The statements put forward by @GVDBossche have created anxiety. @GVDBossche has invited to discussion, but few scientists seem to have replied. The lack of response seems to generate more anxiety. I have received many requests to give my take and felt obliged to do so. 1/n
First a few words on my background: I am an MD working in epidemiology/global health>27 years. Our studies show non-specific effects of vaccines on other infections #NSEvac; I therefore also did immunological vaccine studies to understand mechanisms. 2/n thelancet.com/journals/lanin…
My main interest in COVID-19 vaccines is whether these new vaccines also have #NSEvac (So far none of them have been studied for their effect on other infections). Thus, vaccine immunology is not my main area, but I do know more than most. Hence my feeling of obligation. 3/n
I have now studied the material put forward by @GVDBossche. Let me start with points of agreement. I agree with him that the innate immune system plays an important role and vaccines that are targeting the innate immune system may be crucial... 4/n
We and others are currently testing some candidates in the form of well-known live attenuated vaccines with stimulating effects on the innate immune system; BCG vaccine, oral polio vaccine and MMR vaccine. 5/n science.sciencemag.org/content/368/64…
I also agree that it could be a concern that “Stringent and widespread infection prevention measures are now increasingly compromising their innate immunity and rendering them more susceptible to symptomatic infection”. 6/n
Now to what I don't understand. @GVDBossche argues that after asymptomatic infection, people have "used up" their natural antibody, making them prone to reinfection. How used up? Normally the immune system is good at making more of what is being useful. 7/n
@GVDBossche further argues that after asymptomatic infection, people only have short-lived measurable specific antibodies of suboptimal maturity. But e.g. in Guinea-Bissau most cases were asymptomatic, but still IgG positives months after. 8/n medrxiv.org/content/10.110…
I would expect that they would respond anamnestically next time and this would protect, at least from severe disease. The fact that we have not seen a high rate of rapid reinfections one year into the pandemic supports that. 9/n linkinghub.elsevier.com/retrieve/pii/S…
Generally, @GVDBossche don't seem to count in immunity after natural infection. Most people develop good immunity, including T-cell immunity towards non-spike epitopes, i.e. presumably also towards vaccine escapes. They contribute to herd immunity.10/n pubmed.ncbi.nlm.nih.gov/33128877/
A cornerstone in the argument seems to be that an adaptive immune response weakens the innate immune response. It wouldn't be logical nor do I think we have such evidence. On the contrary many infections and vaccines train the innate immune system. 11/n nature.com/articles/s4157…
Reg. vaccines: @GVDBossche says that getting infected while having a suboptimal response after a first dose of vaccine will lead to escape mutants. Not my area, but most people argue that due to the strong protection already after first doses, this is unlikely. 12/n
@GVDBossche argues that with mass vaccination of the elderly, the more the virus "will be forced to continue causing disease in younger age groups". Also not understood. There is no fixed quota of disease; presumably the less disease - the less opportunities to get infected. 13/n
From a historical perspective, pandemics have not all been mild in children/young people and worse with increasing age (e.g. Spanish flu, swine flu). Hence, the theory that young people have more natural antibody and that protects them against disease does not seem to hold. 14/n
Bottomline: I agree with @GVDBossche that innate immunity is important, and I'm also cautious about the new vaccines (as we still don't know about their #NSEvac). But I don't follow the argument that the vaccines will breed highly infectious variants and worsen the pandemic. 15/n
PS: I have a feeling I will regret posting this thread; the debate so far has mostly been non-scientific and nasty. However, I feel responsible towards lay people who are truly concerned about the doomsday scenario and request a scientist response. Please treat me nicely🙂

