Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/12755
Title: Molecular properties of human IgG subclasses and their implications for designing therapeutic monoclonal antibodies against infectious diseases.
Authors: Irani, Vashti;Guy, Andrew J;Andrew, Dean;Beeson, James G;Ramsland, Paul A;Richards, Jack S
Affiliation: Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia; Department of Medicine at Royal Melbourne Hospital, University of Melbourne, Parkville, VIC 3050, Australia.
Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia; Department of Immunology, Monash University, Alfred Medical Research and Education Precinct, Melbourne, VIC 3004, Australia.
Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia.
Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia; Department of Medicine at Royal Melbourne Hospital, University of Melbourne, Parkville, VIC 3050, Australia; Department of Microbiology, Monash University, Clayton, VIC 3800, Australia.
Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia; Department of Immunology, Monash University, Alfred Medical Research and Education Precinct, Melbourne, VIC 3004, Australia; Department of Surgery at Austin Health, University of Melbourne, Heidelberg, VIC 3084, Australia; School of Biomedical Sciences, CHIRI Biosciences, Curtin University, Perth, WA 6845, Australia. Electronic address: pramsland@burnet.edu.au.
Centre for Biomedical Research, Burnet Institute, Melbourne, VIC 3004, Australia; Department of Medicine at Royal Melbourne Hospital, University of Melbourne, Parkville, VIC 3050, Australia; Department of Microbiology, Monash University, Clayton, VIC 3800, Australia. Electronic address: richards@burnet.edu.au.
Issue Date: 18-Apr-2015
Citation: Molecular Immunology 2015; 67(2 Pt A): 171-82
Abstract: Monoclonal antibodies are being developed as therapeutics to complement drugs and vaccines or to fill the gap where no drugs or vaccines exist. These therapeutic antibodies (ThAb) may be especially important for infectious diseases in which there is antibiotic resistance, toxin-mediated pathogenesis, or for emerging pathogens. The unique structure of antibodies determines the specific nature of the effector function, so when developing ThAb, the desired effector functions need to be considered and integrated into the design and development processes to ensure maximum efficacy and safety. Antibody subclass is a critical consideration, but it is noteworthy that almost all ThAb that are licenced or currently in development utilise an IgG1 backbone. This review outlines the major structural properties that vary across subclasses, how these properties affect functional immunity, and discusses the various approaches used to study subclass responses to infectious diseases. We also review the factors associated with the selection of antibody subclasses when designing ThAb and highlight circumstances where different subclass properties might be beneficial when applied to particular infectious diseases. These approaches are critical to the future design of ThAb and to the study of naturally-acquired and vaccine-induced immunity.
Internal ID Number: 25900877
URI: http://ahro.austin.org.au/austinjspui/handle/1/12755
DOI: 10.1016/j.molimm.2015.03.255
URL: http://www.ncbi.nlm.nih.gov/pubmed/25900877
Type: Journal Article
Subjects: Antibody-dependent effector mechanisms
IgG subclasses
Infectious diseases
Therapeutic antibodies
Appears in Collections:Journal articles

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