Schönrich G, Momburg F, Malissen M, Schmitt-Verhulst A M, Malissen B, Hämmerling G J, Arnold B
Institute of Immunology and Genetics, German Cancer Research Center, Heidelberg.
Int Immunol. 1992 May;4(5):581-90. doi: 10.1093/intimm/4.5.581.
Self-reactive T lymphocytes escaping thymic tolerance induction can be rendered non-responsive by contact with antigens in the periphery. In order to determine the parameters controlling peripheral tolerance induction we followed the fate of one well-defined self-reactive T cell population in three different mice expressing the self antigen in various nonlymphoid tissues outside the thymus. This was achieved by crossing anti-Kb T cell receptor (TCR) transgenic mice with transgenic animals expressing the Kb antigen exclusively on hepatocytes or keratinocytes or neuroectodermal cells. Due to this differential expression clonotype+, anti-Kb reactive T cells were found to exist at three different levels of tolerance. These levels were distinct with regard to downregulation of TCR and CD8 molecules, and the requirements for reexpression of TCR in vitro. This differential induction of peripheral tolerance suggest that some tissues are more likely to be affected in autoimmune diseases than others.
逃脱胸腺耐受诱导的自身反应性T淋巴细胞可通过与外周抗原接触而变得无反应。为了确定控制外周耐受诱导的参数,我们追踪了一个定义明确的自身反应性T细胞群体在三种不同小鼠中的命运,这些小鼠在胸腺外的各种非淋巴组织中表达自身抗原。这是通过将抗-Kb T细胞受体(TCR)转基因小鼠与仅在肝细胞、角质形成细胞或神经外胚层细胞上表达Kb抗原的转基因动物杂交来实现的。由于这种差异表达,克隆型阳性、抗-Kb反应性T细胞被发现处于三种不同的耐受水平。这些水平在TCR和CD8分子的下调以及体外TCR重新表达的要求方面是不同的。外周耐受的这种差异诱导表明,在自身免疫性疾病中,某些组织比其他组织更容易受到影响。