Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice

Obesity is associated with autoimmunity, a phenomenon considered as harmful. Here we show that obese mice and humans produce IgG-type autoantibodies that specifically recognize apolipoprotein B-100 (ApoB100), its native epitope p210, and the synthetic p210 mimotope pB1. By contrast, antibodies again...

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Main Authors: Moon Kyung Choe, Hyung-Ji Kim, Nan Hee Kim, Bert Binas, Hyo Joon Kim
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/14/4/330
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author Moon Kyung Choe
Hyung-Ji Kim
Nan Hee Kim
Bert Binas
Hyo Joon Kim
author_facet Moon Kyung Choe
Hyung-Ji Kim
Nan Hee Kim
Bert Binas
Hyo Joon Kim
author_sort Moon Kyung Choe
collection DOAJ
description Obesity is associated with autoimmunity, a phenomenon considered as harmful. Here we show that obese mice and humans produce IgG-type autoantibodies that specifically recognize apolipoprotein B-100 (ApoB100), its native epitope p210, and the synthetic p210 mimotope pB1. By contrast, antibodies against epitopes p45 and p240, which have been associated with atherosclerosis, were not detected in either the humans or mice. In a longitudinal analysis of high fat diet-fed mice, autoantibody production rose with increasing body weight, then decreased and plateaued at morbid obesity. Likewise, in a cross-sectional analysis of sera from 148 human volunteers spanning a wide BMI range and free of comorbidities, the immunoreactivity increased and then decreased with increasing BMI. Thus, the obesity-related ApoB100-specific natural autoantibodies characteristically showed the same epitope recognition, IgG-type, and biphasic serum levels in humans and mice. We previously reported that a pB1-based vaccine induces similar antibodies and can prevent obesity in mice. Therefore, our present results suggest that autoantibodies directed against native ApoB100 may mitigate obesity, and that the vaccination approach may be effective in humans.
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spelling doaj.art-7fecd46264344e678cef54fa35d316f62023-11-21T14:13:26ZengMDPI AGPharmaceuticals1424-82472021-04-0114433010.3390/ph14040330Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and MiceMoon Kyung Choe0Hyung-Ji Kim1Nan Hee Kim2Bert Binas3Hyo Joon Kim4Department of Molecular & Life Science, College of Science & Technology, Hanyang University (ERICA), 55 Hanyangdaehak-ro, Sangnok-gu, Ansan, Gyeonggi-do 15588, KoreaAsan Medical Center, Department of Neurology, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul 05505, KoreaDepartment of Internal Medicine, Division of Endocrinology and Metabolism, College of Medicine, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, KoreaDepartment of Molecular & Life Science, College of Science & Technology, Hanyang University (ERICA), 55 Hanyangdaehak-ro, Sangnok-gu, Ansan, Gyeonggi-do 15588, KoreaDepartment of Molecular & Life Science, College of Science & Technology, Hanyang University (ERICA), 55 Hanyangdaehak-ro, Sangnok-gu, Ansan, Gyeonggi-do 15588, KoreaObesity is associated with autoimmunity, a phenomenon considered as harmful. Here we show that obese mice and humans produce IgG-type autoantibodies that specifically recognize apolipoprotein B-100 (ApoB100), its native epitope p210, and the synthetic p210 mimotope pB1. By contrast, antibodies against epitopes p45 and p240, which have been associated with atherosclerosis, were not detected in either the humans or mice. In a longitudinal analysis of high fat diet-fed mice, autoantibody production rose with increasing body weight, then decreased and plateaued at morbid obesity. Likewise, in a cross-sectional analysis of sera from 148 human volunteers spanning a wide BMI range and free of comorbidities, the immunoreactivity increased and then decreased with increasing BMI. Thus, the obesity-related ApoB100-specific natural autoantibodies characteristically showed the same epitope recognition, IgG-type, and biphasic serum levels in humans and mice. We previously reported that a pB1-based vaccine induces similar antibodies and can prevent obesity in mice. Therefore, our present results suggest that autoantibodies directed against native ApoB100 may mitigate obesity, and that the vaccination approach may be effective in humans.https://www.mdpi.com/1424-8247/14/4/330obese patientsapolipoprotein B-100IgG-type autoantibodyhigh-fat diet induced obesityepitopemimotope
spellingShingle Moon Kyung Choe
Hyung-Ji Kim
Nan Hee Kim
Bert Binas
Hyo Joon Kim
Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
Pharmaceuticals
obese patients
apolipoprotein B-100
IgG-type autoantibody
high-fat diet induced obesity
epitope
mimotope
title Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
title_full Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
title_fullStr Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
title_full_unstemmed Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
title_short Biphasic Production of Anti-ApoB100 Autoantibodies in Obese Humans and Mice
title_sort biphasic production of anti apob100 autoantibodies in obese humans and mice
topic obese patients
apolipoprotein B-100
IgG-type autoantibody
high-fat diet induced obesity
epitope
mimotope
url https://www.mdpi.com/1424-8247/14/4/330
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