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Seroprevalence of anti-SARS-CoV-2 antibodies in Japanese COVID-19 patients
To determine the seroprevalence of anti-SARS-CoV-2 IgG and IgM antibodies in symptomatic Japanese COVID-19 patients. Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syn...
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Published in: | PloS one 2021-04, Vol.16 (4), p.e0249449-e0249449 |
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creator | Hiki, Makoto Tabe, Yoko Ai, Tomohiko Matsue, Yuya Harada, Norihiro Sugimoto, Kiichi Matsushita, Yasushi Matsushita, Masakazu Wakita, Mitsuru Misawa, Shigeki Idei, Mayumi Miida, Takashi Tamura, Naoto Takahashi, Kazuhisa Naito, Toshio |
description | To determine the seroprevalence of anti-SARS-CoV-2 IgG and IgM antibodies in symptomatic Japanese COVID-19 patients.
Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were determined by a chemiluminescent microparticle immunoassay (CMIA) using Alinity i SARS-CoV-2 IgG and by an immunochromatographic (IC) IgM/IgG antibody assay using the Anti-SARS-CoV-2 Rapid Test.
IgG was detected by the CMIA in 40%, 88%, and 100% of samples collected within 1 week, 1-2 weeks, and 2 weeks after symptom onset in severe and critical cases, and 0%, 38%, and 100% in mild/moderate cases, respectively. In severe and critical cases, the positive IgG detection rate with the IC assay was 60% within one week and 63% between one and two weeks. In mild/moderate cases, the positive IgG rate was 17% within one week and 63% between one and two weeks; IgM was positive in 80% and 75% of severe and critical cases, and 42% and 88% of mild/moderate cases, respectively. On the CMIA, no anti-SARS-CoV-2 IgG antibodies were detected in COVID-19 outpatients with mild symptoms within 10 days from onset, whereas 50% of samples from severe inpatients were IgG-positive in the same period. The IC assay detected higher IgM positivity earlier from symptom onset in severe and critical cases than in mild/moderate cases.
A serologic anti-SARS-CoV-2 antibody analysis can complement PCR for diagnosing COVID-19 14 days after symptom onset. |
doi_str_mv | 10.1371/journal.pone.0249449 |
format | article |
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Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were determined by a chemiluminescent microparticle immunoassay (CMIA) using Alinity i SARS-CoV-2 IgG and by an immunochromatographic (IC) IgM/IgG antibody assay using the Anti-SARS-CoV-2 Rapid Test.
IgG was detected by the CMIA in 40%, 88%, and 100% of samples collected within 1 week, 1-2 weeks, and 2 weeks after symptom onset in severe and critical cases, and 0%, 38%, and 100% in mild/moderate cases, respectively. In severe and critical cases, the positive IgG detection rate with the IC assay was 60% within one week and 63% between one and two weeks. In mild/moderate cases, the positive IgG rate was 17% within one week and 63% between one and two weeks; IgM was positive in 80% and 75% of severe and critical cases, and 42% and 88% of mild/moderate cases, respectively. On the CMIA, no anti-SARS-CoV-2 IgG antibodies were detected in COVID-19 outpatients with mild symptoms within 10 days from onset, whereas 50% of samples from severe inpatients were IgG-positive in the same period. The IC assay detected higher IgM positivity earlier from symptom onset in severe and critical cases than in mild/moderate cases.
