Therapeutic blockade of CXCR2 rapidly clears inflammation in arthritis and atopic dermatitis models: demonstration with surrogate and humanized antibodies.


Journal

mAbs
ISSN: 1942-0870
Titre abrégé: MAbs
Pays: United States
ID NLM: 101479829

Informations de publication

Date de publication:
Historique:
entrez: 21 12 2020
pubmed: 22 12 2020
medline: 8 10 2021
Statut: ppublish

Résumé

Neutrophils are the most abundant effector cells of the innate immune system and represent the first line of defense against infection. However, in many common pathologies, including autoimmune diseases, excessive recruitment and activation of neutrophils can drive a chronic inflammatory response leading to unwanted tissue destruction. Several strategies have been investigated to tackle pathologic neutrophil biology, and thus provide a novel therapy for chronic inflammatory diseases. The chemokine receptor CXCR2 plays a crucial role in regulating neutrophil homeostasis and is a promising pharmaceutical target. In this study, we report the discovery and validation of a humanized anti-human CXCR2 monoclonal antibody. To enable

Identifiants

pubmed: 33347356
doi: 10.1080/19420862.2020.1856460
pmc: PMC7757791
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
CXCR2 protein, human 0
Receptors, Interleukin-8B 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

1856460

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Auteurs

Md Jahangir Alam (MJ)

Department of Microbiology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

Liang Xie (L)

Department of Microbiology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

Caroline Ang (C)

Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

Farnaz Fahimi (F)

Department of Physiology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

Stephen B Willingham (SB)

Corvus Pharmaceuticals , Burlingame, CA, USA.

Andrew J Kueh (AJ)

Walter and Eliza Hall Institute of Medical Research , Parkville, Victoria, Australia.
Department of Medical Biology, University of Melbourne , Parkville, VIC, Australia.

Marco J Herold (MJ)

Walter and Eliza Hall Institute of Medical Research , Parkville, Victoria, Australia.
Department of Medical Biology, University of Melbourne , Parkville, VIC, Australia.

Charles R Mackay (CR)

Department of Microbiology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

Remy Robert (R)

Department of Physiology, Biomedicine Discovery Institute, Monash University , Clayton, Victoria, Australia.

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Classifications MeSH