SARS-CoV-2 antibody magnitude and detectability are driven by disease severity, timing, and assay.
SARS-CoV-2 antibody magnitude and detectability are driven by disease severity, timing, and assay.
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DOI:
10.1126/sciadv.abh3409
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发表时间:
2021-07
期刊:
影响因子:
13.6
通讯作者:
Greenhouse B
中科院分区:
文献类型:
--
作者:
Peluso MJ;Takahashi S;Hakim J;Kelly JD;Torres L;Iyer NS;Turcios K;Janson O;Munter SE;Thanh C;Donatelli J;Nixon CC;Hoh R;Tai V;Fehrman EA;Hernandez Y;Spinelli MA;Gandhi M;Palafox MA;Vallari A;Rodgers MA;Prostko J;Hackett J Jr;Trinh L;Wrin T;Petropoulos CJ;Chiu CY;Norris PJ;DiGermanio C;Stone M;Busch MP;Elledge SK;Zhou XX;Wells JA;Shu A;Kurtz TW;Pak JE;Wu W;Burbelo PD;Cohen JI;Rutishauser RL;Martin JN;Deeks SG;Henrich TJ;Rodriguez-Barraquer I;Greenhouse B
Antibody detection of prior SARS-CoV-2 infection depends on severity, assay, and timing with implications for serosurveillance. Interpretation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serosurveillance studies is limited by poorly defined performance of antibody assays over time in individuals with different clinical presentations. We measured antibody responses in plasma samples from 128 individuals over 160 days using 14 assays. We found a consistent and strong effect of disease severity on antibody magnitude, driven by fever, cough, hospitalization, and oxygen requirement. Responses to spike protein versus nucleocapsid had consistently higher correlation with neutralization. Assays varied substantially in sensitivity during early convalescence and time to seroreversion. Variability was dramatic for individuals with mild infection, who had consistently lower antibody titers, with sensitivities at 6 months ranging from 33 to 98% for commercial assays. Thus, the ability to detect previous infection by SARS-CoV-2 is highly dependent on infection severity, timing, and the assay used. These findings have important implications for the design and interpretation of SARS-CoV-2 serosurveillance studies.
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影响因子:
64.8
作者:
Gaebler C;Wang Z;Lorenzi JCC;Muecksch F;Finkin S;Tokuyama M;Cho A;Jankovic M;Schaefer-Babajew D;Oliveira TY;Cipolla M;Viant C;Barnes CO;Bram Y;Breton G;Hägglöf T;Mendoza P;Hurley A;Turroja M;Gordon K;Millard KG;Ramos V;Schmidt F;Weisblum Y;Jha D;Tankelevich M;Martinez-Delgado G;Yee J;Patel R;Dizon J;Unson-O'Brien C;Shimeliovich I;Robbiani DF;Zhao Z;Gazumyan A;Schwartz RE;Hatziioannou T;Bjorkman PJ;Mehandru S;Bieniasz PD;Caskey M;Nussenzweig MC
通讯作者:
Nussenzweig MC
影响因子:
2
作者:
Zhao, Jijun;Wang, Qin;Zhang, Jianhua
通讯作者:
Zhang, Jianhua
影响因子:
82.9
作者:
Long, Quan-Xin;Liu, Bai-Zhong;Huang, Ai-Long
通讯作者:
Huang, Ai-Long
DOI:
10.1016/s1473-3099(20)30634-4
发表时间:
2020-12
期刊:
The Lancet. Infectious diseases
影响因子:
--
作者:
National SARS-CoV-2 Serology Assay Evaluation Group
通讯作者:
National SARS-CoV-2 Serology Assay Evaluation Group
影响因子:
82.9
作者:
Amanat F;Stadlbauer D;Strohmeier S;Nguyen THO;Chromikova V;McMahon M;Jiang K;Arunkumar GA;Jurczyszak D;Polanco J;Bermudez-Gonzalez M;Kleiner G;Aydillo T;Miorin L;Fierer DS;Lugo LA;Kojic EM;Stoever J;Liu STH;Cunningham-Rundles C;Felgner PL;Moran T;García-Sastre A;Caplivski D;Cheng AC;Kedzierska K;Vapalahti O;Hepojoki JM;Simon V;Krammer F
通讯作者:
Krammer F