2021
DOI: 10.3390/v13102050
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Rapid and Successful Implementation of a COVID-19 Convalescent Plasma Programme—The South African Experience

Abstract: Background: COVID-19 convalescent plasma (CCP) has been considered internationally as a treatment option for COVID-19. CCP refers to plasma collected from donors who have recovered from and made antibodies to SARS-CoV-2. To date, convalescent plasma has not been collected in South Africa. As other investigational therapies and vaccination were not widely accessible, there was an urgent need to implement a CCP manufacture programme to service South Africans. Methods: The South African National Blood Service and… Show more

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Cited by 5 publications
(2 citation statements)
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“…The neutralizing antibody titer is a critical parameter of CCP treatment (2,8). Many countries have developed strategies for CCP screening and defined high-titer plasma based on various serological biomarkers such as titers of neutralizing antibodies, IgG antibodies, and total antibodies (2,4,(9)(10)(11). The Clinical treatment scheme of COVID-19 convalescent plasma (pilot 3 rd edition) (12) specifies that CCP (high titer) in China should test positive after 160-fold dilution of COVID-19 serum/plasma IgG antibody or 320-fold dilution of total antibody using ELISA or chemiluminescence.…”
Section: Introductionmentioning
confidence: 99%
“…The neutralizing antibody titer is a critical parameter of CCP treatment (2,8). Many countries have developed strategies for CCP screening and defined high-titer plasma based on various serological biomarkers such as titers of neutralizing antibodies, IgG antibodies, and total antibodies (2,4,(9)(10)(11). The Clinical treatment scheme of COVID-19 convalescent plasma (pilot 3 rd edition) (12) specifies that CCP (high titer) in China should test positive after 160-fold dilution of COVID-19 serum/plasma IgG antibody or 320-fold dilution of total antibody using ELISA or chemiluminescence.…”
Section: Introductionmentioning
confidence: 99%
“…While there is some waning of antibodies, in this context we expect about 95 percent of donors who ever developed antibodies to have detectable levels at the time of testing [4] while a small proportion (we estimate in the range of 5-10 percent) of individuals who experience infection never develop detectable antibodies. [5]…”
Section: Methodsmentioning
confidence: 99%