https://www.medrxiv.org/content/10.1101/2020.07.09.20148429v1
This article is a preprint and has not been certified by peer review [what does this mean?]. It reports new medical research that has yet to be evaluated and so should not be used to guide clinical practice.
This article is a preprint and has not been certified by peer review [what does this mean?]. It reports new medical research that has yet to be evaluated and so should not be used to guide clinical practice.
Antibody (Ab) responses to SARS-CoV-2 can be detected in
most infected individuals 10-15 days following the onset of COVID-19
symptoms. However, due to the recent emergence of this virus in the
human population it is not yet known how long these Ab responses will be
maintained or whether they will provide protection from re-infection.
Using sequential serum samples collected up to 94 days post onset of
symptoms (POS) from 65 RT-qPCR confirmed SARS-CoV-2-infected
individuals, we show seroconversion in >95% of cases and neutralizing
antibody (nAb) responses when sampled beyond 8 days POS. We demonstrate
that the magnitude of the nAb response is dependent upon the disease
severity, but this does not affect the kinetics of the nAb response.
Declining nAb titres were observed during the follow up period. Whilst
some individuals with high peak ID50 (>10,000) maintained titres >1,000 at >60 days POS, some with lower peak ID50
had titres approaching baseline within the follow up period. A similar
decline in nAb titres was also observed in a cohort of seropositive
healthcare workers from Guy′s and St Thomas′ Hospitals. We suggest that
this transient nAb response is a feature shared by both a SARS-CoV-2
infection that causes low disease severity and the circulating seasonal
coronaviruses that are associated with common colds. This study has
important implications when considering widespread serological testing,
Ab protection against re-infection with SARS-CoV-2 and the durability of
vaccine protection.
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