Hermansky-Pudlak syndrome: Gene therapy for pulmonary fibrosis

Mol Genet Metab. 2022 Sep-Oct;137(1-2):187-191. doi: 10.1016/j.ymgme.2022.08.008. Epub 2022 Sep 2.

Abstract

Pulmonary fibrosis is a progressive and often fatal lung disease that manifests in most patients with Hermansky-Pudlak syndrome (HPS) type 1. Although the pathobiology of HPS pulmonary fibrosis is unknown, several studies highlight the pathogenic roles of different cell types, including type 2 alveolar epithelial cells, alveolar macrophages, fibroblasts, myofibroblasts, and immune cells. Despite the identification of the HPS1 gene and progress in understanding the pathobiology of HPS pulmonary fibrosis, specific treatment for HPS pulmonary fibrosis is not available, emphasizing the need to identify cellular and molecular targets and to develop therapeutic strategies for this devastating disease. This commentary summarizes recent advances and aims to provide insights into gene therapy for HPS pulmonary fibrosis.

Keywords: Adeno-associated virus; Alveolar type 2 epithelial cell; Gene therapy; Hermansky-Pudlak syndrome; Pulmonary fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Intramural

MeSH terms

  • Genetic Therapy
  • Hermanski-Pudlak Syndrome* / genetics
  • Hermanski-Pudlak Syndrome* / metabolism
  • Hermanski-Pudlak Syndrome* / therapy
  • Humans
  • Lung / pathology
  • Pulmonary Fibrosis* / genetics
  • Pulmonary Fibrosis* / therapy

Supplementary concepts

  • Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells