TY - JOUR
T1 - Molecular PET/CT Profiling of ACE2 Expression In Vivo
T2 - Implications for Infection and Outcome from SARS-CoV-2
AU - Zhu, Hua
AU - Zhang, Hanwen
AU - Zhou, Nina
AU - Ding, Jin
AU - Jiang, Jinquan
AU - Liu, Teli
AU - Liu, Ziyu
AU - Wang, Feng
AU - Zhang, Qian
AU - Zhang, Zhuochen
AU - Yan, Shi
AU - Li, Lei
AU - Benabdallah, Nadia
AU - Jin, Hongjun
AU - Liu, Zhaofei
AU - Cai, Lisheng
AU - Thorek, Daniel L.J.
AU - Yang, Xing
AU - Yang, Zhi
N1 - Funding Information:
This work was supported by National Major Scientific and Technological Special Project for “Significant New Drugs Development” (2017ZX09304021), National Science and Technology Major Project (No. 2020ZX09201023), National Natural Science Foundation (81671733, 81871382, 81871386, 81871387, 21877004, and 92059101), Beijing Municipal Administration of Hospitals‐Yangfan Project (ZYLX201816), Beijing Excellent Talents Funding (2017000021223ZK33), Beijing Millions of Talent Projects A level funding (No. 2019A38), Clinical Medicine Plus X – Young Scholars Project of Peking University (PKU2020LCXQ029). The authors thank Dr. M. Diamond for ACE2‐expressing and control HEK293 cells.
Funding Information:
This work was supported by National Major Scientific and Technological Special Project for ?Significant New Drugs Development? (2017ZX09304021), National Science and Technology Major Project (No. 2020ZX09201023), National Natural Science Foundation (81671733, 81871382, 81871386, 81871387, 21877004, and 92059101), Beijing Municipal Administration of Hospitals-Yangfan Project (ZYLX201816), Beijing Excellent Talents Funding (2017000021223ZK33), Beijing Millions of Talent Projects A level funding (No. 2019A38), Clinical Medicine Plus X ? Young Scholars Project of Peking University (PKU2020LCXQ029). The authors thank Dr. M. Diamond for ACE2-expressing and control HEK293 cells.
Publisher Copyright:
© 2021 The Authors. Advanced Science published by Wiley-VCH GmbH
PY - 2021/8/18
Y1 - 2021/8/18
N2 - 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.
AB - 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.
KW - angiotensin-converting enzyme 2
KW - human
KW - positron emission tomography imaging
KW - severe acute respiratory syndrome coronavirus-2
KW - translational research
UR - http://www.scopus.com/inward/record.url?scp=85108799807&partnerID=8YFLogxK
U2 - 10.1002/advs.202100965
DO - 10.1002/advs.202100965
M3 - Article
C2 - 34174177
AN - SCOPUS:85108799807
SN - 2198-3844
VL - 8
JO - Advanced Science
JF - Advanced Science
IS - 16
M1 - 2100965
ER -