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Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia

Dyslipidemia is a risk factor for cardiovascular disease (CVD), a major cause of death worldwide. Angiopoietin-like protein 3 (ANGPTL3), recognized as a new therapeutic target for dyslipidemia, regulates the metabolism of low-density lipoprotein-cholesterol (LDL-C) and triglycerides. Here, we design...

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Autores principales: Fukami, Hirotaka, Morinaga, Jun, Nakagami, Hironori, Hayashi, Hiroki, Okadome, Yusuke, Matsunaga, Eiji, Kadomatsu, Tsuyoshi, Horiguchi, Haruki, Sato, Michio, Sugizaki, Taichi, Kuwabara, Takashige, Miyata, Keishi, Mukoyama, Masashi, Morishita, Ryuichi, Oike, Yuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606905/
https://www.ncbi.nlm.nih.gov/pubmed/34841293
http://dx.doi.org/10.1016/j.xcrm.2021.100446
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author Fukami, Hirotaka
Morinaga, Jun
Nakagami, Hironori
Hayashi, Hiroki
Okadome, Yusuke
Matsunaga, Eiji
Kadomatsu, Tsuyoshi
Horiguchi, Haruki
Sato, Michio
Sugizaki, Taichi
Kuwabara, Takashige
Miyata, Keishi
Mukoyama, Masashi
Morishita, Ryuichi
Oike, Yuichi
author_facet Fukami, Hirotaka
Morinaga, Jun
Nakagami, Hironori
Hayashi, Hiroki
Okadome, Yusuke
Matsunaga, Eiji
Kadomatsu, Tsuyoshi
Horiguchi, Haruki
Sato, Michio
Sugizaki, Taichi
Kuwabara, Takashige
Miyata, Keishi
Mukoyama, Masashi
Morishita, Ryuichi
Oike, Yuichi
author_sort Fukami, Hirotaka
collection PubMed
description Dyslipidemia is a risk factor for cardiovascular disease (CVD), a major cause of death worldwide. Angiopoietin-like protein 3 (ANGPTL3), recognized as a new therapeutic target for dyslipidemia, regulates the metabolism of low-density lipoprotein-cholesterol (LDL-C) and triglycerides. Here, we design 3 epitopes (E1-E3) for use in development of a peptide vaccine targeting ANGPTL3 and estimate effects of each on obesity-associated dyslipidemia in B6.Cg-Lep(ob)/J (ob/ob) mice. Vaccination with the E3 ((32)EPKSRFAMLD(41)) peptide significantly reduces circulating levels of triglycerides, LDL-C, and small dense (sd)-LDL-C in ob/ob mice and decreases obese-induced fatty liver. Moreover, E3 vaccination does not induce cytotoxicity in ob/ob mice. Interestingly, the effect of E3 vaccination on dyslipidemia attenuates development of atherosclerosis in B6.KOR/StmSlc-Apoe(shl) mice fed a high-cholesterol diet, which represent a model of severe familial hypercholesterolemia (FH) caused by ApoE loss of function. Taken together, ANGPTL3 vaccination could be an effective therapeutic strategy against dyslipidemia and associated diseases.
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spelling pubmed-86069052021-11-26 Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia Fukami, Hirotaka Morinaga, Jun Nakagami, Hironori Hayashi, Hiroki Okadome, Yusuke Matsunaga, Eiji Kadomatsu, Tsuyoshi Horiguchi, Haruki Sato, Michio Sugizaki, Taichi Kuwabara, Takashige Miyata, Keishi Mukoyama, Masashi Morishita, Ryuichi Oike, Yuichi Cell Rep Med Article Dyslipidemia is a risk factor for cardiovascular disease (CVD), a major cause of death worldwide. Angiopoietin-like protein 3 (ANGPTL3), recognized as a new therapeutic target for dyslipidemia, regulates the metabolism of low-density lipoprotein-cholesterol (LDL-C) and triglycerides. Here, we design 3 epitopes (E1-E3) for use in development of a peptide vaccine targeting ANGPTL3 and estimate effects of each on obesity-associated dyslipidemia in B6.Cg-Lep(ob)/J (ob/ob) mice. Vaccination with the E3 ((32)EPKSRFAMLD(41)) peptide significantly reduces circulating levels of triglycerides, LDL-C, and small dense (sd)-LDL-C in ob/ob mice and decreases obese-induced fatty liver. Moreover, E3 vaccination does not induce cytotoxicity in ob/ob mice. Interestingly, the effect of E3 vaccination on dyslipidemia attenuates development of atherosclerosis in B6.KOR/StmSlc-Apoe(shl) mice fed a high-cholesterol diet, which represent a model of severe familial hypercholesterolemia (FH) caused by ApoE loss of function. Taken together, ANGPTL3 vaccination could be an effective therapeutic strategy against dyslipidemia and associated diseases. Elsevier 2021-11-16 /pmc/articles/PMC8606905/ /pubmed/34841293 http://dx.doi.org/10.1016/j.xcrm.2021.100446 Text en © 2021. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Fukami, Hirotaka
Morinaga, Jun
Nakagami, Hironori
Hayashi, Hiroki
Okadome, Yusuke
Matsunaga, Eiji
Kadomatsu, Tsuyoshi
Horiguchi, Haruki
Sato, Michio
Sugizaki, Taichi
Kuwabara, Takashige
Miyata, Keishi
Mukoyama, Masashi
Morishita, Ryuichi
Oike, Yuichi
Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title_full Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title_fullStr Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title_full_unstemmed Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title_short Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
title_sort vaccine targeting angptl3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606905/
https://www.ncbi.nlm.nih.gov/pubmed/34841293
http://dx.doi.org/10.1016/j.xcrm.2021.100446
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