Engineering Therapeutic Monoclonal Antibodies.

Allergy IgE antibody engineering immunology monoclonal antibody therapeutic antibody

Journal

The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002

Informations de publication

Date de publication:
21 Nov 2023
Historique:
received: 11 08 2023
revised: 05 10 2023
accepted: 03 11 2023
medline: 24 11 2023
pubmed: 24 11 2023
entrez: 23 11 2023
Statut: aheadofprint

Résumé

The use of human antibodies as biologic therapeutics has revolutionized patient care throughout fields of medicine. As our understanding of the many roles antibodies play within our natural immune responses continues to advance, so will the number of therapeutic indications for which a monoclonal antibody will be developed. The great breadth of function, long half-life, and modular structure allow for nearly limitless therapeutic possibility. Human antibodies can be rationally engineered to enhance their desired immune functions and eliminate those that may result in unwanted effects. Antibody therapeutics now often start with fully human variable regions, either acquired from genetically engineered humanized mice or from the actual human B cell themselves. These variable genes can be further engineered by widely used methods for optimization of their specificity through affinity maturation, random mutagenesis, targeted mutagenesis, and use of in silico approaches. Antibody isotype selection and deliberate mutations are also used to improve efficacy and tolerability by purposeful fine-tuning of their immune effector functions. Finally, improvements directed at binding to the neonatal Fc receptor can endow therapeutic antibodies with unbelievable extensions in their circulating half-life. The future of engineered antibody therapeutics is bright, with the global monoclonal antibody market projected to exhibit compound annual growth, forecasted to reach a revenue of nearly half a trillion dollars in 2030.

Identifiants

pubmed: 37995859
pii: S0091-6749(23)01476-8
doi: 10.1016/j.jaci.2023.11.018
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Auteurs

Cosby A Stone (CA)

Departments of Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, USA.

Benjamin W Spiller (BW)

Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, USA; Pharmacology, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, USA.

Scott A Smith (SA)

Departments of Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, USA; Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, USA. Electronic address: scott.smith.1@vumc.org.

Classifications MeSH