A serologic anti-SARS-CoV-2 antibody analysis can complement PCR for diagnosing COVID-19 14 days after symptom onset.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0249449</identifier><identifier>PMID: 33822809</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibodies ; Antibodies, Viral - blood ; Biology ; Biology and life sciences ; Chemiluminescence ; Coronaviruses ; COVID-19 ; COVID-19 - blood ; COVID-19 - diagnosis ; COVID-19 - epidemiology ; COVID-19 Serological Testing ; Diagnosis ; Editing ; Emergency medical care ; Emergency medical services ; Epidemics ; Female ; Genetic aspects ; Hospitals ; Humans ; IgG antibody ; Immunoassay ; Immunoglobulin G ; Immunoglobulin G - blood ; Immunoglobulin M ; Immunoglobulin M - blood ; Infections ; Internal medicine ; Japan ; Japan - epidemiology ; Male ; Measurement ; Medical innovations ; Medical laboratories ; Medical technology ; Medicine ; Medicine and health sciences ; Methodology ; Microparticles ; Middle Aged ; Monoclonal antibodies ; Mutation ; Olfaction ; Pandemics ; Patients ; Proteins ; Respiratory distress syndrome ; Rheumatology ; SARS-CoV-2 - metabolism ; Serological tests ; Serology ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Supervision ; Surgery ; Thromboembolism ; University faculty ; Viral diseases ; Viruses</subject><ispartof>PloS one, 2021-04, Vol.16 (4), p.e0249449-e0249449</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Hiki et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Hiki et al 2021 Hiki et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-7eb901f8c274c2cdf1140f68d4f3d64a91dcd867ee6dc72271ad9bff126f15453</citedby><cites>FETCH-LOGICAL-c691t-7eb901f8c274c2cdf1140f68d4f3d64a91dcd867ee6dc72271ad9bff126f15453</cites><orcidid>0000-0002-9162-8973 ; 0000-0002-0962-5731 ; 0000-0003-1646-9930</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2509239219?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2509239219?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33822809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hiki, Makoto</creatorcontrib><creatorcontrib>Tabe, Yoko</creatorcontrib><creatorcontrib>Ai, Tomohiko</creatorcontrib><creatorcontrib>Matsue, Yuya</creatorcontrib><creatorcontrib>Harada, Norihiro</creatorcontrib><creatorcontrib>Sugimoto, Kiichi</creatorcontrib><creatorcontrib>Matsushita, Yasushi</creatorcontrib><creatorcontrib>Matsushita, Masakazu</creatorcontrib><creatorcontrib>Wakita, Mitsuru</creatorcontrib><creatorcontrib>Misawa, Shigeki</creatorcontrib><creatorcontrib>Idei, Mayumi</creatorcontrib><creatorcontrib>Miida, Takashi</creatorcontrib><creatorcontrib>Tamura, Naoto</creatorcontrib><creatorcontrib>Takahashi, Kazuhisa</creatorcontrib><creatorcontrib>Naito, Toshio</creatorcontrib><title>Seroprevalence of anti-SARS-CoV-2 antibodies in Japanese COVID-19 patients</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>To determine the seroprevalence of anti-SARS-CoV-2 IgG and IgM antibodies in symptomatic Japanese COVID-19 patients.
Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were determined by a chemiluminescent microparticle immunoassay (CMIA) using Alinity i SARS-CoV-2 IgG and by an immunochromatographic (IC) IgM/IgG antibody assay using the Anti-SARS-CoV-2 Rapid Test.
IgG was detected by the CMIA in 40%, 88%, and 100% of samples collected within 1 week, 1-2 weeks, and 2 weeks after symptom onset in severe and critical cases, and 0%, 38%, and 100% in mild/moderate cases, respectively. In severe and critical cases, the positive IgG detection rate with the IC assay was 60% within one week and 63% between one and two weeks. In mild/moderate cases, the positive IgG rate was 17% within one week and 63% between one and two weeks; IgM was positive in 80% and 75% of severe and critical cases, and 42% and 88% of mild/moderate cases, respectively. On the CMIA, no anti-SARS-CoV-2 IgG antibodies were detected in COVID-19 outpatients with mild symptoms within 10 days from onset, whereas 50% of samples from severe inpatients were IgG-positive in the same period. The IC assay detected higher IgM positivity earlier from symptom onset in severe and critical cases than in mild/moderate cases.
