Acute Respiratory Distress in Aged, SARS-CoV-2-Infected African Green Monkeys but Not Rhesus Macaques.
Acute Respiratory Distress in Aged, SARS-CoV-2-Infected African Green Monkeys but Not Rhesus Macaques.
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感染SARS-CoV-2的老年非洲绿猴的急性呼吸窘迫,但不是恒河猴。
DOI:
10.1016/j.ajpath.2020.10.016
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发表时间:
2021-03
期刊:
影响因子:
--
通讯作者:
Rappaport J
中科院分区:
文献类型:
--
作者:
Blair RV;Vaccari M;Doyle-Meyers LA;Roy CJ;Russell-Lodrigue K;Fahlberg M;Monjure CJ;Beddingfield B;Plante KS;Plante JA;Weaver SC;Qin X;Midkiff CC;Lehmicke G;Golden N;Threeton B;Penney T;Allers C;Barnes MB;Pattison M;Datta PK;Maness NJ;Birnbaum A;Fischer T;Bohm RP;Rappaport J
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a wide range of disease severity, ranging from asymptomatic infection to a life-threating illness, particularly in the elderly population and individuals with comorbid conditions. Among individuals with serious coronavirus 2019 (COVID-19) disease, acute respiratory distress syndrome (ARDS) is a common and often fatal presentation. Animal models of SARS-CoV-2 infection that manifest severe disease are needed to investigate the pathogenesis of COVID-19–induced ARDS and evaluate therapeutic strategies. We report two cases of ARDS in two aged African green monkeys (AGMs) infected with SARS-CoV-2 that had pathological lesions and disease similar to severe COVID-19 in humans. We also report a comparatively mild COVID-19 phenotype characterized by minor clinical, radiographic, and histopathologic changes in the two surviving, aged AGMs and four rhesus macaques (RMs) infected with SARS-CoV-2. Notable increases in circulating cytokines were observed in three of four infected, aged AGMs but not in infected RMs. All the AGMs had increased levels of plasma IL-6 compared with baseline, a predictive marker and presumptive therapeutic target in humans infected with SARS-CoV-2. Together, our results indicate that both RMs and AGMs are capable of modeling SARS-CoV-2 infection and suggest that aged AGMs may be useful for modeling severe disease manifestations, including ARDS.
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影响因子:
64.8
作者:
van Doremalen N;Lambe T;Spencer A;Belij-Rammerstorfer S;Purushotham JN;Port JR;Avanzato VA;Bushmaker T;Flaxman A;Ulaszewska M;Feldmann F;Allen ER;Sharpe H;Schulz J;Holbrook M;Okumura A;Meade-White K;Pérez-Pérez L;Edwards NJ;Wright D;Bissett C;Gilbride C;Williamson BN;Rosenke R;Long D;Ishwarbhai A;Kailath R;Rose L;Morris S;Powers C;Lovaglio J;Hanley PW;Scott D;Saturday G;de Wit E;Gilbert SC;Munster VJ
通讯作者:
Munster VJ
影响因子:
--
作者:
Weiss SR;Leibowitz JL
通讯作者:
Leibowitz JL
影响因子:
168.9
作者:
Huang, Chaolin;Wang, Yeming;Cao, Bin
通讯作者:
Cao, Bin
DOI:
10.1164/ajrccm.163.7.2009111
发表时间:
2001-06-01
影响因子:
24.7
作者:
O'Grady, NP;Preas, HL;Suffredini, AF
通讯作者:
Suffredini, AF
影响因子:
9
作者:
Channappanavar R;Perlman S
通讯作者:
Perlman S