4.7 Article

Treatment of severe COVID-19 with convalescent plasma in Bronx, NYC

Journal

JCI INSIGHT
Volume 6, Issue 4, Pages -

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/jci.insight.142270

Keywords

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Funding

  1. NIH/National Center for Advancing Translational Service (NCATS) Einstein-Montefiore CTSA [UL1TR001073]
  2. NIH [AI 123664, AI 143453, U19AI142777, R01AI32633, R01-AI125462]
  3. Mathers Foundation
  4. COVID-19 Pilot Award from Albert Einstein College of Medicine [R01AI145024]
  5. Wollowick Family Foundation Chair in Multiple Sclerosis
  6. Helen & Irving Spatz Foundation
  7. Einstein-Rockefeller-CUNY Center for AIDS Research [P30AI124414]
  8. Albert Einstein Cancer Center [P30CA013330]
  9. NIH/National Institute of Allergy and Infectious Diseases [R21AI141367]
  10. NIH Predoctoral Training Program in Cellular and Molecular Biology and Genetics [T32-GM007491]
  11. NIH/National Institute of General Medical Sciences Medical Scientist Training Program [T32-GM007288]
  12. US Department of Health and Human Services, Biomedical Advanced Research and Development Authority [75A50120C00096]
  13. NIH/NCATS [UL1TR002377]
  14. Schwab Charitable fund
  15. United Health Group
  16. National Basketball Association
  17. Octopharma USA, Inc.
  18. Mayo Clinic
  19. Albert Einstein Macromolecular Therapeutics Development Facility

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Convalescent plasma therapy may be beneficial for COVID-19 patients, especially those under 65 years old. Pretransfusion antibody titers are associated with treatment efficacy.
Convalescent plasma with severe acute respiratory disease coronavirus 2 (SARS-CoV-2) antibodies (CCP) may hold promise as a treatment for coronavirus disease 2019 (COVID-19). We compared the mortality and clinical outcome of patients with COVID-19 who received 200 mL of CCP with a spike protein IgG titer >= 1:2430 (median 1:47,385) within 72 hours of admission with propensity score-matched controls cared for at a medical center in the Bronx, between April 13 and May 4, 2020. Matching criteria for controls were age. sex, body mass index, race, ethnicity, comorbidities, week of admission, oxygen requirement, D-dimer, lymphocyte counts, corticosteroid use, and anticoagulation use. There was no difference in mortality or oxygenation between CCP recipients and controls at day 28. When stratified by age, compared with matched controls, CCP recipients less than 65 years had 4-fold lower risk of mortality and 4-fold lower risk of deterioration in oxygenation or mortality at day 28. For CCP recipients, pretransfusion spike protein IgG, IgM, and IgA titers were associated with mortality at day 28 in univariate analyses. No adverse effects of CCP were observed. Our results suggest CCP may be beneficial for hospitalized patients less than 65 years, but data from controlled trials are needed to validate this finding and establish the effect of aging on CCP efficacy.

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