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Cytokine and Chemokine Levels in Coronavirus Disease 2019 Convalescent Plasma.
Bonny, Tania S; Patel, Eshan U; Zhu, Xianming; Bloch, Evan M; Grabowski, M Kate; Abraham, Alison G; Littlefield, Kirsten; Shrestha, Ruchee; Benner, Sarah E; Laeyendecker, Oliver; Shoham, Shmuel; Sullivan, David; Quinn, Thomas C; Casadevall, Arturo; Pekosz, Andrew; Redd, Andrew D; Tobian, Aaron A R.
  • Bonny TS; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Patel EU; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Zhu X; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Bloch EM; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Grabowski MK; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Abraham AG; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Littlefield K; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Shrestha R; Department of Epidemiology, School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Benner SE; Department of Ophthalmology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Laeyendecker O; W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Shoham S; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Sullivan D; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Quinn TC; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Casadevall A; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Pekosz A; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Redd AD; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Tobian AAR; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Open Forum Infect Dis ; 8(2): ofaa574, 2021 Feb.
Article in English | MEDLINE | ID: covidwho-1069287
ABSTRACT

BACKGROUND:

The efficacy of coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) is primarily ascribed as a source of neutralizing anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies. However, the composition of other immune components in CCP and their potential roles remain largely unexplored. This study aimed to describe the composition and concentrations of plasma cytokines and chemokines in eligible CCP donors.

METHODS:

A cross-sectional study was conducted among 20 prepandemic healthy blood donors without SARS-CoV-2 infection and 140 eligible CCP donors with confirmed SARS-CoV-2 infection. Electrochemiluminescence detection-based multiplexed sandwich immunoassays were used to quantify plasma cytokine and chemokine concentrations (n = 35 analytes). A SARS-CoV-2 microneutralization assay was also performed. Differences in the percentage of detection and distribution of cytokine and chemokine concentrations were examined by categorical groups using Fisher's exact and Wilcoxon rank-sum tests, respectively.

RESULTS:

Among CCP donors (n = 140), the median time since molecular diagnosis of SARS-CoV-2 was 44 days (interquartile range = 38-50) and 9% (n = 12) were hospitalized due to COVID-19. Compared with healthy blood donor controls, CCP donors had significantly higher plasma levels of interferon (IFN)-γ, interleukin (IL)-10, IL-15, IL-21, and macrophage-inflammatory protein-1, but lower levels of IL-1RA, IL-8, IL-16, and vascular endothelial growth factor-A (P < .0014). The distributions of plasma levels of IL-8, IL-15, and IFN-inducible protein-10 were significantly higher among CCP donors with high (≥160) versus low (<40) anti-SARS-CoV-2 neutralizing antibody titers (P < .0014). The median levels of IL-6 were significantly higher among CCP donors who were hospitalized versus nonhospitalized (P < .0014).

CONCLUSIONS:

Heterogeneity in cytokine and chemokine composition of CCP suggests there is a different inflammatory state among the CCP donors compared with SARS-CoV-2 naive, healthy blood donors.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Randomized controlled trials Language: English Journal: Open Forum Infect Dis Year: 2021 Document Type: Article Affiliation country: Ofid

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Randomized controlled trials Language: English Journal: Open Forum Infect Dis Year: 2021 Document Type: Article Affiliation country: Ofid