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COVID-19: What can we expect from the vaccines?

What can we expect from the COVID-19 vaccines? And how do they perform compared to previously developed vaccines against other diseases? We spoke with Prof. Gilbert Massard, Director of Medical Education at the Department of Life Sciences and Medicine, who explained the benefits and the development process of vaccines.


This article was originally published by the University of Luxembourg

What is the general benefit of vaccines?

Over the last century, there have been many success stories of vaccines as a response to epidemic situations. One famous example is the life-threatening smallpox virus which was considered eradicated after a large-scale global vaccination in the 1970s.

Likewise, poliomyelitis was successfully fought by oral vaccinations in the past and has disappeared from Europe. Overall, there are many examples where vaccinations have prevented disasters in the past and present: protection against flu and pneumonia, prevention of various children’s’ diseases such as measles, rubeola, pertussis, diphtheria and others and finally against hepatitis B, prevention of tetanus, and of cervical cancer thanks to the vaccination against papilloma virus.

We cannot tell yet how long the newly developed COVID-19 vaccines protect against the disease. However, if we refer to other vaccinations against similar pathogens, it is reasonable to assume that the COVID-19 vaccines enable an efficient protection for at least several months up to a year. Regular follow-ups of the participants in the clinical trials will soon give us a more precise figure on the long-term protection which depends on the strength of immunity.

How was the efficacy of the COVID-19 vaccines of approximately 95% determined? And how does it compare to other vaccines or drugs?

Just like any other drug, the COVID-19 vaccines were tested in different stages of clinical trials first of all to ensure that they are not harmful for people. At the same time, the efficacy was tested by vaccinating half of the probands with the real vaccine whereas the other half received the standard of care. As in the present case no alternative COVID-19 vaccine was available yet, a placebo vaccination not containing the active agent was used.

Both groups were closely observed to determine the efficacy of the vaccine, while the individual probands typically did not know to which group they belong. It was shown that the number of severe cases of COVID-19 was drastically reduced in the group of people receiving the real vaccine, which ultimately determines the efficacy.

Compared to other drugs and vaccines, an efficacy of around 95% is quite excellent. There are other vaccinations, for instance against typhus or cholera, which only show an efficacy between 50 and 70% – still the benefits of these vaccination are clearly visible. Moreover, a 100% level of protection can in practical terms never be achieved, so even after a vaccination against SARS-CoV-2, some people might get infected with the virus and fall sick – but will most likely not develop a severe course anymore.

On how many people have the vaccines been tested?

The vaccines have been tested with several tens of thousands of people during the clinical trials: For the Pfizer/BioNTech vaccine, around 35,000 people and for the Moderna vaccine over 40,000 people participated in the phase 3 testing alone.

Compared to other drugs or vaccines, this is a remarkably high number as usually only several hundred up to few thousand people take part in these trials. As a matter of fact, the COVID-19 vaccines have been tested more thoroughly than many other drugs and vaccines on the market.

Yet, this was also necessary to ensure the safety of the vaccine as the probability to discover potential side effects increases with the number of participants. Still, no unexpected or severe side effects were observed since the testing started in summer 2020, except for some individuals with a proven history of anaphylaxis.

What are the effects and side effects of the COVID-19 vaccines?

When people think of vaccines, they often also think about side effects. Indeed, what is relatively frequent is some minor pain or swelling at the injection site. Around 5% of vaccinated people may also develop headache, mild fever or fatigue which usually lasts not longer than one or two days.

However, these effects are desired and entirely expected as they also indicate the activity of the immune system. Thus, they must not be confused with real complications due to the vaccination. As mentioned above, in some rare cases, severe allergic reactions have been reported which concern only 1 to 2 out of 100,000 people and can be treated. In the vaccination centres, the physicians will interrogate everybody about allergies prior to the vaccination to minimise the risk of any negative reaction.

Is it possible that long-term effects might still occur in the future?

First of all, we need to keep in mind that the time frame in which the development of the vaccination was performed is very short. Thus, we don’t have data yet on long term complications covering several years. However, it should be noted, that generally complications due to vaccination occur with few days or weeks after the vaccination. Having vaccinated several million people over the last months and starting about half a year ago, no long-term consequences have been documented. But of course, everybody who gets vaccinated in Luxembourg will be registered for follow up.

On the other hand, we know of many severe long-term effects of the COVID-19 disease itself, and they do not only affect people of the high-risk group. People who have been on intensive care often need several weeks to months until they fully recover after the infection. In addition, around 10% of all COVID-19 patients suffer from severe long-term consequences such as decreased lung function, myocarditis, renal disfunction, fibrosis, diffuse thrombosis, or simply long-lasting fatigue. It is not yet clear if these consequences of COVID-19 are reversible and who is at risk. What is clear on the other hand is that the current vaccines are able to protect from the disease and its consequences with around 95% efficacy.

