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10.1016/j.jviromet.2020.113996

http://scihub22266oqcxt.onion/10.1016/j.jviromet.2020.113996
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suck abstract from ncbi


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pmid33126149      J+Virol+Methods 2021 ; 287 (ä): 113996
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  • Anti-SARS-CoV-2 IgG antibody response among Indian COVID-19 patients using beta-propiolactone-inactivated, whole virus-based indirect ELISA #MMPMID33126149
  • Kulkarni R; Patil HP; Palkar S; Lalwani S; Mishra AC; Arankalle V
  • J Virol Methods 2021[Jan]; 287 (ä): 113996 PMID33126149show ga
  • BACKGROUND: Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome - coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations. METHODS: An indirect IgG ELISA was developed indigenously using beta-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017-2019), 185 serum/plasma samples of confirmed COVID-19 patients (n?=?137) and 57 samples of viral RNA positive asymptomatic contacts (n?=?51). The IgG response was studied in relation to duration and severity of illness. RESULTS: The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P?=?0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P?
  • |Antibodies, Viral/blood[MESH]
  • |COVID-19 Serological Testing/*methods[MESH]
  • |COVID-19/blood/*diagnosis/pathology[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*blood[MESH]
  • |Propiolactone/*pharmacology[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Sensitivity and Specificity[MESH]
  • |Seroepidemiologic Studies[MESH]


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