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Treatment of COVID-19 with convalescent plasma: lessons from past coronavirus outbreaks
Denise J Wooding1, Horacio Bach2
1Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Insights
Convalescent plasma shows potential benefits for treating coronavirus disease 2019 (COVID-19), but more rigorous research is needed. Early administration may improve outcomes, though donor and patient selection remain unclear.
Area of Science:
- * Infectious Diseases
- * Virology
- * Hematology
Background:
- * No definitive treatment exists for COVID-19.
- * Convalescent plasma has been utilized for SARS, MERS, and COVID-19.
- * Previous pandemics saw its use in treating viral infections.
Purpose of the Study:
- * To review literature and trials on convalescent plasma efficacy for coronaviruses.
- * To assess safety, feasibility, and donor/patient selection for COVID-19 treatment.
- * To summarize evidence for convalescent plasma in treating SARS-CoV, MERS-CoV, and SARS-CoV-2.
Main Methods:
- * PubMed literature review conducted July 13, 2020.
- * Searched WHO International Clinical Trials Registry and clinicaltrials.gov.
- * Focused on human studies and registered randomized clinical trials for COVID-19.
Main Results:
- * Sixteen COVID-19, four MERS, and five SARS reports analyzed.
- * Two COVID-19 randomized trials terminated early; most reports showed potential benefit.
- * Limitations include concurrent treatments, small sample sizes, and lack of controls.
Conclusions:
- * Preliminary convalescent plasma trials suggest potential benefits for COVID-19.
- * High risk of bias in current research necessitates randomized controlled trials.
- * Efficacy and safety require further investigation through robust clinical trials.
Background:
There is currently no treatment known to alter the course of coronavirus disease 2019 (COVID-19). Convalescent plasma has been used to treat a number of infections during pandemics, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle Eastern respiratory syndrome coronavirus (MERS-CoV) and now severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).
Objectives:
To summarize the existing literature and registered clinical trials on the efficacy and safety of convalescent plasma for treating coronaviruses, and discuss issues of feasibility, and donor and patient selection.
Sources:
A review of articles published in PubMed was performed on 13 July 2020 to summarize the currently available evidence in human studies for convalescent plasma as a treatment for coronaviruses. The World Health Organization International Clinical Trials Registry and clinicaltrials.gov were searched to summarize the currently registered randomized clinical trials for convalescent plasma in COVID-19.
Content:
There were sixteen COVID-19, four MERS and five SARS reports describing convalescent plasma use in humans. There were two randomized control trials, both of which were for COVID-19 and were terminated early. Most COVID-19 reports described a potential benefit of convalescent plasma on clinical outcomes in severe or critically ill patients with few immediate adverse events. However, there were a number of limitations, including the concurrent use of antivirals, steroids and other treatments, small sample sizes, lack of randomization or control groups, and short follow-up time. Data from SARS and COVID-19 suggest that earlier administration probably yields better outcomes. The ideal candidates for recipients and donors are not known. Still, experience with previous coronaviruses tells us that antibodies in convalescent patients are probably short-lived. Patients who had more severe disease and who are earlier in their course of recovery may be more likely to have adequate titres. Finally, a number of practical challenges were identified.
Implications:
There is currently no effective treatment for COVID-19, and preliminary trials for convalescent plasma suggest that there may be some benefits. However, research to date is at high risk of bias, and randomized control trials are desperately needed to determine the efficacy and safety of this therapeutic option.
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