Couldn’t we wait for a few months more before we start the vaccination to gather more data?

The probability of discovering negative effects of the vaccine which have been unknown so far is extremely low. Apart from the fact that delaying the vaccination would also prolong the protective and distancing measures in place, the speed of action is crucial at this stage.

We know that RNA viruses such as SARS-CoV-2 are constantly mutating which will occasionally change their properties. Although SARS-CoV-2 mutates less frequently compared to the flu, for instance, its sheer abundance all over the world also increases the absolute number of mutations.

We already saw several new variants of the virus in the UK or South Africa, with are assumed to be more infectious. In general, mutations also always bear the risk that new variants might escape the immune response build up by vaccination.

If we wait too long to vaccinate people, we might run into the danger that another mutation will appear in which the virus is no longer recognised by the antibodies that are triggered by the available vaccines.

On the positive side, the new mRNA vaccine technology allows to also react to such mutations quite fast and the vaccine can be adapted comparably easily. Still, in the worst case there might be a gap of several weeks or months during which the infection will spread again if we do not manage to get the virus under control now.

We should keep in mind that vaccination is not only a selfish behaviour to protect oneself. It is the only effective way we have to get the pandemic under control and achieve the required global immunity level of at least 70% in the population. In addition, we must consider that anyone who is hospitalised with COVID 19 pneumonia in a standard ward or in an intensive care unit will impede access to appropriate care to people suffering from other, non-COVID diseases – these hospital beds remain accessible if all of us accept vaccination.

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COVID-19: How do different vaccines work?

How do different vaccines work? And why are people reacting differently to them? These are questions we asked Prof. Paul Wilmes, microbiologist at the Luxembourg Centre for Systems Biomedicine. As a spokesperson of the Research Luxembourg COVID-19 Task Force, he follows the development of the pandemic very closely. In this interview, he provides insights on the current status of the COVID-19 vaccines.

This article was originally published by the University of Luxembourg

Can you give us an overview which COVID-19 vaccines are currently available?

In Luxembourg, there are currently two vaccines against COVID-19 available, one from Pfizer/BioNTech and one developed by Moderna. Another vaccine from AstraZeneca has been approved by the European Medicines Agency (EMA). However, there are others being tested in clinical trials at the moment, so we can expect additional COVID-19 vaccines to become available during the year.

There is also ‘Sputnik-V’, the vaccine developed in Russia, but this has so far not been approved by the EMA. Likewise, China developed a vaccine, but recent data show that this vaccine has a quite low efficiency of only around 50%, in contrast to more than 94% for the vaccines by Pfizer/BioNTech and Moderna.

What is the difference between these vaccines?

Apart from the differences in efficacy, there are different underlying mechanisms in how the vaccines work. The Chinese vaccine uses inactivated viral particles to evoke an immune response which is a classical approach still used in vaccinations against rabies and polio, but also often results in more side-effects.

Another way is to use another virus as a carrier, for example an adenovirus, to deliver parts of the genetic material of SARS-CoV-2 into the cells. This has become a standard approach for many vaccines in the past. The COVID-19 vaccines from Russia and from AstraZeneca use this approach.

A new approach which has been in development over the past decade involves bypassing the carrier-virus and injecting directly parts of the SARS-CoV-2 genetic information in the form of mRNA. A great advantage of this technology are the comparably low production costs and easy adaptability of the vaccine in the case that the virus mutates and escapes the vaccine.

The type of vaccine also determines how many doses one needs to receive in total. The currently approved vaccines require a second dose after a few weeks to achieve an optimal effect. Some vaccines which are now in the final stages of clinical development need to be administered only once to acquire immunity, which will hopefully simplify the logistics of vaccination procedures in the future.

What happens in the cells when you get vaccinated? 

Generally speaking, vaccination is an artificial way of exposing your immune system to key molecules from a pathogen against which you want to build up immunity. The immune system recognises specific protein parts of the virus which are called antigens. Such antigens can either be introduced directly during the vaccination process or by using their genetic information such as mRNA to produce the antigen within cells. However, it is important to note that only a very small part of the virus’ genetic information is brought into one’s own cells upon vaccination. It is not possible to create a virus out of these fragments and thus vaccination cannot induce the corresponding disease.

In either case, the antigen produced by the human body is then literally presented on the surface of the muscle cells around the injection site. This then triggers the immune system as the antigen is recognised as being foreign to the body.

