An updated thread on the Delta variant and the reasons for our concern. As any new variant emerges, there are three main issues that we consider: transmissibility; infection severity; and impact on pre-existing immunity (reinfection risk) & vaccine effectiveness 1/n
Firstly, based on available evidence, the Delta variant appears to be between 40% and 60% more transmissible than the Alpha variant, which has been dominant in Ireland for the last 5 months 2/n
When compared with Alpha, Delta exhibits an increased growth rate, an increased secondary attack rate, increased household transmission, and laboratory evidence of increased replication in biological systems that model the human airway 3/n
As such, because the Alpha variant was itself significantly more transmissible than the original SARS-CoV-2 virus, we can say that Delta is almost certainly at least twice as transmissible as the virus we experienced last summer 4/n
Secondly, if we look at infection severity, data from Scotland and England show an increased risk of hospitalisation among individuals infected with the Delta variant compared to Alpha. Infection with Delta roughly doubled the risk of hospitalisation 5/n
The case-fatality rate for Delta (0.3%) at this time appears to be lower than that for Alpha (2%). However, a large number of cases are still within the follow-up period, so we still have more to learn about the clinical course of disease with Delta infection 6/n
Thirdly, looking at immunity, neutralisation studies using convalescent sera show a reduction in neutralisation against Delta. However, this does not (yet at least) appear to be associated with an increase in reinfections among recovered individuals 7/n
However, we do see a reduction in vaccine effectiveness (VE) for Delta compared with Alpha against symptomatic infection, particularly after one dose. Although this is concerning, VE against Delta is high after two doses, and VE against hospitalisation is maintained 8/n
In the UK, Delta is the dominant variant, accounting for approximately 97% of cases. As a consequence, case numbers, hospitalisations, & deaths have increased in recent weeks. ECDC also predicts that Delta will be responsible for 90% of EU/EEA infections by the end of August 9/n
In Ireland, it’s likely Delta will become dominant much sooner than that. Based on S gene data from the Thermo Fisher assay, the proportion of cases due to Alpha in Ireland has declined from 91% in week 23 (beginning June 7th) to 45% in week 25 (beginning June 21st) 10/n
Alpha cases yield S gene negative results on this assay; Delta cases yield S gene positive results. Based on the transmissibility data described earlier, it is probable that the vast majority of our S gene positive cases (i.e. 55%) are Delta. This will be confirmed by WGS 11/n
This dramatic increase in the proportion of Delta over the last two weeks will almost certainly lead to Delta dominance by the middle of July, with a consequent increase in case numbers, hospitalisations, and mortality in the following weeks 12/n
However, in contrast to last summer, we now have very effective vaccines. The key is to protect each other through established public health interventions (hand hygiene, distancing, mask-wearing, managing number of contacts) while the vaccines take effect 13/n
Please remember that you are not fully vaccinated until 2 weeks after your second dose of ChAdOx1 Astra Zeneca vaccine, or 7 days after your second dose of Pfizer/BioNTech vaccine. Two doses are required for optimal protection against the Delta variant #VaccinesWork 14/14
Finally, just to acknowledge the great work by @PHE_uk in generating & sharing their data on Delta and other #SARSCoV2 variants in real time, and informing many of the tweets in this thread #ThankYou @meera_chand @SMHopkins and colleagues

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More from @CillianDeGascun

1 Jun
An introductory thread on B.1.617.2 and why we’re concerned about vaccine effectiveness (VE) against this virus. TL:DR The vaccines will work against B.1.617.2 but two doses of vaccine will be required to optimise effectiveness 1/n
The primary way of measuring likely VE (or more specifically antibody effectiveness) against a virus in the lab is the neutralisation test. In this test, we try to grow (or culture) the virus in the presence of antibodies in the laboratory 2/n
If the antibody is effective, we won’t see any growth because the virus has been ‘neutralised’. If the antibody is not effective, then we will see growth. However, it’s not a yes/no answer. There will be a range of growth from none to lots 3/n
Read 17 tweets
13 Sep 20
A short thread on PCR #SARSCoV2 There’s been a lot of discussion recently about the use of PCR (Polymerase Chain Reaction) for the diagnosis of #SARSCoV2 infection, and the interpretation of its results. 1/n
Hopefully, this thread can provide some background and context for those who are not familiar with the technique. PCR has become the cornerstone of molecular diagnostics in virology, and is, simply put, a technique for amplifying DNA (and indirectly RNA). 2/n
It can be used for straightforward detection purposes i.e. to provide a qualitative yes/no answer. Alternatively, it can be used to provide a quantitative result, i.e. to tell us how much of something is present. 3/n
Read 28 tweets
26 Jan 20
#Coronaviruses: an introductory thread/primer. #Coronaviruses are a family of viruses that cause respiratory & intestinal illness in birds, animals, and humans. #2019nCoV is the 7th coronavirus known to infect humans (#HCoV).
Four #HCoVs – OC43, 229E, HKU1 & NL63 – cause mild ‘common cold-like’ illness. All of us have probably been infected with one or more of these at some time. These 4 #HCoVs only occasionally cause serious illness 2/n
The other 2 #HCoVs#SARS & #MERS – cause severe disease. #SARS emerged in 2012 & infected about 8000 people worldwide with a case fatality rate (CFR) of about 10%. The #SARS outbreak was ultimately controlled with good infection prevention & control procedures 3/n
Read 13 tweets

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