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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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 |
work_keys_str_mv |
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