The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>

ABSTRACT Monoclonal antibodies (MAbs) have the potential to assist in the battle against multidrug-resistant bacteria such as carbapenem-resistant Klebsiella pneumoniae (CR-Kp). However, the characteristics by which these antibodies (Abs) function, such as the role of antibody subclass, must be dete...

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Autores principales: Michael P. Motley, Elizabeth Diago-Navarro, Kasturi Banerjee, Sean Inzerillo, Bettina C. Fries
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:8a793b86f7f74f27847385216fbb94262021-11-15T16:19:09ZThe Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>10.1128/mBio.02059-202150-7511https://doaj.org/article/8a793b86f7f74f27847385216fbb94262020-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.02059-20https://doaj.org/toc/2150-7511ABSTRACT Monoclonal antibodies (MAbs) have the potential to assist in the battle against multidrug-resistant bacteria such as carbapenem-resistant Klebsiella pneumoniae (CR-Kp). However, the characteristics by which these antibodies (Abs) function, such as the role of antibody subclass, must be determined before such modalities can be carried from the bench to the bedside. We performed a subclass switch on anticapsular monoclonal murine IgG3 (mIgG3) hybridomas and identified and purified a murine IgG1 (mIgG1) hybridoma line through sib selection. We then compared the ability of the mIgG1 and mIgG3 antibodies to control CR-Kp sequence type 258 (ST258) infection both in vitro and in vivo. We found by enzyme-limited immunosorbent assay (ELISA) and flow cytometry that mIgG3 has superior binding to the CR-Kp capsular polysaccharide (CPS) and superior agglutinating ability compared to mIgG1. The mIgG3 also, predictably, had better complement-mediated serum bactericidal activity than the mIgG1 and also promoted neutrophil-mediated killing at concentrations lower than that of the mIgG1. In contrast, the mIgG1 had marginally better activity in improving macrophage-mediated phagocytosis. Comparing their activities in a pulmonary infection model with wild-type as well as neutropenic mice, both antibodies reduced organ burden in a nonlethal challenge, regardless of neutrophil status, with mIgG1 having the highest overall burden reduction in both scenarios. However, at a lethal inoculum, both antibodies showed reduced efficacy in neutropenic mice, with mIgG3 retaining the most activity. These findings suggest the viability of monoclonal Ab adjunctive therapy in neutropenic patients that cannot mount their own immune response, while also providing some insight into the relative contributions of immune mediators in CR-Kp protection. IMPORTANCE Carbapenem-resistant Klebsiella pneumoniae is an urgent public health threat that causes life-threatening infections in immunocompromised hosts. Its resistance to nearly all antibiotics necessitates novel strategies to treat it, including the use of monoclonal antibodies. Monoclonal antibodies are emerging as important adjuncts to traditional pharmaceuticals, and studying how they protect against specific bacteria such as Klebsiella pneumoniae is crucial to their development as effective therapies. Antibody subclass is often overlooked but is a major factor in how an antibody interacts with other mediators of immunity. This paper is the first to examine how the subclass of anticapsular monoclonal antibodies can affect efficacy against CR-Kp. Additionally, this work sheds light on the viability of monoclonal antibody therapy in neutropenic patients, who are most vulnerable to CR-Kp infection.Michael P. MotleyElizabeth Diago-NavarroKasturi BanerjeeSean InzerilloBettina C. FriesAmerican Society for Microbiologyarticleantibody therapymonoclonal antibodiesisotypecarbapenem-resistant Klebsiella pneumoniaeantibiotic resistanceKlebsiellaMicrobiologyQR1-502ENmBio, Vol 11, Iss 5 (2020)
institution DOAJ
collection DOAJ
language EN
topic antibody therapy
monoclonal antibodies
isotype
carbapenem-resistant Klebsiella pneumoniae
antibiotic resistance
Klebsiella
Microbiology
QR1-502
spellingShingle antibody therapy
monoclonal antibodies
isotype
carbapenem-resistant Klebsiella pneumoniae
antibiotic resistance
Klebsiella
Microbiology
QR1-502
Michael P. Motley
Elizabeth Diago-Navarro
Kasturi Banerjee
Sean Inzerillo
Bettina C. Fries
The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
description ABSTRACT Monoclonal antibodies (MAbs) have the potential to assist in the battle against multidrug-resistant bacteria such as carbapenem-resistant Klebsiella pneumoniae (CR-Kp). However, the characteristics by which these antibodies (Abs) function, such as the role of antibody subclass, must be determined before such modalities can be carried from the bench to the bedside. We performed a subclass switch on anticapsular monoclonal murine IgG3 (mIgG3) hybridomas and identified and purified a murine IgG1 (mIgG1) hybridoma line through sib selection. We then compared the ability of the mIgG1 and mIgG3 antibodies to control CR-Kp sequence type 258 (ST258) infection both in vitro and in vivo. We found by enzyme-limited immunosorbent assay (ELISA) and flow cytometry that mIgG3 has superior binding to the CR-Kp capsular polysaccharide (CPS) and superior agglutinating ability compared to mIgG1. The mIgG3 also, predictably, had better complement-mediated serum bactericidal activity than the mIgG1 and also promoted neutrophil-mediated killing at concentrations lower than that of the mIgG1. In contrast, the mIgG1 had marginally better activity in improving macrophage-mediated phagocytosis. Comparing their activities in a pulmonary infection model with wild-type as well as neutropenic mice, both antibodies reduced organ burden in a nonlethal challenge, regardless of neutrophil status, with mIgG1 having the highest overall burden reduction in both scenarios. However, at a lethal inoculum, both antibodies showed reduced efficacy in neutropenic mice, with mIgG3 retaining the most activity. These findings suggest the viability of monoclonal Ab adjunctive therapy in neutropenic patients that cannot mount their own immune response, while also providing some insight into the relative contributions of immune mediators in CR-Kp protection. IMPORTANCE Carbapenem-resistant Klebsiella pneumoniae is an urgent public health threat that causes life-threatening infections in immunocompromised hosts. Its resistance to nearly all antibiotics necessitates novel strategies to treat it, including the use of monoclonal antibodies. Monoclonal antibodies are emerging as important adjuncts to traditional pharmaceuticals, and studying how they protect against specific bacteria such as Klebsiella pneumoniae is crucial to their development as effective therapies. Antibody subclass is often overlooked but is a major factor in how an antibody interacts with other mediators of immunity. This paper is the first to examine how the subclass of anticapsular monoclonal antibodies can affect efficacy against CR-Kp. Additionally, this work sheds light on the viability of monoclonal antibody therapy in neutropenic patients, who are most vulnerable to CR-Kp infection.
format article
author Michael P. Motley
Elizabeth Diago-Navarro
Kasturi Banerjee
Sean Inzerillo
Bettina C. Fries
author_facet Michael P. Motley
Elizabeth Diago-Navarro
Kasturi Banerjee
Sean Inzerillo
Bettina C. Fries
author_sort Michael P. Motley
title The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
title_short The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
title_full The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
title_fullStr The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
title_full_unstemmed The Role of IgG Subclass in Antibody-Mediated Protection against Carbapenem-Resistant <named-content content-type="genus-species">Klebsiella pneumoniae</named-content>
title_sort role of igg subclass in antibody-mediated protection against carbapenem-resistant <named-content content-type="genus-species">klebsiella pneumoniae</named-content>
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/8a793b86f7f74f27847385216fbb9426
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