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Establishment of the large-scale longitudinal multi-omics dataset in COVID-19 patients: data profile and biospecimen

  • Jo, Hye-Yeong (Division of Healthcare and Artificial Intelligence, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Kim, Sang Cheol (Division of Healthcare and Artificial Intelligence, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Ahn, Do-hwan (Division of Healthcare and Artificial Intelligence, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Lee, Siyoung (Geninus Inc) ;
  • Chang, Se-Hyun (Division of Healthcare and Artificial Intelligence, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Jung, So-Young (Division of Biobank, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Kim, Young-Jin (Division of Genome Science, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Kim, Eugene (Division of Biobank, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Kim, Jung-Eun (Division of Bio Bigdata, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Kim, Yeon-Sook (Division of Infectious Disease, Department of Internal Medicine, Chungnam National University School of Medicine) ;
  • Park, Woong-Yang (Geninus Inc) ;
  • Cho, Nam-Hyuk (Department of Microbiology and Immunology, College of Medicine, Seoul National University) ;
  • Park, Donghyun (Geninus Inc) ;
  • Lee, Ju-Hee (Division of Healthcare and Artificial Intelligence, Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency) ;
  • Park, Hyun-Young (Department of Precision Medicine, Korea National Institute of Health, Korea Disease Control and Prevention Agency)
  • Received : 2022.05.09
  • Accepted : 2022.07.29
  • Published : 2022.09.30

Abstract

Understanding and monitoring virus-mediated infections has gained importance since the global outbreak of the coronavirus disease 2019 (COVID-19) pandemic. Studies of high-throughput omics-based immune profiling of COVID-19 patients can help manage the current pandemic and future virus-mediated pandemics. Although COVID-19 is being studied since past 2 years, detailed mechanisms of the initial induction of dynamic immune responses or the molecular mechanisms that characterize disease progression remains unclear. This study involved comprehensively collected biospecimens and longitudinal multi-omics data of 300 COVID-19 patients and 120 healthy controls, including whole genome sequencing (WGS), single-cell RNA sequencing combined with T cell receptor (TCR) and B cell receptor (BCR) sequencing (scRNA(+scTCR/BCR)-seq), bulk BCR and TCR sequencing (bulk TCR/BCR-seq), and cytokine profiling. Clinical data were also collected from hospitalized COVID-19 patients, and HLA typing, laboratory characteristics, and COVID-19 viral genome sequencing were performed during the initial diagnosis. The entire set of biospecimens and multi-omics data generated in this project can be accessed by researchers from the National Biobank of Korea with prior approval. This distribution of large-scale multi-omics data of COVID-19 patients can facilitate the understanding of biological crosstalk involved in COVID-19 infection and contribute to the development of potential methodologies for its diagnosis and treatment.

Keywords

Acknowledgement

We acknowledge all the healthcare workers involved in this study from the Chungnam National University Hospital, Seoul Medical Center, and Samsung Medical Center for their efforts in collecting samples and creating medical records. We also thank all the managers and staff at the hospitals and biobank for sample handling and preprocessing, as well as for the production of high-quality data. This work was supported by the Korea National Institute of Health Infrastructural Research Program 4800-4861-312-210-13 and operation of data center for national biomedical data resources (2021-NI-017-00).

