Zanni M P, von Greyerz S, Schnyder B, Mauri-Hellweg D, Brander C, Kalbermatten C, Pichler W J
Institute of Immunology and Allergology, Inselspital, Bern, Switzerland.
Inflamm Res. 1996 Dec;45 Suppl 2:S79-84.
To better understand how T cells react to small compounds, we investigated the in vitro T cell reactivity to drugs from drug allergic patients.
Peripheral blood mononuclear cells (PBMC) of three drug allergic individuals were stimulated in vitro by different drugs.
Proliferation was assayed by 3H-thymidine incorporation. Upregulation of activation parameter on T cells was done by immunofluorescence and cytokine release determined via standard ELISA.
Drugs can stimulate both CD4 and CD8 T-cell subsets. PenG-stimulated PBMC showed a heterogenous cytokine pattern and clones secreted high amounts of INF gamma. In contrast, sulfamethoxazole and lidocaine-stimulated PBMC secreted high levels of IL-5 and lidocaine-specific clones can be Th1 or Th2-like.
Drug specific T cells play a pivotal role in drug hypersensitivity reactions, both by regulating the immune response and probably also as specific effector cells with different patterns of cytokine release.
为了更好地了解T细胞对小分子化合物的反应,我们研究了药物过敏患者的T细胞在体外对药物的反应性。
三名药物过敏个体的外周血单个核细胞(PBMC)在体外被不同药物刺激。
通过3H-胸腺嘧啶核苷掺入法检测增殖。通过免疫荧光检测T细胞上激活参数的上调,并通过标准ELISA测定细胞因子释放。
药物可刺激CD4和CD8 T细胞亚群。青霉素G刺激的PBMC显示出异质性细胞因子模式,克隆分泌大量INFγ。相比之下,磺胺甲恶唑和利多卡因刺激的PBMC分泌高水平的IL-5,利多卡因特异性克隆可以是Th1或Th2样的。
药物特异性T细胞在药物超敏反应中起关键作用,既通过调节免疫反应,也可能作为具有不同细胞因子释放模式的特异性效应细胞。