2017
DOI: 10.4172/2476-1966.1000130
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The Cause of Idiopathic Pulmonary Fibrosis: A Hypothesis

Abstract: Idiopathic pulmonary fibrosis (IPF) is a rapidly fatal condition of unknown cause. The alveolar membrane becomes thickened with collagen and inflammatory and immune cells, which accumulate in the sub-alveolar tissues. The reduction in the ability of oxygen to diffuse across the membrane leads inevitably to progressive anoxia. There is no satisfactory treatment.It is proposed that the histological changes observed in the alveolar membrane are due to an immunological reaction to foreign antigens delivered to the… Show more

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“…When the repair occurs successfully, some type II pneumocytes die while others differentiate into type I pneumocytes. However, under pathological conditions such as idiopathic fibrosis, transforming growth factor beta (TGFβ) mediates the replacement of this process by the proliferation of fibroblasts, which differentiate into myofibroblasts, which secrete collagen and other proteins [7]. The pattern of the inflammatory infiltrate, which was composed mainly by lymphocytes and plasma cells, was probably due to continuous antigenic stimulus that leads to an intense and progressive immune response, especially with regard to light chain immunoglobulins [7].…”
Section: Discussionmentioning
confidence: 99%
“…When the repair occurs successfully, some type II pneumocytes die while others differentiate into type I pneumocytes. However, under pathological conditions such as idiopathic fibrosis, transforming growth factor beta (TGFβ) mediates the replacement of this process by the proliferation of fibroblasts, which differentiate into myofibroblasts, which secrete collagen and other proteins [7]. The pattern of the inflammatory infiltrate, which was composed mainly by lymphocytes and plasma cells, was probably due to continuous antigenic stimulus that leads to an intense and progressive immune response, especially with regard to light chain immunoglobulins [7].…”
Section: Discussionmentioning
confidence: 99%