Early detection of neutralizing antibodies against SARS-CoV-2 in COVID-19 patients in Thailand.
Early detection of neutralizing antibodies against SARS-CoV-2 in COVID-19 patients in Thailand.
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DOI:
10.1371/journal.pone.0246864
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发表时间:
2021
期刊:
影响因子:
3.7
通讯作者:
Hemachudha T
中科院分区:
文献类型:
--
作者:
Putcharoen O;Wacharapluesadee S;Chia WN;Paitoonpong L;Tan CW;Suwanpimolkul G;Jantarabenjakul W;Ruchisrisarod C;Wanthong P;Sophonphan J;Chariyavilaskul P;Wang LF;Hemachudha T
The presence of neutralizing antibodies (NAbs) is an indicator of protective immunity for most viral infections. A newly developed surrogate viral neutralization assay (sVNT) offers the ability to detect total receptor binding domain-targeting NAbs in an isotype-independent manner, increasing the test sensitivity. Thus, specimens with low IgM/ IgG antibody levels showed strong neutralization activity in sVNT. This study aimed to measure the %inhibition of NAbs measured by sVNT in PCR-confirmed COVID-19 patients. The sensitivity of sVNT for the diagnosis of SARS-CoV-2 infection and its kinetics were determined. Ninety-seven patients with PCR-confirmed SARS-CoV-2 infection were included in this study. Majority of the patients were 21–40 years old (67%) and 63% had mild symptoms. The sensitivity of sVNT for the diagnosis of SARS-CoV-2 infection was 99% (95% confidence interval (CI) 94.4–100%) and the specificity was 100% (95% CI 98.3–100%). The negative predictive value of sVNT from the samples collected before and after 7 days of symptom onset was 99.5% (95% CI 97.4–100%) and 100% (95% CI 93.8–100%), respectively. The level of inhibition at days 8–14 were significantly higher than days 0–7 (p<0.001). The median %inhibition values by severity of COVID-19 symptoms were 79.9% (interquartile range (IQR) 49.7–91.8%); 89.0% (IQR 71.2–92.4%); and 86.6% (IQR 69.5–92.8%), for mild, moderate and severe/critical symptoms respectively. The median level of sVNT %inhibition of severe was significantly higher than the mild group (p = 0.05). The sVNT is a practical and robust serological test for SARS-CoV-2 infection and does not require specialized biosafety containment. It can be used clinically to aid diagnosis in both early and late infection especially in cases when the real-time RT-PCR results in weakly negative or weakly positive, and to determine the protective immune response from SARS-CoV-2 infection in patients.
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影响因子:
9.4
作者:
Addetia A;Crawford KHD;Dingens A;Zhu H;Roychoudhury P;Huang ML;Jerome KR;Bloom JD;Greninger AL
通讯作者:
Greninger AL
影响因子:
168.9
作者:
Huang, Chaolin;Wang, Yeming;Cao, Bin
通讯作者:
Cao, Bin
影响因子:
15.9
作者:
Wang, Yanqun;Zhang, Lu;Zhao, Jincun
通讯作者:
Zhao, Jincun
DOI:
10.1016/s0140-6736(20)31605-6
发表时间:
2020-08-15
期刊:
Lancet (London, England)
影响因子:
--
作者:
Zhu FC;Guan XH;Li YH;Huang JY;Jiang T;Hou LH;Li JX;Yang BF;Wang L;Wang WJ;Wu SP;Wang Z;Wu XH;Xu JJ;Zhang Z;Jia SY;Wang BS;Hu Y;Liu JJ;Zhang J;Qian XA;Li Q;Pan HX;Jiang HD;Deng P;Gou JB;Wang XW;Wang XH;Chen W
通讯作者:
Chen W
DOI:
10.1001/jama.2020.6775
发表时间:
2020-01-01
期刊:
JAMA, Journal of the American Medical Association
影响因子:
--
作者:
Richardson, Safiya;Hirsch, Jamie S.;,
通讯作者:
,