COVID-19: Past infection provides 83% protection for five months but may not stop transmission ― Study

Experts in a new study said that past infection provides 83% protection for five months but may not stop transmission because people who have previously been infected with COVID-19 could still carry the virus in their nose and throat and transmit it to others.

In a new study, the researchers tested thousands of healthcare workers in Public Health England’s Siren study between 18 June and 24 November 2020. During that period, researchers detected 44 potential reinfections and 409 new infections. This equated to an 83% rate of protection from reinfection, which appeared to last for at least for five months from first becoming sick.

The research team warned, however, that early evidence from the next stage of the study suggested that some people who are themselves protected by antibodies still carry high levels of virus and could continue to infect others.

Susan Hopkins, Public Health England senior medical advisor and Siren study lead, said, “We now know that most of those who have had the virus, and developed antibodies, are protected from reinfection, but this is not total and we do not yet know how long protection lasts. Crucially, we believe people may still be able to pass the virus on.”

NHS staff who volunteered for the study were assigned to either the positive cohort (antibody positive or prior polymerase chain reaction (PCR) antibody test positive) or negative cohort (antibody negative, not previously known to be PCR antibody positive). They attended regular PCR and antibody testing (every two to four weeks) and completed fortnightly questionnaires on symptoms and exposures.

For the analysis, between 18 June and 9 November 2020, 20 787 staff (84 per cent female, 88 per cent white, median age 45.9) were included in the study, of whom 6614 (32 per cent) were assigned to the positive cohort and 14 173 (68 per cent) to the negative cohort.

By 24 November 2020, 409 new infections were detected in the negative cohort, of whom 249 (79%) were symptomatic at infection. Meanwhile, 40 (12 per cent) were asymptomatic and 28 (9 per cent) did not complete a questionnaire at the time of their symptoms.

The researchers detected 44 potential reinfections in the positive cohort, 15 (34 per cent) of which were symptomatic. Some 42 were defined as possible (two positive PCR samples 90 or more days apart, or a new PCR positive at least four weeks after an antibody-positive result), and two were defined as probable (additionally required quantitative serological data or supportive viral genomic data). This compares with 318 new PCR positive infections (249 symptomatic) and 94 antibody seroconversions in the negative cohort.

The researchers calculated that the adjusted odds ratio was 0.17 for all reinfections (95 per cent confidence interval 0.13 to 0.24) compared with PCR confirmed primary infections, equating to 83 per cent protection. The median interval between primary infection and reinfection was over 160 days.

When looking at only symptomatic cases supported by positive PCR results, the previous infection reduced the odds of reinfection by at least 90 per cent (adjusted odds ratio 0.06 with 95 per cent CI 0.03 to 0.09).

The study team stressed that these results give no insight into the effects of vaccines or the new more transmissible variant in the UK, because of the time period analysed. These factors will be considered in later stages of analysis.

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