References

  1. Coronaviridae Study Group of the International Committee on Taxonomy of V (2020) The species severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2. Nat Microbiol 5, 536-544 https://doi.org/10.1038/s41564-020-0695-z
  2. World Health Organization (January 2020) Surveillance case definitions for human infection with novel coronavirus (nCoV): interim guidance v1. (https://apps.who.int/iris/handle/10665/330376.
  3. Ministry of Health and Welfare (10 March 2022); https://ncov.mohw.go.kr/.
  4. Stephenson E, Reynolds G, Botting RA et al (2021) Single-cell multi-omics analysis of the immune response in COVID-19. Nat Med 27, 904-916 https://doi.org/10.1038/s41591-021-01329-2
  5. Bernardes JP, Mishra N, Tran F et al (2020) Longitudinal multi-omics analyses identify responses of megakaryocytes, erythroid cells, and plasmablasts as hallmarks of severe COVID-19. Immunity 53, 1296-1314 e1299
  6. Wang S, Yao X, Ma S et al (2021) A single-cell transcriptomic landscape of the lungs of patients with COVID-19. Nat Cell Biol 23, 1314-1328 https://doi.org/10.1038/s41556-021-00796-6
  7. Delorey TM, Ziegler CGK, Heimberg G et al (2021) COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets. Nature 595, 107-113 https://doi.org/10.1038/s41586-021-03570-8
  8. Overmyer KA, Shishkova E, Miller IJ et al (2021) Large-scale multi-omic analysis of COVID-19 severity. Cell Syst 12, 23-40 e27
  9. Wu P, Chen D, Ding W et al (2021) The trans-omics landscape of COVID-19. Nat Commun 12, 4543
  10. Huang SF, Huang YC, Chang FY et al (2020) Rapid establishment of a COVID-19 biobank in NHRI by National Biobank Consortium of Taiwan. Biomed J 43, 314-317 https://doi.org/10.1016/j.bj.2020.05.018
  11. Holub P, Kozera L, Florindi F et al (2020) BBMRI-ERIC's contributions to research and knowledge exchange on COVID-19. Eur J Hum Genet 28, 728-731 https://doi.org/10.1038/s41431-020-0634-8
  12. Feldstein LR, Rose EB, Horwitz SM et al (2020) Multisystem inflammatory syndrome in U.S. children and adolescents. N Engl J Med 383, 334-346 https://doi.org/10.1056/NEJMoa2021680
  13. Iyer M, Jayaramayya K, Subramaniam MD et al (2020) COVID-19: an update on diagnostic and therapeutic approaches. BMB Rep 53, 191-205 https://doi.org/10.5483/BMBRep.2020.53.4.080
  14. National Institute of Health (NIH) (March 2022) Clinical spectrum of SARS-CoV-2 infection : https://www.covid19treatmentguidelines.nih.gov/overview/clinical-spectrum/
  15. An H, Zhang J, Li T et al (2022) Inflammation/coagulo pathy/immunology responsive index predicts poor COVID-19 prognosis. Front Cell Infect Microbiol 12, 807332
  16. He C, Liu C, Yang J et al (2022) Prognostic significance of day-by-day in-hospital blood pressure variability in COVID-19 patients with hypertension. J Clin Hypertens (Greenwich) 24, 224-233 https://doi.org/10.1111/jch.14437
  17. Kappert K, Jahic A and Tauber R (2020) Assessment of serum ferritin as a biomarker in COVID-19: bystander or participant? Insights by comparison with other infectious and non-infectious diseases. Biomarkers 25, 616-625 https://doi.org/10.1080/1354750X.2020.1797880
  18. Carubbi F, Salvati L, Alunno A et al (2021) Ferritin is associated with the severity of lung involvement but not with worse prognosis in patients with COVID-19: data from two Italian COVID-19 units. Sci Rep 11, 4863
  19. Alunno A, Carubbi F and Rodriguez-Carrio J (2020) Storm, typhoon, cyclone or hurricane in patients with COVID-19? Beware of the same storm that has a different origin. RMD Open 6, e001295
  20. Chakurkar V, Rajapurkar M, Lele S et al (2021) Increased serum catalytic iron may mediate tissue injury and death in patients with COVID-19. Sci Rep 11, 19618
