Jin Niyun, Taube Christian, Sharp Laura, Hahn Youn-Soo, Yin Xiang, Wands J M, Roark Christina L, O'brien Rebecca L, Gelfand Erwin W, Born Willi K
Department of Immunology, National Jewish Medical and Research Center, Denver, CO 80206, USA.
J Immunol. 2005 Mar 1;174(5):2671-9. doi: 10.4049/jimmunol.174.5.2671.
Gammadelta T cells suppress airway hyperresponsiveness (AHR) induced in allergen-challenged mice but it is not clear whether the suppression is allergen specific. The AHR-suppressive cells express TCR-Vgamma4. To test whether the suppressive function must be induced, we adoptively transferred purified Vgamma4(+) cells into gammadelta T cell-deficient and OVA-sensitized and -challenged recipients (B6.TCR-Vgamma4(-/-)/6(-/-)) and measured the effect on AHR. Vgamma4(+) gammadelta T cells isolated from naive donors were not AHR-suppressive, but Vgamma4(+) cells from OVA-stimulated donors suppressed AHR. Suppressive Vgamma4(+) cells could be isolated from lung and spleen. Their induction in the spleen required sensitization and challenge. In the lung, their function was induced by airway challenge alone. Induction of the suppressors was associated with their activation but it did not alter their ability to accumulate in the lung. Vgamma4(+) gammadelta T cells preferentially express Vdelta4 and -5 but their AHR-suppressive function was not dependent on these Vdeltas. Donor sensitization and challenge not only with OVA but also with two unrelated allergens (ragweed and BSA) induced Vgamma4(+) cells capable of suppressing AHR in the OVA-hyperresponsive recipients, but the process of sensitization and challenge alone (adjuvant and saline only) was not sufficient to induce suppressor function, and LPS as a component of the allergen was not essential. We conclude that AHR-suppressive Vgamma4(+) gammadelta T cells require induction. They are induced by allergen stimulation, but AHR suppression by these cells does not require their restimulation with the same allergen.
γδT细胞可抑制变应原激发的小鼠气道高反应性(AHR),但尚不清楚这种抑制是否具有变应原特异性。具有AHR抑制作用的细胞表达TCR-Vγ4。为了测试这种抑制功能是否必须被诱导,我们将纯化的Vγ4(+)细胞过继转移到γδT细胞缺陷且对卵清蛋白(OVA)致敏并激发的受体(B6.TCR-Vγ4(-/-)/δ(-/-))中,并测量其对AHR的影响。从未接触过抗原的供体中分离出的Vγ4(+)γδT细胞没有AHR抑制作用,但来自OVA刺激供体的Vγ4(+)细胞可抑制AHR。具有抑制作用的Vγ4(+)细胞可从肺和脾中分离得到。它们在脾中的诱导需要致敏和激发。在肺中,其功能仅由气道激发诱导。抑制细胞的诱导与其激活相关,但这并不改变它们在肺中积聚的能力。Vγ4(+)γδT细胞优先表达Vδ4和-5,但其AHR抑制功能并不依赖于这些Vδ。供体不仅用OVA致敏和激发,还用两种无关的变应原(豚草和牛血清白蛋白)致敏和激发,可诱导出能够抑制OVA高反应性受体中AHR的Vγ4(+)细胞,但仅致敏和激发过程(仅用佐剂和生理盐水)不足以诱导抑制功能,且脂多糖作为变应原的组成部分并非必需。我们得出结论,具有AHR抑制作用的Vγ4(+)γδT细胞需要诱导。它们由变应原刺激诱导产生,但这些细胞对AHR的抑制并不需要用相同的变应原再次刺激。