TY - JOUR
T1 - Treatment of severe COVID-19 with convalescent plasma in Bronx, NYC
AU - Yoon, Hyunah
AU - Bartash, Rachel
AU - Gendlina, Inessa
AU - Rivera, Johanna
AU - Nakouzi, Antonio
AU - Bortz, Robert H.
AU - Wirchnianski, Ariel S.
AU - Paroder, Monika
AU - Fehn, Karen
AU - Serrano-Rahman, Leana
AU - Babb, Rachelle
AU - Sarwar, Uzma N.
AU - Haslwanter, Denise
AU - Laudermilch, Ethan
AU - Florez, Catalina
AU - Eugenia Dieterle, M.
AU - Jangra, Rohit K.
AU - Maximilian Fels, J.
AU - Tong, Karen
AU - Mariano, Margarette C.
AU - Vergnolle, Olivia
AU - Georgiev, George I.
AU - Herrera, Natalia G.
AU - Malonis, Ryan J.
AU - Quiroz, Jose A.
AU - Morano, Nicholas C.
AU - Krause, Gregory J.
AU - Sweeney, Joseph M.
AU - Cowman, Kelsie
AU - Allen, Stephanie
AU - Annam, Jayabhargav
AU - Applebaum, Ariella
AU - Barboto, Daniel
AU - Khokhar, Ahmed
AU - Lally, Brianna J.
AU - Lee, Audrey
AU - Lee, Max
AU - Malaviya, Avinash
AU - Sample, Reise
AU - Yang, Xiuyi A.
AU - Li, Yang
AU - Ruiz, Rafael
AU - Thota, Raja
AU - Barnhill, Jason
AU - Goldstein, Doctor Y.
AU - Uehlinger, Joan
AU - Garforth, Scott J.
AU - Almo, Steven C.
AU - Lai, Jonathan R.
AU - Gil, Morayma Reyes
AU - Fox, Amy S.
AU - Chandran, Kartik
AU - Wang, Tao
AU - Daily, Johanna P.
AU - Pirofski, Liise Anne
N1 - Funding Information:
HY was supported by NIH/National Center for Advancing Translational Service (NCATS) Einstein-Mon-tefiore CTSA grant number UL1TR001073. LP was supported in part by NIH grants AI 123664, AI 143453, and NCATS 3UL1TR002556-04S1 and a grant from the Mathers Foundation. K Chandran was supported in part by NIH grants U19AI142777 and R01AI32633 and a COVID-19 Pilot Award from Albert Einstein College of Medicine. JRL was supported by the NIH (R01-AI125462) and a COVID-19 Pilot Award from Albert Einstein College of Medicine. SCA was supported by R01AI145024, the Wollowick Family Foundation Chair in Multiple Sclerosis and Immunology, and Janet & Martin Spatz and the Helen & Irving Spatz Foundation. Additional support was provided by the Albert Einstein Macromolecular Therapeutics Development Facility, the Einstein-Rockefeller-CUNY Center for AIDS Research (P30AI124414), and the Albert Einstein Cancer Center (P30CA013330). JPD was supported by NIH/National Institute of Allergy and Infectious Diseases R21AI141367. MCM and GIG were supported by an NIH Predoctoral Training Program in Cellular and Molecular Biology and Genetics (T32-GM007491). KT, JAQ, RJM, RHB, and GJK were supported by an NIH/National Institute of General Medical Sciences Medical Scientist Training Program (T32-GM007288) at Albert Einstein College of Medicine. This study was supported in part by a US Department of Health and Human Services, Biomedical Advanced Research and Development Authority, grant contract 75A50120C00096, NIH/NCATS grant UL1TR002377, Schwab Charitable fund (Eric E. Schmidt, Wendy Schmidt, donors), United Health Group, National Basketball Association, Millennium Pharmaceuticals, Octopharma USA, Inc., and the Mayo Clinic. The views expressed herein are those of the author and do not reflect the position of the United States Military Academy, the Department of the Army, or the Department of Defense.
Funding Information:
of the Infectious Disease Scientific Advisory Board of Integrum Scientific, LLC. In addition, KC has a SARS-CoV-2 spike neutralization assay patent pending (US Provisional Application No. 63/048,918) and a SARS-CoV-2 spike antibody assay patent pending (US Provisional Application No. 63/072,750). JRL reports grants from Adimab LLC; grants from Integrated BioTherapeutics, Inc.; grants from Mapp Biopharmaceutical, Inc.; personal fees from Johnson & Johnson; and personal fees from Celdara Medical. In addition, JRL has a COVID-19 antibody diagnostic patent pending (US Provisional Application No. 63/058,621).
Publisher Copyright:
© 2021, Yoon et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
PY - 2021/2/22
Y1 - 2021/2/22
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85101860457&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85101860457&partnerID=8YFLogxK
U2 - 10.1172/jci.insight.142270
DO - 10.1172/jci.insight.142270
M3 - Article
C2 - 33476300
AN - SCOPUS:85101860457
SN - 2379-3708
VL - 6
JO - JCI Insight
JF - JCI Insight
IS - 4
M1 - e142270
ER -