  21. Biamonte F, Botta C, Mazzitelli M et al (2021) Combined lymphocyte/monocyte count, D-dimer and iron status predict COVID-19 course and outcome in a long-term care facility. J Transl Med 19, 79
  22. Han H, Ma Q, Li C et al (2020) Profiling serum cytokines in COVID-19 patients reveals IL-6 and IL-10 are disease severity predictors. Emerg Microbes Infect 9, 1123-1130 https://doi.org/10.1080/22221751.2020.1770129
  23. Ling L, Chen Z, Lui G et al (2021) Longitudinal cytokine profile in patients with mild to critical COVID-19. Front Immunol 12, 763292
  24. Kwok AJ, Mentzer A and Knight JC (2021) Host genetics and infectious disease: new tools, insights and translational opportunities. Nat Rev Genet 22, 137-153 https://doi.org/10.1038/s41576-020-00297-6
  25. Sakuraba A, Haider H and Sato T (2020) Population difference in allele frequency of HLA-C*05 and its correlation with COVID-19 mortality. Viruses 12, 1333
  26. Tomita Y, Ikeda T, Sato R and Sakagami T (2020) Association between HLA gene polymorphisms and mortality of COVID-19: an in silico analysis. Immun Inflamm Dis 8, 684-694 https://doi.org/10.1002/iid3.358
  27. Deng H, Yan X and Yuan L (2021) Human genetic basis of coronavirus disease 2019. Signal Transduct Target Ther 6, 344
  28. Nesterenko PA, McLaughlin J, Tsai BL et al (2021) HLA-A(*)02:01 restricted T cell receptors against the highly conserved SARS-CoV-2 polymerase cross-react with human coronaviruses. Cell Rep 37, 110167
  29. Park HJ, Kim YJ, Kim DH et al (2016) HLA allele frequencies in 5802 Koreans: varied allele types associated with SJS/TEN according to culprit drugs. Yonsei Med J 57, 118-126 https://doi.org/10.3349/ymj.2016.57.1.118
  30. Barquera R, Collen E, Di D et al (2020) Binding affinities of 438 HLA proteins to complete proteomes of seven pandemic viruses and distributions of strongest and weakest HLA peptide binders in populations worldwide. HLA 96, 277-298 https://doi.org/10.1111/tan.13956
  31. Migliorini F, Torsiello E, Spiezia F, Oliva F, Tingart M and Maffulli N (2021) Association between HLA genotypes and COVID-19 susceptibility, severity and progression: a comprehensive review of the literature. Eur J Med Res 26, 84
  32. Rambaut A, Holmes EC, O'Toole A et al (2020) A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology. Nat Microbiol 5, 1403-1407 https://doi.org/10.1038/s41564-020-0770-5
  33. Khare S, Gurry C, Freitas L et al (2021) GISAID's role in pandemic response. China CDC Wkly 3, 1049-1051 https://doi.org/10.46234/ccdcw2021.255
  34. Kolin DA, Kulm S and Elemento O (2020) Clinical and genetic characteristics of COVID-19 patients from UK Biobank. medRxiv 2020.05.05.20075507 2020.05.05.20075507
  35. Kolin DA, Kulm S, Christos PJ and Elemento O (2020) Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. PLoS One 15, e0241264
  36. Choi H and Shin EC (2022) Hyper-inflammatory responses in COVID-19 and anti-inflammatory therapeutic approaches. BMB Rep 55, 11-19 https://doi.org/10.5483/BMBRep.2022.55.1.152
  37. Tian Y, Carpp LN, Miller HER, Zager M, Newell EW and Gottardo R (2022) Single-cell immunology of SARS-CoV-2 infection. Nat Biotechnol 40, 30-41 https://doi.org/10.1038/s41587-021-01131-y
  38. Wei J, Stoesser N, Matthews PC et al (2021) Antibody responses to SARS-CoV-2 vaccines in 45,965 adults from the general population of the United Kingdom. Nat Microbiol 6, 1140-1149 https://doi.org/10.1038/s41564-021-00947-3
  39. Kayaaslan B and Guner R (2021) COVID-19 and the liver: a brief and core review. World J Hepatol 13, 2013-2023 https://doi.org/10.4254/wjh.v13.i12.2013
  40. Maiese A, Manetti AC, La Russa R et al (2021) Autopsy findings in COVID-19-related deaths: a literature review. Forensic Sci Med Pathol 17, 279-296 https://doi.org/10.1007/s12024-020-00310-8