Harnessing Therapeutic IgE Antibodies to Re-educate Macrophages against Cancer.


Journal

Trends in molecular medicine
ISSN: 1471-499X
Titre abrégé: Trends Mol Med
Pays: England
ID NLM: 100966035

Informations de publication

Date de publication:
06 2020
Historique:
received: 31 10 2019
revised: 05 03 2020
accepted: 09 03 2020
entrez: 30 5 2020
pubmed: 30 5 2020
medline: 9 7 2021
Statut: ppublish

Résumé

Currently, IgG is the only class of antibodies employed for cancer therapy. However, harnessing the unique biological properties of a different class ( e.g., IgE) could engender potent effector cell activation, and unleash previously untapped immune mechanisms against cancer. IgE antibodies are best known for pathogenic roles in allergic diseases and for protective effector functions against parasitic infestation, often mediated by IgE Fc receptor-expressing macrophages. Notably, IgE possess a very high affinity for cognate Fc receptors expressed by tumor-associated macrophages (TAMs). This paper reviews pre-clinical studies, which indicate control of cancer growth by tumor antigen-specific IgE that recruit and re-educate TAMs towards activated profiles. The clinical development harnessing the antitumor potential of recombinant IgE antibodies in cancer patients is also discussed.

Identifiants

pubmed: 32470387
pii: S1471-4914(20)30067-8
doi: 10.1016/j.molmed.2020.03.002
pii:
doi:

Substances chimiques

Antigens, Neoplasm 0
Receptors, Fc 0
Immunoglobulin E 37341-29-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

615-626

Subventions

Organisme : Medical Research Council
ID : MR/L023091/1
Pays : United Kingdom

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Giulia Pellizzari (G)

St. John's Institute of Dermatology, School of Basic and Medical Biosciences, Guy's Hospital, King's College London, London, UK.

Heather J Bax (HJ)

St. John's Institute of Dermatology, School of Basic and Medical Biosciences, Guy's Hospital, King's College London, London, UK; School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Hospital, London, UK.

Debra H Josephs (DH)

St. John's Institute of Dermatology, School of Basic and Medical Biosciences, Guy's Hospital, King's College London, London, UK; School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Hospital, London, UK.

Jelena Gotovina (J)

Institute of Pathophysiology and Allergy Research, Medical University Vienna, Vienna, Austria; The Interuniversity Messerli Research Institute of the University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna, Vienna, Austria.

Erika Jensen-Jarolim (E)

Institute of Pathophysiology and Allergy Research, Medical University Vienna, Vienna, Austria; The Interuniversity Messerli Research Institute of the University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna, Vienna, Austria.

James F Spicer (JF)

School of Cancer and Pharmaceutical Sciences, King's College London, Guy's Hospital, London, UK. Electronic address: james.spicer@kcl.ac.uk.

Sophia N Karagiannis (SN)

St. John's Institute of Dermatology, School of Basic and Medical Biosciences, Guy's Hospital, King's College London, London, UK. Electronic address: sophia.karagiannis@kcl.ac.uk.

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Classifications MeSH