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More from @StabellBenn

13 Mar
Det mener jeg også. Studiet antager, at en person, der tester positiv så lidt som een dag efter indexcase, er smittet af indexcase. Det kan skabe falsk association ml. høj CT og smitterisiko, hvis mange bare er familie ”lilla periode” - se figur.
Jeg har spurgt forfatterne, om de vil prøve med større vindue; formodningen er, at associationen mindskes. En anden måde test er ved at se på, hvor mange sekundærcases, der kom på hospital; formodningen er, at der var meget få blandt "sekundærcases" til de med højt CT.
Studiet bekræfter fund fra England og Spanien: der er flot korrelation mellem CT-værdi og smitterisiko. Det er det eneste studie, der angiver at finde smitte ved høje CT. Det kalder på grundig undersøgelse af om der kunne være fejlkilder a la ovenstående.
Read 4 tweets
12 Mar
I @Orientering (56:29): Hvis der er god dokumentation for gavn af en Corona-anbefaling (test, isolation, etc) og man gør det praktisk muligt for folk, så vil folk følge anbefalingerne. Lad os skaffe den dokumentation ved at teste vores anbefalinger. dr.dk/radio/p1/orien…
Lad os lave masser af forsøg. Fx om der er gavn af at teste asymptomatiske i ikke-udbrudssituationer - som vi nu er i gang med i stor stil - ved at lade nogle skoler have de to gange ugentlige tests, men fritage andre fra dem. linkedin.com/pulse/et-%C3%A…
Lad os teste, om vi kan forbedre smitteopsporing ved at inddrage viden om mængden af virus i prøven, og give de folk, der har meget virus i halsen, besked om, at de kan være mulige superspredere og at det er ekstra vigtigt at informere alle kontakter.
Read 5 tweets
18 Nov 20
Jeg medvirker i denne artikel, men er ikke tilfreds med, at der er kludder i begreberne. "Falsk positive" med PCR er hvis man ikke har noget virus i halsen, men alligevel testes positiv. Det er der meget lille risiko for. 1/ tjekdet.dk/faktatjek/anal…
"Funktionelt positiv" er noget andet. Det handler om, hvorvidt man har LEVENDE virus i halsen og dermed kan smitte andre. Vi ved, at jo flere "cykler" (=jo højere "CT"), jo mindre er den statistiske sandsynlighed for, at man har levende virus i halsen. 2/ medrxiv.org/content/10.110…
SSI har ikke offentliggjort CT tallene, men baseret på andre studier er der mange "funktionelt negative", altså folk der testes positive uden at kunne smitte andre. Statistisk set er de fleste asymptomatiske med høj CT nogle, der har haft infektion. 3/ nytimes.com/2020/08/29/hea…
Read 7 tweets
27 Aug 20
Skal alle danskere vaccineres mod COVID-19? Baseret på hvad vi ved, er mit svar et klart nej. Her mine tanker.:1) Diskussionen er for tidligt ude. Vi har ikke en vaccine endnu. Vi har aldrig skabt en effektiv vaccine mod Corona-virus. Vi har ventet >35 år på en HIV-vaccine.1/8
2) Hvis vi får en vaccine, ved vi ikke, hvor mange doser, der skal til for at give beskyttelse. "Ikke-levende” vacciner skal man typisk have 2-3 doser af for at opnå immunitet. 3) Vi ved ikke, hvor længe beskyttelsen varer, det kan være som influenzavaccine: en ny hvert år. 2/8
4) Baseret på ovenstående kan vi risikere at en strategi med at vaccinere alle danskere er dyr og ineffektiv. 5) Dertil kommer sikkerheden. Med en ny vaccine er der risiko for bivirkninger. Den hidtil hurtigst udviklede vaccine tog 4 år at udvikle. Her er vi under tidspres. 3/8
Read 8 tweets
22 Apr 20
ORAL POLIO VACCINE (OPV) – SOME CLARIFICATION. I’m a big OPV fan, but when I write about OPV I get negative feedback. So time to go through why I’m a fan and explain why I don’t see the same problems as some people do. Ready to get assumptions challenged? Follow this thread (1/n)
OPV was developed in the 1950s. At that time, polio was a problem. Epidemics followed epidemics, and though most people had asymptomatic disease, at its peak in the 1940s and 1950s, polio would paralyze or kill over 500,000 people worldwide every year (2/n)
After the introduction of the two polio vaccines, OPV and the inactivated polio vaccine (IPV), the incidence decreased. Cases due to wild poliovirus decreased by over 99% since 1988, from an estimated 350,000 cases then, to 33 reported cases in 2018 (3/n) who.int/en/news-room/f…
Read 22 tweets
31 Jan 20
A STORY ABOUT THE NEW #MALARIA #VACCINE.
We have written an analysis of the RTS,S malaria vaccine for @bmj_latest. In this thread, I summarise the history and describe the problems. I hope for a change of plans @WHO @WHOAFRO. bmj.com/content/368/bm…
In 2015, the RTS,S Clinical Trials Partnership published the results of a Phase-III trial of RTS,S malaria vaccine, including 6537 infants (6-12 wks) and 8922 children (5-17 mo). RTS,S gave 18% (infants)-36% (children) protection against clinical malaria. ncbi.nlm.nih.gov/pubmed/25913272
The authors wrote that there was no significant vaccine efficacy against allcause mortality". @EMA_News approved the vaccine. But based on the numbers in the appendix, we calculated that the vaccine was associated with 24% (95%CI=-3-58%) higher mortality. thelancet.com/journals/lance…
Read 17 tweets

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