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Early peripheral blood MCEMP1 and HLA-DRA expression predicts COVID-19 prognosis.
Chan, Kuan Rong; Koh, Clara W T; Ng, Dorothy H L; Qin, Shijie; Ooi, Justin S G; Ong, Eugenia Z; Zhang, Summer L X; Sam, Huizhen; Kalimuddin, Shirin; Low, Jenny G H; Ooi, Eng Eong.
Afiliación
  • Chan KR; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore. Electronic address: kuanrong.chan@duke-nus.edu.sg.
  • Koh CWT; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • Ng DHL; Department of Infectious Diseases, Singapore General Hospital, Singapore.
  • Qin S; Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences (CAS), Beijing, 100101, China.
  • Ooi JSG; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • Ong EZ; Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences (CAS), Beijing, 100101, China.
  • Zhang SLX; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • Sam H; Department of Infectious Diseases, Singapore General Hospital, Singapore.
  • Kalimuddin S; Department of Infectious Diseases, Singapore General Hospital, Singapore.
  • Low JGH; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore; Department of Infectious Diseases, Singapore General Hospital, Singapore; Viral Research and Experimental Medicine Centre, SingHealth Duke-NUS Academic Medical Centre, Singapore.
  • Ooi EE; Department of Infectious Diseases, Singapore General Hospital, Singapore; Viral Research and Experimental Medicine Centre, SingHealth Duke-NUS Academic Medical Centre, Singapore; Saw Swee Hock School of Public Health, National University of Singapore, Singapore.
EBioMedicine ; 89: 104472, 2023 Mar.
Article en En | MEDLINE | ID: mdl-36801619
BACKGROUND: Mass vaccination has dramatically reduced the incidence of severe COVID-19, with most cases now presenting as self-limiting upper respiratory tract infections. However, those with co-morbidities, the elderly and immunocompromised, as well as the unvaccinated, remain disproportionately vulnerable to severe COVID-19 and its sequelae. Furthermore, as the effectiveness of vaccination wanes with time, immune escape SARS-CoV-2 variants could emerge to cause severe COVID-19. Reliable prognostic biomarkers for severe disease could be used as early indicator of re-emergence of severe COVID-19 as well as for triaging of patients for antiviral therapy. METHODS: We performed a systematic review and re-analysis of 7 publicly available datasets, analysing a total of 140 severe and 181 mild COVID-19 patients, to determine the most consistent differentially regulated genes in peripheral blood of severe COVID-19 patients. In addition, we included an independent cohort where blood transcriptomics of COVID-19 patients were prospectively and longitudinally monitored previously, to track the time in which these gene expression changes occur before nadir of respiratory function. Single cell RNA-sequencing of peripheral blood mononuclear cells from publicly available datasets was then used to determine the immune cell subsets involved. FINDINGS: The most consistent differentially regulated genes in peripheral blood of severe COVID-19 patients were MCEMP1, HLA-DRA and ETS1 across the 7 transcriptomics datasets. Moreover, we found significantly heightened MCEMP1 and reduced HLA-DRA expression as early as four days before the nadir of respiratory function, and the differential expression of MCEMP1 and HLA-DRA occurred predominantly in CD14+ cells. The online platform which we developed is publicly available at https://kuanrongchan-covid19-severity-app-t7l38g.streamlitapp.com/, for users to query gene expression differences between severe and mild COVID-19 patients in these datasets. INTERPRETATION: Elevated MCEMP1 and reduced HLA-DRA gene expression in CD14+ cells during the early phase of disease are prognostic of severe COVID-19. FUNDING: K.R.C is funded by the National Medical Research Council (NMRC) of Singapore under the Open Fund Individual Research Grant (MOH-000610). E.E.O. is funded by the NMRC Senior Clinician-Scientist Award (MOH-000135-00). J.G.H.L. is funded by the NMRC under the Clinician-Scientist Award (NMRC/CSAINV/013/2016-01). S.K. is funded by the NMRC under the Transition Award. This study was sponsored in part by a generous gift from The Hour Glass.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Aged / Humans Idioma: En Revista: EBioMedicine Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Aged / Humans Idioma: En Revista: EBioMedicine Año: 2023 Tipo del documento: Article