Strange P, Skov L, Baadsgaard O
Department of Dermatology, Gentofte Hospital, University of Copenhagen, Denmark.
J Invest Dermatol. 1994 Feb;102(2):150-4. doi: 10.1111/1523-1747.ep12371753.
During inflammation in the skin keratinocytes can express major histocompatibility complex class II molecules but are unable to present nominal antigens to resting T cells. Certain bacteria including staphylococci produce a new class of antigens termed superantigens that are very potent T-cell activators. Using an in vitro model with cultured normal human keratinocytes and purified allogeneic T cells, we demonstrated that major histocompatibility complex class II+ keratinocytes can activate T cells in the presence of the superantigen staphylococcal enterotoxin B. Major histocompatibility complex class II+ keratinocytes activated T cells at concentrations of staphylococcal enterotoxin B as low as 100 pg/ml. The activation required contact between keratinocytes and T cells, was inhibited with a monoclonal antibody to human leukocyte antigen DR, -DQ, and was not affected by fixation of the keratinocytes. These data show that major histocompatibility complex class II+ keratinocytes activate T cells in the presence of the superantigen staphylococcal enterotoxin B.
在皮肤炎症期间,角质形成细胞可表达主要组织相容性复合体II类分子,但无法将名义抗原呈递给静息T细胞。包括葡萄球菌在内的某些细菌会产生一类新的抗原,称为超抗原,它们是非常有效的T细胞激活剂。利用培养的正常人角质形成细胞和纯化的同种异体T细胞的体外模型,我们证明主要组织相容性复合体II类阳性角质形成细胞在超抗原葡萄球菌肠毒素B存在的情况下可激活T细胞。主要组织相容性复合体II类阳性角质形成细胞在低至100 pg/ml的葡萄球菌肠毒素B浓度下即可激活T细胞。这种激活需要角质形成细胞与T细胞之间的接触,可被抗人白细胞抗原DR、-DQ的单克隆抗体抑制,且不受角质形成细胞固定的影响。这些数据表明,主要组织相容性复合体II类阳性角质形成细胞在超抗原葡萄球菌肠毒素B存在的情况下可激活T细胞。