Статья

Laboratory-based resources for COVID-19 diagnostics: Traditional tools and novel technologies. a perspective of personalized medicine

B. Andryukov, N. Besednova, T. Kuznetsova, L. Fedyanina,
2021

The coronavirus infection 2019 (COVID-19) pandemic, caused by the highly contagious SARS-CoV-2 virus, has provoked a global healthcare and economic crisis. The control over the spread of the disease requires an efficient and scalable laboratory-based strategy for testing the population based on multiple platforms to provide rapid and accurate diagnosis. With the onset of the pan-demic, the reverse transcription polymerase chain reaction (RT-PCR) method has become a standard diagnostic tool, which has received wide clinical use. In large-scale and repeated examinations, these tests can identify infected patients with COVID-19, with their accuracy, however, dependent on many factors, while the entire process takes up to 6–8 h. Here we also describe a number of serological systems for detecting antibodies against SARS-CoV-2. These are used to assess the level of population immunity in various categories of people, as well as for retrospective diagnosis of asymptomatic and mild COVID-19 in patients. However, the widespread use of traditional diagnostic tools in the context of the rapid spread of COVID-19 is hampered by a number of limitations. Therefore, the sharp increase in the number of patients with COVID-19 necessitates creation of new rapid, inexpensive, sensitive, and specific tests. In this regard, we focus on new laboratory technologies such as loop mediated isothermal amplification (LAMP) and lateral flow immunoassay (LFIA), which have proven to work well in the COVID-19 diagnostics and can become a worthy alternative to traditional laboratory-based diagnostics resources. To cope with the COVID-19 pandemic, the healthcare system requires a combination of various types of laboratory diagnostic testing techniques, whodse sensitivity and specificity increases with the progress in the SARS-CoV-2 research. The testing strategy should be designed in such a way to provide, depending on the timing of examination and the severity of the infection in patients, large-scale and repeated examinations based on the principle: screening–monitoring–control. The search and development of new methods for rapid diagnostics of COVID-19 in laboratory, based on new analytical platforms, is still a highly important and urgent healthcare issue. In the final part of the review, special emphasis is made on the relevance of the concept of personalized medicine to combat the COVID-19 pandemic in the light of the recent studies carried out to identify the causes of variation in individual susceptibility to SARS-CoV-2 and increase the efficiency and cost-effectiveness of treatment. © 2021 by the authors. Li-censee MDPI, Basel, Switzerland.

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Версии

  • 1. Version of Record от 2021-04-27

Метаданные

Об авторах
  • B. Andryukov
    G.P. Somov Institute of Epidemiology and Microbiology, Russian Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, Vladivostok, 690087, Russian Federation
  • N. Besednova
    School of Biomedicine, Far Eastern Federal University (FEFU), Vladivostok, 690091, Russian Federation
  • T. Kuznetsova
  • L. Fedyanina
Название журнала
  • Journal of Personalized Medicine
Том
  • 11
Выпуск
  • 1
Страницы
  • 1-25
Ключевые слова
  • biological marker; immunoglobulin G; immunoglobulin M; asymptomatic disease; coronavirus disease 2019; cost effectiveness analysis; diagnostic test accuracy study; enzyme linked immunosorbent assay; health care system; human; immunoassay; lateral flow immunoassay; loop mediated isothermal amplification; nasopharyngeal swab; oropharyngeal swab; pandemic; personalized medicine; reverse transcription polymerase chain reaction; Review; SARS coronavirus; sensitivity and specificity; sputum smear
Издатель
  • MDPI AG
Тип документа
  • Review
Тип лицензии Creative Commons
  • CC
Правовой статус документа
  • Свободная лицензия
Источник
  • scopus