Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Sep;16(9):787-810.
doi: 10.1038/nrd.2017.91. Epub 2017 Jul 14.

Opportunities for therapeutic antibodies directed at G-protein-coupled receptors

Affiliations
Review

Opportunities for therapeutic antibodies directed at G-protein-coupled receptors

Catherine J Hutchings et al. Nat Rev Drug Discov. 2017 Sep.

Erratum in

Abstract

G-protein-coupled receptors (GPCRs) are activated by a diverse range of ligands, from large proteins and proteases to small peptides, metabolites, neurotransmitters and ions. They are expressed on all cells in the body and have key roles in physiology and homeostasis. As such, GPCRs are one of the most important target classes for therapeutic drug discovery. The development of drugs targeting GPCRs has therapeutic value across a wide range of diseases, including cancer, immune and inflammatory disorders as well as neurological and metabolic diseases. The progress made by targeting GPCRs with antibody-based therapeutics, as well as technical hurdles to overcome, are presented and discussed in this Review. Antibody therapeutics targeting C-C chemokine receptor type 4 (CCR4), CCR5 and calcitonin gene-related peptide (CGRP) are used as illustrative clinical case studies.

PubMed Disclaimer

References

    1. Nature. 1996 Nov 14;384(6605):184-7 - PubMed
    1. Intern Emerg Med. 2016 Dec;11(8):1045-1057 - PubMed
    1. Oncotarget. 2016 Jan 19;7(3):2809-22 - PubMed
    1. Sci Rep. 2016 Feb 25;6:21508 - PubMed
    1. Acta Pharmacol Sin. 2012 Mar;33(3):363-71 - PubMed

MeSH terms

Substances

LinkOut - more resources