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COVID-19 convalescent plasma cohort study: Evaluation of the association between both donor and recipient neutralizing antibody titers and patient outcomes.
Yokoyama, Ana Paula H; Wendel, Silvano; Bonet-Bub, Carolina; Fachini, Roberta M; Dametto, Ana Paula F; Blumm, Fernando; Dutra, Valeria F; Candelaria, Gabriela T P; Sakashita, Araci M; Machado, Rafael Rahal Guaragna; Fontão-Wendel, Rita; Hamerschlak, Nelson; Achkar, Ruth; Assunção, Murillo Santucci Cesar; Scuracchio, Patrícia; Nudelman, Victor; Pastore, Laerte; Pinho, João R R; Ben, Mirian Dal; Filho, Roberto Kalil; Marra, Alexandre R; Amano, Mariane T; Kallás, Esper G; Helito, Alfredo Salim; de Carvalho, Carlos Roberto Ribeiro; Araujo, Danielle Bastos; Durigon, Edison Luiz; Camargo, Anamaria A; Rizzo, Luiz V; Reis, Luiz F L; Kutner, Jose M.
  • Yokoyama APH; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Wendel S; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Bonet-Bub C; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Fachini RM; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Dametto APF; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Blumm F; Hospital Sírio-Libanês, Brasília, Brazil.
  • Dutra VF; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Candelaria GTP; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Sakashita AM; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Machado RRG; Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
  • Fontão-Wendel R; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Hamerschlak N; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Achkar R; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Assunção MSC; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Scuracchio P; Hospital Sírio-Libanês Blood Bank, São Paulo, Brazil.
  • Nudelman V; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Pastore L; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Pinho JRR; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Ben MD; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Filho RK; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Marra AR; University of São Paulo - Heart Institute (Incor), São Paulo, Brazil.
  • Amano MT; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Kallás EG; Office of Clinical Quality, Safety, and Performance Improvement, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
  • Helito AS; Hospital Sírio-Libanês, São Paulo, Brazil.
  • de Carvalho CRR; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Araujo DB; Department of Infectious and Parasitic Diseases, School of Medicine, University of São Paulo, São Paulo, Brazil.
  • Durigon EL; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Camargo AA; Hospital Sírio-Libanês, São Paulo, Brazil.
  • Rizzo LV; Cardio-Pulmonary Department, Pulmonary Division, Heart Institute (Incor), University of São Paulo, São Paulo, Brazil.
  • Reis LFL; Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
  • Kutner JM; Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Transfusion ; 61(8): 2295-2306, 2021 08.
Article in English | MEDLINE | ID: covidwho-1282041
ABSTRACT

BACKGROUND:

Current evidence regarding COVID-19 convalescent plasma (CCP) transfusion practices is limited and heterogeneous. We aimed to determine the impact of the use of CCP transfusion in patients with previous circulating neutralizing antibodies (nAbs) in COVID-19.

METHODS:

Prospective cohort including 102 patients with COVID-19 transfused with ABO compatible CCP on days 0-2 after enrollment. Clinical status of patients was assessed using the adapted World Health Organization (WHO) ordinal scale on days 0, 5, and 14. The nAbs titration was performed using the cytopathic effect-based virus neutralization test with SARS-CoV-2 (GenBank MT126808.1). The primary outcome was clinical improvement on day 14, defined as a reduction of at least two points on the adapted WHO ordinal scale. Secondary outcomes were the number of intensive care unit (ICU)-free days and the number of invasive mechanical ventilation-free days.

RESULTS:

Both nAbs of CCP units transfused (p < 0.001) and nAbs of patients before CCP transfusions (p = 0.028) were associated with clinical improvements by day 14. No significant associations between nAbs of patients or CCP units transfused were observed in the number of ICU or mechanical ventilation-free days. Administration of CCP units after 10 days of symptom onset resulted in a decrease in ICU-free days (p < 0.001) and mechanical ventilation-free days (p < 0.001).

CONCLUSION:

Transfusion of high titer nAbs CCP units may be a determinant in clinical strategies against COVID-19. We consider these data as useful parameters to guide future CCP transfusion practices.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Transfusion Year: 2021 Document Type: Article Affiliation country: Trf.16573

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Transfusion Year: 2021 Document Type: Article Affiliation country: Trf.16573