Paliwal V, Friedman A M, Ptak W, Askenase P W
Department of Medicine, Yale University School of Medicine, New Haven, CT 06510.
J Immunol. 1994 Mar 15;152(6):2811-20.
Contrasuppression is a regulatory T cell activity that acts on helper and contact sensitivity effector T cells to protect them from the action of suppressor T cells. In this study, we examined a monoclonal Ag-specific T cell-secreted contrasuppressor factor (TcsF) with Ag specificity for the hapten TNP (trinitrophenyl). This factor positively influences the adoptive cell transfer of contact sensitivity in the presence of active suppression. Results presented in this report demonstrate a relationship between TcsF and the alpha,beta-T cell receptor (TCR). We found that TcsF bound to mAb anti-TCR-alpha (H28) and to mAb anti-TCR-beta (H57) immunoaffinity columns, but not to a mAb anti-TCR-gamma,delta (UC7) column. The bound contrasuppressor activity could be recovered from these affinity columns by base elution. Reduction of TcsF with DTT followed by alkylation with methylmethanethiosulfonate (MMTS), demonstrated that the active subunit of TcsF bound to and eluted from anti-TCR-alpha, but not to anti-TCR-beta columns. The active TcsF that bound to anti-TCR-alpha but not to the anti-TCR-beta column was shown subsequently to have the ability to bind to specific Ag columns TNP-BSA and TNP-BGG Sepharose 4B. The TcsF could be successfully recovered later from Ag columns; thus suggesting that the Ag-binding domain for mAb, and the biologic activity, resides on the TCR-alpha chain of TcsF. Separation of TcsF on SDS-PAGE under reducing conditions, followed by elution and renaturation of proteins from the gel slices, showed that a 35 to 40 kDa protein had the T cell contrasuppressive activity. Western blot analysis of nonreduced TNP-binding TcsF revealed TCR-alpha,beta determinants on an 80-kDa native molecule similar to TCR-alpha,beta from a helper T cell clone. In summary, Ag-specific, Ag-binding T cell-derived contrasuppressor factor has serologic determinants of TCR-alpha and TCR-beta chains, but the TCR-alpha chain and not the TCR-beta chain is required for biologic function. This TCR-alpha determinant-containing factor is absorbed by specific Ag (TNP) columns. SDS-PAGE analysis under reducing conditions suggested a molecular weight of about 35 to 40 kDa for the TNP-specific TcsF. The mechanism of action of the TCR-alpha-containing contrasuppressor factor in the regulation contact sensitivity is discussed.
抗抑制是一种调节性T细胞活性,作用于辅助性T细胞和接触敏感性效应T细胞,保护它们免受抑制性T细胞的作用。在本研究中,我们检测了一种对三硝基苯(TNP)半抗原具有抗原特异性的单克隆抗原特异性T细胞分泌的抗抑制因子(TcsF)。在存在活性抑制的情况下,该因子对接触敏感性的过继性细胞转移有积极影响。本报告中的结果证明了TcsF与αβ-T细胞受体(TCR)之间的关系。我们发现TcsF能与抗TCR-α单克隆抗体(H28)和抗TCR-β单克隆抗体(H57)免疫亲和柱结合,但不能与抗TCR-γδ单克隆抗体(UC7)柱结合。结合的抗抑制活性可通过碱洗脱从这些亲和柱中回收。用二硫苏糖醇(DTT)还原TcsF,然后用甲硫代磺酸甲酯(MMTS)烷基化,结果表明TcsF的活性亚基与抗TCR-α柱结合并从该柱洗脱,但不与抗TCR-β柱结合。随后显示,与抗TCR-α柱结合而不与抗TCR-β柱结合的活性TcsF能够与特异性抗原柱TNP-BSA和TNP-BGG琼脂糖4B结合。TcsF随后可成功地从抗原柱中回收;因此表明,单克隆抗体的抗原结合域和生物学活性位于TcsF的TCR-α链上。在还原条件下,通过SDS-PAGE分离TcsF,然后从凝胶切片中洗脱并复性蛋白质,结果显示一种35至40 kDa的蛋白质具有T细胞抗抑制活性。对未还原的TNP结合TcsF进行的蛋白质印迹分析显示,在一个80 kDa的天然分子上存在类似于辅助性T细胞克隆的TCR-αβ的决定簇。总之,抗原特异性、抗原结合性的T细胞衍生抗抑制因子具有TCR-α和TCR-β链的血清学决定簇,但生物学功能需要TCR-α链而非TCR-β链。这种含TCR-α决定簇的因子可被特异性抗原(TNP)柱吸附。在还原条件下进行的SDS-PAGE分析表明,TNP特异性TcsF的分子量约为35至40 kDa。本文讨论了含TCR-α的抗抑制因子在调节接触敏感性中的作用机制。