An anti-CRF antibody suppresses the HPA axis and reverses stress-induced phenotypes

J Exp Med. 2019 Nov 4;216(11):2479-2491. doi: 10.1084/jem.20190430. Epub 2019 Aug 29.

Abstract

Hypothalamic-pituitary-adrenal (HPA) axis dysfunction contributes to numerous human diseases and disorders. We developed a high-affinity monoclonal antibody, CTRND05, targeting corticotropin-releasing factor (CRF). In mice, CTRND05 blocks stress-induced corticosterone increases, counteracts effects of chronic variable stress, and induces other phenotypes consistent with suppression of the HPA axis. CTRND05 induces skeletal muscle hypertrophy and increases lean body mass, effects not previously reported with small-molecule HPA-targeting pharmacologic agents. Multiorgan transcriptomics demonstrates broad HPA axis target engagement through altering levels of known HPA-responsive transcripts such as Fkbp5 and Myostatin and reveals novel HPA-responsive pathways such as the Apelin-Apelin receptor system. These studies demonstrate the therapeutic potential of CTRND05 as a suppressor of the HPA axis and serve as an exemplar of a potentially broader approach to target neuropeptides with immunotherapies, as both pharmacologic tools and novel therapeutics.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology*
  • Cell Line, Tumor
  • Corticosterone / immunology
  • Corticosterone / metabolism
  • Corticotropin-Releasing Hormone / antagonists & inhibitors*
  • Corticotropin-Releasing Hormone / immunology
  • Gene Expression Profiling / methods
  • Humans
  • Hypothalamo-Hypophyseal System / drug effects*
  • Hypothalamo-Hypophyseal System / immunology
  • Hypothalamo-Hypophyseal System / metabolism
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Phenotype
  • Pituitary-Adrenal System / drug effects*
  • Pituitary-Adrenal System / immunology
  • Pituitary-Adrenal System / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Stress, Physiological / drug effects*
  • Stress, Physiological / immunology

Substances

  • Antibodies, Monoclonal
  • Corticotropin-Releasing Hormone
  • Corticosterone