Mengyu Chen, Rundong Qin, Mei Jiang, Zhaowei Yang, Weiping Wen, Jing Li
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2021;104():415-422
PMID: 33450372
The rapidly spreading nature of COVID-19 has put an emphasis on the importance of fast diagnosis. Gold standard diagnosis is through reverse transcription polymerase chain reaction (RT-PCR) tests, which aims to detect the presence of COVID-19. However, challenges with collection techniques and when in the disease lifecycle these tests are taken, can affect their reliability, highlighting a need for alternative methods of testing. Other testing methods exist, which involve testing the body’s own immune response to the presence of COVID-19, however these may also have their limitations. This systematic review and meta-analysis aimed to determine the effectiveness of testing the body’s own immune reaction for the presence of COVID-19. The results showed that testing the body’s immune reaction was effective, however if the person being tested is at an early stage in the disease, then it may be misdiagnosed. This study could be used by healthcare professionals to understand that the use of any type of COVID-19 testing may have its limitations, and although a person may test negative, there is still a possibility that they have the infection if symptoms exist
BACKGROUND
The coronavirus disease 2019 (COVID-19) pandemic has had a devastating impact worldwide, and timely detection and quarantine of infected patients are critical to prevent spread of disease. Serological antibody testing is an important diagnostic method used increasingly in clinics, although its clinical application is still under investigation.
METHODS
A meta-analysis was conducted to compare the diagnostic performance of severe acute respiratory syndrome coronavirus-2 antibody tests in patients with COVID-19. The test results analysed included: (1) IgM-positive but IgG-negative (IgMIgG); (2) IgG-positive but IgM-negative (IgGIgM); (3) both IgM-positive and IgG-positive (IgMIgG); (4) IgM-positive without IgG information (IgMIgG); (5) IgG-positive without IgM information (IgGIgM); (6) either IgM-positive or IgG-positive (IgM or IgG); and (7) IgA-positive (IgA).
RESULTS
Sixty-eight studies were included. Pooled sensitivities for IgMIgG, IgGIgM, IgMIgG, IgMIgG, IgGIgM, and IgM or IgG were 6%, 7%, 53%, 68%, 73% and 79% respectively. Pooled specificities ranged from 98% to 100%. IgA had a pooled sensitivity of 78% but a relatively low specificity of 88%. Tests conducted 2 weeks after symptom onset showed better diagnostic accuracy than tests conducted earlier. Chemiluminescence immunoassay and detection of S protein as the antigen could offer more accurate diagnostic results.
DISCUSSION
These findings support the supplemental role of serological antibody tests in the diagnosis of COVID-19. However, their capacity to diagnose COVID-19 early in the disease course could be limited.
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
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