“…The plausibility of a unique effect of combined Tlr2,4 mutations on T lymphocyte populations was recently demonstrated by Martin et al (39), who showed contact hypersensitivity, a T-cell-mediated inflammatory skin disease, to be abolished in Tlr2,4-/-but not Tlr4-/-mice. In addition, the enhanced lung disease in the Tlr2,4 knockout could involve altered Tlr signaling in B lymphocytes (40,41), a hypothesis supported by our gene expression data, which implicate B cell proliferation and the associated complement response as significant pathways in the radiation-induced pulmonary fibrosis response of B6 mice (18). Furthermore, as Tlr2 and Tlr4 receptors are also expressed on neutrophils (42), and as we have previously shown the numbers of lavage neutrophils to be positively correlated with fibrotic lung disease in a population of genetically mixed mice (8), it is conceivable that defective Tlr signaling in this cell type could affect the level of pulmonary fibrosis.…”