Several mutations have been associated with an increased risk of IPF, including those in genes for surfactant proteins (SFTPA2, SFTPC), telomerase reverse transcriptase (TERT), the RNA component of telomerase (TERC), and TOLLIP and MUC5B, all of which play important roles in lung host defense [13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34]. Here, TERT is linked to idiopathic pulmonary fibrosis.