SENSITIVITY TO BLEOMYCIN-INDUCED LUNG INJURY IS NOT MODERATED BY AN ANTIGEN-LIMITED T-CELL REPERTOIRE

Abstract

Pulmonary fibrosis is a progressive scarring disease of the lung. It has been suggested that fibrosis is an inflammatory process, and cytokines such as tumor necrosis factor (TNF)-α and transforming growth factor (TGF)-β have been shown to play key roles in the pathogenesis of fibrotic lung disease. However, the source of these cytokines remains in question and there is controversy over the role that infiltrating inflammatory cells play in fibrosis. T cells could play a key role by releasing cytokines upon engaging autoantigens revealed as a result of necrosis or apoptosis following epithelial injury. Some studies have shown that disrupting T-cell function leads to more severe disease, whereas others have shown that T-cell deficiency protects against fibrotic injury. To investigate whether specific antigen engagement by T cells is required for the development of fibrosis, bleomycin was instilled into the lungs of mice expressing a transgenic T-cell receptor β (TCRβ) gene. Expression of the TCRβ transgene prevents effective recognition of antigens other than a single epitope of hen egg lysozyme. These mice therefore have defective antigen-specific responses but a normal representation of mature T-cell subsets. If antigen-specific T-cell engagement is required for the development of lung fibrosis, bleomycin-induced fibrosis should be reduced in the TCRβ transgenic mice. In fact, there is no difference in the inflammatory or fibrotic response to bleomycin between TCRβ transgenic and control mice. Thus, if T cells are required for fibrogenesis, it must involve an antigen-independent mechanism.

Keywords:

• bleomycin
• fibrosis
• T cells
• T-cell repertoire
• alpha smooth muscle actin
• myofibroblasts