Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies

Shiga toxin-producing Escherichia coli (STEC) food contaminations pose serious health concerns, and have been the subject of massive food recalls. STEC has been identified as the major cause of the life-threatening complication of hemolytic uremic syndrome (HUS). Besides supportive care, there curre...

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Main Authors: Larry H. Stanker, Xiaohua He, Stephanie Patfield, Luisa W. Cheng, Thomas D. Henderson
Format: Article
Language:English
Published: MDPI AG 2013-10-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/5/10/1845
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spelling doaj-01a26001600545d98e2188228844399f2020-11-24T22:47:33ZengMDPI AGToxins2072-66512013-10-015101845185810.3390/toxins5101845Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal AntibodiesLarry H. StankerXiaohua HeStephanie PatfieldLuisa W. ChengThomas D. HendersonShiga toxin-producing Escherichia coli (STEC) food contaminations pose serious health concerns, and have been the subject of massive food recalls. STEC has been identified as the major cause of the life-threatening complication of hemolytic uremic syndrome (HUS). Besides supportive care, there currently are no therapeutics available. The use of antibiotics for combating pathogenic E. coli is not recommended because they have been shown to stimulate toxin production. Clearing Stx2 from the circulation could potentially lessen disease severity. In this study, we tested the in vivo neutralization of Stx2 in mice using monoclonal antibodies (mAbs). We measured the biologic half-life of Stx2 in mice and determined the distribution phase or t1/2 α to be 3 min and the clearance phase or t1/2 β to be 40 min. Neutralizing mAbs were capable of clearing Stx2 completely from intoxicated mouse blood within minutes. We also examined the persistence of these mAbs over time and showed that complete protection could be passively conferred to mice 4 weeks before exposure to Stx2. The advent of better diagnositic methods and the availability of a greater arsenal of therapeutic mAbs against Stx2 would greatly enhance treatment outcomes of life threatening E. coli infections.http://www.mdpi.com/2072-6651/5/10/1845monoclonal antibodiesneutralization of Shiga toxinsShiga toxin-producing E. colitoxicokinetics
collection DOAJ
language English
format Article
sources DOAJ
author Larry H. Stanker
Xiaohua He
Stephanie Patfield
Luisa W. Cheng
Thomas D. Henderson
spellingShingle Larry H. Stanker
Xiaohua He
Stephanie Patfield
Luisa W. Cheng
Thomas D. Henderson
Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
Toxins
monoclonal antibodies
neutralization of Shiga toxins
Shiga toxin-producing E. coli
toxicokinetics
author_facet Larry H. Stanker
Xiaohua He
Stephanie Patfield
Luisa W. Cheng
Thomas D. Henderson
author_sort Larry H. Stanker
title Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
title_short Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
title_full Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
title_fullStr Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
title_full_unstemmed Mouse in Vivo Neutralization of Escherichia coli Shiga Toxin 2 with Monoclonal Antibodies
title_sort mouse in vivo neutralization of escherichia coli shiga toxin 2 with monoclonal antibodies
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2013-10-01
description Shiga toxin-producing Escherichia coli (STEC) food contaminations pose serious health concerns, and have been the subject of massive food recalls. STEC has been identified as the major cause of the life-threatening complication of hemolytic uremic syndrome (HUS). Besides supportive care, there currently are no therapeutics available. The use of antibiotics for combating pathogenic E. coli is not recommended because they have been shown to stimulate toxin production. Clearing Stx2 from the circulation could potentially lessen disease severity. In this study, we tested the in vivo neutralization of Stx2 in mice using monoclonal antibodies (mAbs). We measured the biologic half-life of Stx2 in mice and determined the distribution phase or t1/2 α to be 3 min and the clearance phase or t1/2 β to be 40 min. Neutralizing mAbs were capable of clearing Stx2 completely from intoxicated mouse blood within minutes. We also examined the persistence of these mAbs over time and showed that complete protection could be passively conferred to mice 4 weeks before exposure to Stx2. The advent of better diagnositic methods and the availability of a greater arsenal of therapeutic mAbs against Stx2 would greatly enhance treatment outcomes of life threatening E. coli infections.
topic monoclonal antibodies
neutralization of Shiga toxins
Shiga toxin-producing E. coli
toxicokinetics
url http://www.mdpi.com/2072-6651/5/10/1845
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