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10.1186/s12879-021-05878-2

http://scihub22266oqcxt.onion/10.1186/s12879-021-05878-2
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33602152!7889711!33602152
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suck abstract from ncbi


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pmid33602152      BMC+Infect+Dis 2021 ; 21 (1): 187
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  • Stringent thresholds in SARS-CoV-2 IgG assays lead to under-detection of mild infections #MMPMID33602152
  • Eyre DW; Lumley SF; O'Donnell D; Stoesser NE; Matthews PC; Howarth A; Hatch SB; Marsden BD; Cox S; James T; Cornall RJ; Stuart DI; Screaton G; Ebner D; Crook DW; Conlon CP; Jeffery K; Walker TM; Peto TEA
  • BMC Infect Dis 2021[Feb]; 21 (1): 187 PMID33602152show ga
  • BACKGROUND: Thresholds for SARS-CoV-2 antibody assays have typically been determined using samples from symptomatic, often hospitalised, patients. In this setting the sensitivity and specificity of the best performing assays can both exceed 98%. However, antibody assay performance following mild infection is less clear. METHODS: We assessed quantitative IgG responses in a cohort of healthcare workers in Oxford, UK, with a high pre-test probability of Covid-19, in particular the 991/11,475(8.6%) who reported loss of smell/taste. We use anosmia/ageusia and other risk factors as probes for Covid-19 infection potentially undiagnosed by immunoassays by investigating their relationship with antibody readings either side of assay thresholds. RESULTS: The proportion of healthcare workers reporting anosmia/ageusia increased at antibody readings below diagnostic thresholds using an in-house ELISA (n = 9324) and the Abbott Architect chemiluminescent microparticle immunoassay (CMIA; n = 11,324): 426/906 (47%) reported anosmia/ageusia with a positive ELISA, 59/449 (13.1%) with high-negative and 326/7969 (4.1%) with low-negative readings. Similarly, by CMIA, 518/1093 (47.4%) with a positive result reported anosmia/ageusia, 106/686 (15.5%) with a high-negative and 358/9563 (3.7%) with a low-negative result. Adjusting for the proportion of staff reporting anosmia/ageusia suggests the sensitivity of both assays in mild infection is lower than previously reported: Oxford ELISA 89.8% (95%CI 86.6-92.8%) and Abbott CMIA 79.3% (75.9-82.7%). CONCLUSION: Following mild SARS-CoV-2 infection 10-30% of individuals may have negative immunoassay results. While lowered diagnostic thresholds may result in unacceptable specificity, our findings have implications for epidemiological analyses and result interpretation in individuals with a high pre-test probability. Samples from mild PCR-confirmed infections should be included in SARS-CoV-2 immunoassay evaluations.
  • |Adult[MESH]
  • |Ageusia/virology[MESH]
  • |Anosmia/virology[MESH]
  • |Antibodies, Viral/*analysis[MESH]
  • |Asymptomatic Infections[MESH]
  • |COVID-19 Serological Testing/*standards[MESH]
  • |COVID-19/*diagnosis[MESH]
  • |Enzyme-Linked Immunosorbent Assay/standards[MESH]
  • |Female[MESH]
  • |Health Personnel[MESH]
  • |Humans[MESH]
  • |Immunoassay/standards[MESH]
  • |Immunoglobulin G/*analysis[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Sensitivity and Specificity[MESH]
  • |Undiagnosed Diseases[MESH]


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