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Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2

Rapid progress has been made to identify and study the causative agent leading to coronavirus disease 2019 (COVID‐19) but many questions including who is most susceptible and what determines severity remain unanswered. Angiotensin‐converting enzyme 2 (ACE2) is a key factor in the infection process o...

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Autores principales: Zhu, Hua, Zhang, Hanwen, Zhou, Nina, Ding, Jin, Jiang, Jinquan, Liu, Teli, Liu, Ziyu, Wang, Feng, Zhang, Qian, Zhang, Zhuochen, Yan, Shi, Li, Lei, Benabdallah, Nadia, Jin, Hongjun, Liu, Zhaofei, Cai, Lisheng, Thorek, Daniel L. J., Yang, Xing, Yang, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373167/
https://www.ncbi.nlm.nih.gov/pubmed/34174177
http://dx.doi.org/10.1002/advs.202100965
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author Zhu, Hua
Zhang, Hanwen
Zhou, Nina
Ding, Jin
Jiang, Jinquan
Liu, Teli
Liu, Ziyu
Wang, Feng
Zhang, Qian
Zhang, Zhuochen
Yan, Shi
Li, Lei
Benabdallah, Nadia
Jin, Hongjun
Liu, Zhaofei
Cai, Lisheng
Thorek, Daniel L. J.
Yang, Xing
Yang, Zhi
author_facet Zhu, Hua
Zhang, Hanwen
Zhou, Nina
Ding, Jin
Jiang, Jinquan
Liu, Teli
Liu, Ziyu
Wang, Feng
Zhang, Qian
Zhang, Zhuochen
Yan, Shi
Li, Lei
Benabdallah, Nadia
Jin, Hongjun
Liu, Zhaofei
Cai, Lisheng
Thorek, Daniel L. J.
Yang, Xing
Yang, Zhi
author_sort Zhu, Hua
collection PubMed
description Rapid progress has been made to identify and study the causative agent leading to coronavirus disease 2019 (COVID‐19) but many questions including who is most susceptible and what determines severity remain unanswered. Angiotensin‐converting enzyme 2 (ACE2) is a key factor in the infection process of severe acute respiratory syndrome coronavirus‐2 (SARS‐CoV‐2). In this study, molecularly specific positron emission tomography imaging agents for targeting ACE2 are first developed, and these novel agents are evaluated in vitro, in preclinical model systems, and in a first‐in‐human translational ACE2 imaging of healthy volunteers and a SARS‐CoV‐2 recovered patient (NCT04422457). ACE2 expression levels in different organs in live subjects are quantitatively delineated and observable differences are measured in the patient recovered from COVID‐19. Surprising sites of uptake in the breast, reproductive system and very low uptake in pulmonary tissues are reported. This novel method can add a unique tool to facilitate SARS‐CoV‐2 related research and improve understanding of this enigmatic disease. Molecular imaging provides quantitative annotation of ACE2, the SARS‐CoV‐2 entry receptor, to noninvasively monitor organs impacted by the COVID‐19.
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spelling pubmed-83731672021-08-24 Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2 Zhu, Hua Zhang, Hanwen Zhou, Nina Ding, Jin Jiang, Jinquan Liu, Teli Liu, Ziyu Wang, Feng Zhang, Qian Zhang, Zhuochen Yan, Shi Li, Lei Benabdallah, Nadia Jin, Hongjun Liu, Zhaofei Cai, Lisheng Thorek, Daniel L. J. Yang, Xing Yang, Zhi Adv Sci (Weinh) Research Articles Rapid progress has been made to identify and study the causative agent leading to coronavirus disease 2019 (COVID‐19) but many questions including who is most susceptible and what determines severity remain unanswered. Angiotensin‐converting enzyme 2 (ACE2) is a key factor in the infection process of severe acute respiratory syndrome coronavirus‐2 (SARS‐CoV‐2). In this study, molecularly specific positron emission tomography imaging agents for targeting ACE2 are first developed, and these novel agents are evaluated in vitro, in preclinical model systems, and in a first‐in‐human translational ACE2 imaging of healthy volunteers and a SARS‐CoV‐2 recovered patient (NCT04422457). ACE2 expression levels in different organs in live subjects are quantitatively delineated and observable differences are measured in the patient recovered from COVID‐19. Surprising sites of uptake in the breast, reproductive system and very low uptake in pulmonary tissues are reported. This novel method can add a unique tool to facilitate SARS‐CoV‐2 related research and improve understanding of this enigmatic disease. Molecular imaging provides quantitative annotation of ACE2, the SARS‐CoV‐2 entry receptor, to noninvasively monitor organs impacted by the COVID‐19. John Wiley and Sons Inc. 2021-06-26 /pmc/articles/PMC8373167/ /pubmed/34174177 http://dx.doi.org/10.1002/advs.202100965 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhu, Hua
Zhang, Hanwen
Zhou, Nina
Ding, Jin
Jiang, Jinquan
Liu, Teli
Liu, Ziyu
Wang, Feng
Zhang, Qian
Zhang, Zhuochen
Yan, Shi
Li, Lei
Benabdallah, Nadia
Jin, Hongjun
Liu, Zhaofei
Cai, Lisheng
Thorek, Daniel L. J.
Yang, Xing
Yang, Zhi
Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title_full Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title_fullStr Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title_full_unstemmed Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title_short Molecular PET/CT Profiling of ACE2 Expression In Vivo: Implications for Infection and Outcome from SARS‐CoV‐2
title_sort molecular pet/ct profiling of ace2 expression in vivo: implications for infection and outcome from sars‐cov‐2
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373167/
https://www.ncbi.nlm.nih.gov/pubmed/34174177
http://dx.doi.org/10.1002/advs.202100965
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