A serologic anti-SARS-CoV-2 antibody analysis can complement PCR for diagnosing COVID-19 14 days after symptom onset.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies</subject><subject>Antibodies, Viral - blood</subject><subject>Biology</subject><subject>Biology and life sciences</subject><subject>Chemiluminescence</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - blood</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 - epidemiology</subject><subject>COVID-19 Serological Testing</subject><subject>Diagnosis</subject><subject>Editing</subject><subject>Emergency medical care</subject><subject>Emergency medical services</subject><subject>Epidemics</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>IgG antibody</subject><subject>Immunoassay</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulin M - blood</subject><subject>Infections</subject><subject>Internal medicine</subject><subject>Japan</subject><subject>Japan - epidemiology</subject><subject>Male</subject><subject>Measurement</subject><subject>Medical innovations</subject><subject>Medical laboratories</subject><subject>Medical technology</subject><subject>Medicine</subject><subject>Medicine and health sciences</subject><subject>Methodology</subject><subject>Microparticles</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Olfaction</subject><subject>Pandemics</subject><subject>Patients</subject><subject>Proteins</subject><subject>Respiratory distress syndrome</subject><subject>Rheumatology</subject><subject>SARS-CoV-2 - metabolism</subject><subject>Serological tests</subject><subject>Serology</subject><subject>Severe acute respiratory syndrome</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Supervision</subject><subject>Surgery</subject><subject>Thromboembolism</subject><subject>University faculty</subject><subject>Viral 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Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hiki, Makoto</au><au>Tabe, Yoko</au><au>Ai, Tomohiko</au><au>Matsue, Yuya</au><au>Harada, Norihiro</au><au>Sugimoto, Kiichi</au><au>Matsushita, Yasushi</au><au>Matsushita, Masakazu</au><au>Wakita, Mitsuru</au><au>Misawa, Shigeki</au><au>Idei, Mayumi</au><au>Miida, Takashi</au><au>Tamura, Naoto</au><au>Takahashi, Kazuhisa</au><au>Naito, Toshio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Seroprevalence of anti-SARS-CoV-2 antibodies in Japanese COVID-19 patients</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2021-04-06</date><risdate>2021</risdate><volume>16</volume><issue>4</issue><spage>e0249449</spage><epage>e0249449</epage><pages>e0249449-e0249449</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>To determine the seroprevalence of anti-SARS-CoV-2 IgG and IgM antibodies in symptomatic Japanese COVID-19 patients.
Serum samples (n = 114) from 34 COVID-19 patients with mild to critical clinical manifestations were examined. The presence and titers of IgG antibody for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were determined by a chemiluminescent microparticle immunoassay (CMIA) using Alinity i SARS-CoV-2 IgG and by an immunochromatographic (IC) IgM/IgG antibody assay using the Anti-SARS-CoV-2 Rapid Test.
IgG was detected by the CMIA in 40%, 88%, and 100% of samples collected within 1 week, 1-2 weeks, and 2 weeks after symptom onset in severe and critical cases, and 0%, 38%, and 100% in mild/moderate cases, respectively. In severe and critical cases, the positive IgG detection rate with the IC assay was 60% within one week and 63% between one and two weeks. In mild/moderate cases, the positive IgG rate was 17% within one week and 63% between one and two weeks; IgM was positive in 80% and 75% of severe and critical cases, and 42% and 88% of mild/moderate cases, respectively. On the CMIA, no anti-SARS-CoV-2 IgG antibodies were detected in COVID-19 outpatients with mild symptoms within 10 days from onset, whereas 50% of samples from severe inpatients were IgG-positive in the same period. The IC assay detected higher IgM positivity earlier from symptom onset in severe and critical cases than in mild/moderate cases.
A serologic anti-SARS-CoV-2 antibody analysis can complement PCR for diagnosing COVID-19 14 days after symptom onset.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>33822809</pmid><doi>10.1371/journal.pone.0249449</doi><tpages>e0249449</tpages><orcidid>https://orcid.org/0000-0002-9162-8973</orcidid><orcidid>https://orcid.org/0000-0002-0962-5731</orcidid><orcidid>https://orcid.org/0000-0003-1646-9930</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2021-04, Vol.16 (4), p.e0249449-e0249449 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2509239219 |
source | Publicly Available Content Database; PubMed Central; Coronavirus Research Database |
subjects | Adult Aged Aged, 80 and over Antibodies Antibodies, Viral - blood Biology Biology and life sciences Chemiluminescence Coronaviruses COVID-19 COVID-19 - blood COVID-19 - diagnosis COVID-19 - epidemiology COVID-19 Serological Testing Diagnosis Editing Emergency medical care Emergency medical services Epidemics Female Genetic aspects Hospitals Humans IgG antibody Immunoassay Immunoglobulin G Immunoglobulin G - blood Immunoglobulin M Immunoglobulin M - blood Infections Internal medicine Japan Japan - epidemiology Male Measurement Medical innovations Medical laboratories Medical technology Medicine Medicine and health sciences Methodology Microparticles Middle Aged Monoclonal antibodies Mutation Olfaction Pandemics Patients Proteins Respiratory distress syndrome Rheumatology SARS-CoV-2 - metabolism Serological tests Serology Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Supervision Surgery Thromboembolism University faculty Viral diseases Viruses |
title | Seroprevalence of anti-SARS-CoV-2 antibodies in Japanese COVID-19 patients |
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