The role and diagnostic accuracy of serology for COVID-19

被引:9
|
作者
Kundu, Debasree [1 ]
Gautam, Priyanka [1 ]
Dayanand, Divya [1 ]
Gunasekaran, Karthik [2 ]
Manesh, Abi [1 ]
Sebastian, Merylin [1 ]
Abhilash, Kundavaram P. P. [3 ]
Zachariah, Anand [2 ]
George, Tina [2 ]
Sathyendra, Sowmya [2 ]
Hansdak, Samuel G. [2 ]
Abraham, O. C. [2 ]
Iyadurai, Ramya [2 ]
Thangakunam, Balamugesh [4 ]
Gupta, Richa [5 ]
Karthik, Rajiv [1 ]
Moorthy, Mahesh [6 ]
Varghese, George M. [1 ]
机构
[1] Christian Med Coll & Hosp, Dept Infect Dis, Vellore 632004, Tamil Nadu, India
[2] Christian Med Coll & Hosp, Dept Med, Vellore, Tamil Nadu, India
[3] Christian Med Coll & Hosp, Dept Emergency Med, Vellore, Tamil Nadu, India
[4] Christian Med Coll & Hosp, Dept Pulm Med, Vellore, Tamil Nadu, India
[5] Christian Med Coll & Hosp, Dept Resp Med, Vellore, Tamil Nadu, India
[6] Christian Med Coll & Hosp, Dept Clin Virol, Vellore, Tamil Nadu, India
基金
英国惠康基金;
关键词
COVID-19; SARS-CoV-2; Antibody test; IgM; IgG; Serology; CORONAVIRUS DISEASE 2019;
D O I
10.1186/s12879-022-07361-y
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The role and performance of various serological tests for the diagnosis of COVID-19 are unclear. This study aimed to evaluate the performance of seven commercially available serological assays for SARS-CoV-2 antibodies by testing COVID-19 cases and controls. Methods Adult patients with fever for > 5 days, admitted to a tertiary-care teaching hospital in South India, were enrolled prospectively between June and December 2020. SARS-CoV-2 RT-PCR confirmed patients were classified as cases, and patients with febrile illness with laboratory-confirmed alternative diagnosis and healthy participants were controls. All participants were tested with SCoV-2 Detect (TM) IgM ELISA kit and SCoV-2 Detect (TM) IgG ELISA kit (InBios International, Seattle, USA) (Inbios), SARS-CoV-2 Total and SARS-CoV-2 IgG (Siemens Healthcare Diagnostics Inc., Tarrytown, USA) (Siemens), Roche Elecsys (R) Anti-SARS-CoV-2 (Roche Diagnostics, Rotkreuz, Switzerland) (Roche), Abbott SARS-CoV-2 IgG (Abbott Diagnostics, IL, USA) (Abbott), and Liaison (R) SARS-CoV-2 S1/S2 IgG (DiaSorinS.p.A., Saluggia, Italy) (Liaison). The sensitivities, specificities, positive predictive values (PPV), negative predictive values (NPV), and accuracies were compared. Results There were 303 participants: 153 cases and 150 controls. ELISA detecting anti-S protein antibody was more sensitive (88.9% for IgG and 86.3% for IgM) than the CLIAs (82.4% for total antibodies and 76.5-85.6% for IgG). Among CLIAs, Roche IgG was most sensitive (85.6%) followed by Abbott (83%) and Liaison (83%). Abbot had the best PPV (88.8%) and was more specific (89.3%) than Liaison (82%) and Roche (82%). Siemens IgG was less sensitive (76.5%) than Siemens Total (82.4%). The specificity of all the serological assays was modest (75-90%). Antibody test positivity increased with the duration of illness reaching 90% after 10 days of illness. When cases were compared against pre-pandemic controls, the IgG gave excellent specificity (98-100%). For seroprevalence studies, InBios IgG had the best accuracy (90.8%) with 88.9% sensitivity and 97.6% specificity. Conclusion The serological assays are important adjuncts for the diagnosis of COVID-19 in patients with persistent symptoms, especially in the second week of illness. The value of serological diagnostic tests is limited in the first week of illness and they provide additional value in seroprevalence studies. The diagnostic accuracy of the ELISA and CLIA platforms were comparable.
引用
收藏
页数:8
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