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About:
The production of antibodies for SARS-CoV-2 and its clinical implication
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
The production of antibodies for SARS-CoV-2 and its clinical implication
Creator
Li, Yan
Duan, Jun
Wang, Xue
Guo, Shuliang
Hu, Qianfang
Hu, Wenhui
Zhu, Linxiao
Ao, Zhi
Cui, Xiaoping
Jiang, Jinyue
Liu, Xinzhu
Wang, ,
Wu, Guicheng
Source
MedRxiv
abstract
Background: Severe acute respiratory syndrome coronavirus 2(SARS-CoV-2), a novel betacoronavirus, has caused an outburst of pneumonia cases in Wuhan, China. We report the production of specific IgM and IgG antibodies after the infection of SARS-CoV-2 and its implication for the diagnosis, pathology and the course of the disease as well as the recurrence of positive nucleic acid tests after discharge. Methods: Test results for SARS-CoV-2 IgM and IgG antibodies of 221 confirmed COVID-19 patients were retrospectively examined, and their clinical data were collected and analyzed based on various subgroups. SARS-CoV-2 IgM and IgG antibodies were determined with the chemiluminescence method. Findings: The concentration (S/CO) of SARS-CoV-2 IgM and IgG antibodies peaked on day 19-21 after symptom onset, with a median of 17.38 (IQR 4.39-36.4) for IgM and 5.59 (IQR 0.73-13.65) for IgG. Detection rates reached highest on day 16-18 and day 19-21 for IgM and IgG, which were 73.6% and 98.6%, respectively, with significantly higher concentration of IgG in critically ill patients than in those with mild to moderate disease (P=0.027). The concentration of the antibodies on day 16-21 is not correlated with the course or outcome of the disease (Spearman r < 0.20, P > 0.05). Nasopharyngeal swabs revealed positive SARS-CoV-2 RNA in up to 52.7% of recovered patients after discharge, whose IgG proved to be significantly lower than that of those with negative RNA results (P = 0.009). IgG and IgM were tested twice within 14 days after discharge with a 7-day interval, and the second testing of these antibodies displayed a decrease in concentration of 21.2% (IQR, 11.2%34.48%) for IgG and 23.05% (IQR, -27.96%46.13%) for IgM, without statistical significance between the patients with re-detectable positive RNA results and those with negative RNA results after discharge. However, those with positive results experienced a count decrease in lymphocyte subsets. Interpretation: The concentration of SARS-CoV-2 IgM and IgG antibodies peaked on day 19-21 after symptom onset, and antibody testing on day 16-21 is associated with increased detection rates, but the antibody concentration does not affect the course and outcome of the infection. Recovering patients with re-detectable positive SARS-CoV-2 RNA displayed lower concentration of IgG, but the downward trend of IgG during recovery indicated its limited duration of protection, and the protective effect of IgG remains to be investigated.
has issue date
2020-04-24
(
xsd:dateTime
)
bibo:doi
10.1101/2020.04.20.20065953
has license
medrxiv
sha1sum (hex)
68c9c407f9ff722f6b28052910f915cad6eeca44
schema:url
https://doi.org/10.1101/2020.04.20.20065953
resource representing a document's title
The production of antibodies for SARS-CoV-2 and its clinical implication
resource representing a document's body
covid:68c9c407f9ff722f6b28052910f915cad6eeca44#body_text
is
schema:about
of
named entity 'Education'
named entity 'EDUCATION'
named entity 'antibodies'
named entity 'implications'
named entity 'FITC'
named entity 'IgG'
named entity 'radiology'
named entity 'symptom'
named entity 'IgG antibodies'
named entity 'IgM antibodies'
named entity 'antibody'
named entity 'fever'
named entity 'IgG'
named entity 'SARS-CoV-2'
named entity 'medRxiv'
named entity 'SARS-CoV-2'
named entity 'IgG'
named entity 'nasopharyngeal swabs'
named entity 'Chongqing'
named entity 'antibodies'
named entity 'IgM antibodies'
named entity 'RNA'
named entity 'standard deviation'
named entity 'IgG'
named entity 'chemiluminescence'
named entity 'nucleic acid'
named entity 'CD8'
named entity 'medRxiv'
named entity 'coronavirus'
named entity 'IgM'
named entity 'nucleic acid testing'
named entity 'COVID'
named entity 'SARS-CoV-2'
named entity 'interquartile range'
named entity 'RT-PCR'
named entity 'statistical analysis'
named entity 'data acquisition'
named entity 'statistically significant'
named entity 'early diagnosis'
named entity 'fluorescein isothiocyanate'
named entity 'antibody tests'
named entity 'prognosis'
named entity 'early diagnosis'
named entity 'nucleic acid'
named entity 'epidemic'
named entity 'medRxiv'
named entity 'immunoassay'
named entity 'immune complex'
named entity 'pathogen'
named entity 'IgG'
named entity 'IgG'
named entity 'nucleic acid testing'
named entity 'epidemic'
named entity 'antibody'
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named entity 'follow-up'
named entity 'SARS-CoV-2'
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named entity 'informed consent'
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named entity 'IgM'
named entity 'China'
named entity 'peer review'
named entity 'polynomial regression'
named entity 'COVID'
named entity 'informed consent'
named entity 'antibodies'
named entity 'study protocol'
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