MGH-BIDMC Harvard

Rachel Knipe

Rachel Knipe, MD

Assistant Professor of Medicine

Academic Interests

My research program is focused on defining the pathologic mechanisms which lead from injury to fibrosis in the lung. In particular, I am interested in defining the role of endothelial dysfunction and vascular permeability in the development of pulmonary fibrosis. I have projects looking at the role of endothelial signaling pathways regulated by Rho kinase (ROCK) and Sphingosine-1-phosphate (S1P) in the development of both idiopathic pulmonary fibrosis (IPF) and post-viral pulmonary fibrosis. I am also interested in the development of molecular imaging tools to identify active fibrogenesis using pre-clinical models, with the goal of building novel tools to identify active disease in patients to guide treatment choices by clinicians.

Awards and Recognition

  • Eleanor Shore Fellowship Award (MGH DOM)

  • RCMB Assembly Jo Rae Wright Early Career Investigator Award (ATS)

  • Boehringer Ingelheim Discovery ILD Award

 

A full list of Dr. Knipe’s published work can be found on My Bibliography.

More information can be found on Dr. Knipe's Harvard Catalyst Profile.

 

+Current Projects

  • Role of Vascular Permeability in Pulmonary Fibrosis (K08) This project includes both (1) The role of endothelial ROCK2 in pulmonary fibrosis and (2) The role of endothelial S1PR1 in pulmonary fibrosis
  • Histologic and Transcriptional Profiling of Endothelial Cells During Progressive Pulmonary Fibrosis (R03)
  • Loss of Endothelial S1PR1 Drives Post-Influenza Pulmonary Fibrosis (R01 submitted)
  • Optimization of a PET Allysine Probe to Image Active Fibrogenesis (R33, collaboration with PI Peter Caravan, Martinos Center)