airways and the lung. Transfer of V beta 8.1/8.2 T cells from sensitized mice stimulated an IgE anti-OVA response, immediate cutaneous hypersensitivity, and increased AR in naive syngeneic recipients. In contrast, OVA-reactive V beta 2 T cells inhibited these effects. These data demonstrate for the first time that T cells with different V beta specificities play a critical role in the in vivo regulation of allergen-specific IgE production and AR.
表达特定Vβ元件的T细胞在变应原特异性免疫球蛋白(Ig)E产生和气道反应性(AR)的调节中的作用进行了研究。在BALB/c小鼠中,吸入变应原卵清蛋白(OVA)诱导了IgE抗OVA反应、即刻皮肤反应性,并增加了AR。这些结果与气道和肺部局部引流淋巴结中Vβ8.1/8.2 T细胞的扩增有关。来自致敏小鼠的Vβ8.1/8.2 T细胞的转移刺激了同基因未致敏受体中的IgE抗OVA反应、即刻皮肤超敏反应,并增加了AR。相反,OVA反应性Vβ2 T细胞抑制了这些效应。这些数据首次证明,具有不同Vβ特异性的T细胞在变应原特异性IgE产生和AR的体内调节中起关键作用。