Why do people react differently to vaccinations and why is it not 100% efficient?

Although the principal mechanism of action of a vaccine is defined, the responses in different individuals might be different. In some people, the immune system might not recognize the presented antigen as a foreign particle, and thus not raise an immune response towards it. Also, the production rate of the antigen in the cells might be lower in some people and thus not enough of it might be available to trigger the immune system.

The individual’s prior exposure to other viruses also can play a role: the immune system could potentially identify this as a viral antigen easier if the person was infected with another closely related coronavirus in the past as for instance those causing the common cold. We now know that there is some cross reactivity between different coronaviruses in terms of our immune response, so people having developed antibodies against other coronaviruses may have a different response towards SARS-CoV-2.

Yet, it is important to keep in mind that in principle everybody is susceptible to be infected by the SARS-CoV-2 virus as humankind has not been exposed to it throughout evolution. As a consequence, there is no specific and efficient immune response by default.

Is there enough vaccine available for everybody? How long will it presumably take for everyone in Luxembourg to receive the vaccination?

At the moment, there are two major bottlenecks: one is the production of the vaccine in itself and the other concerns the logistics of administration.

The manufacturers are constantly upscaling their production and also new vaccines are expected to be approved in the near future, yet at the moment the number of doses promised have not been met.

Nevertheless, to ensure an efficient vaccination procedure for everybody in Luxembourg, national vaccination centres have been opened. One of the mRNA vaccines requires storage and transport at extremely cold temperatures of -80 °C which makes the logistical efforts quite challenging and thus requires centralisation.

The European Union has negotiated the number of doses to be received from the manufacturers to distribute them equally among their member states according to population size. Thus, the absolute number of doses available in Luxembourg is lower compared to countries such as France or Germany. According to the Joint Purchasing Agreement, Luxembourg will receive 0.14% of the doses ordered by the EU, which is also the proportion of Luxemburg citizens in the EU. While this sounds low, there is a good chance to offer the vaccination to everybody in Luxembourg until the end of 2021, as far as we can tell now. However, what remains absolutely crucial is that as many people as possible will get vaccinated as fast as possible to get out of the pandemic.

What are the priority groups for vaccination and who decides when people are invited to get vaccinated?

The Luxembourg Government has decided to give the highest priority to individuals with the highest risk to be exposed to the virus and infect others or to develop a severe course of COVID-19 upon infection. This includes for example healthcare professionals in key positions as well as older age individuals or those with specific pre-existing conditions which increases the likelihood of severe medical complications linked to COVID-19. The reason behind this strategy is to minimise the number of deaths while at the same time ensuring a functioning healthcare system.

In the end, the authorities will decide when the next group of people is invited to the vaccination centre. The Government’s vaccination strategy is informed by the recommendations of the national ethics board. Recently the Government announced phase 2 of the vaccination strategy in which people over 75 years of age and those particularly vulnerable to the disease because of existing pre-conditions will be vaccinated.

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COVID-19: Why is it safe and important to get vaccinated?

At the time of this interview, two COVID-19 vaccines have been approved by the European authorities, with both of them found to be more than 94% effective. Yet, some part of the Luxembourg population is somewhat hesitant as to whether they should get vaccinated or not. Rudi Balling, Director of the Luxembourg Centre for Systems Biomedicine (LCSB) explains the question many people have been asking: “How is it possible that the vaccines were developed so fast?” 

This article was originally published by the University of Luxembourg

When the SARS-CoV-2 virus started spreading around the world in January 2020, it was clear to the scientific community that the world is faced with a new dangerous type of virus. This led to a tremendous commitment, focus of efforts and resources made available by the entire scientific community worldwide like I have never seen before and this helped a lot in developing effective vaccines.  

Also, one should not forget that vaccine development is not something new but has a history of several decades. In the case of the COVID-19, scientists could benefit from what they knew about the SARS and MERS infections in 2002 and 2012, respectively. Those are two other types of coronaviruses against which a vaccine has started to be developed for back then. The researchers therefore did not start from scratch in this but rather focused and funnelled all their resources to develop a vaccine targeting the new virus. 

How could the vaccine be properly tested in such a short time frame? 

Generally speaking, clinical testing of any vaccine is divided into subsequent phases. Usually, the manufacturer starts the final production of a vaccine only after all phases have been completed and the vaccine is approved by the authorities, to avoid a financial risk.  

Given the urgency of the COVID-19 crisis worldwide, the different processes of final testing, approval and start of production have not been caried out sequentially, but in parallel while constantly exchanging information between all parties involved. This does not mean that the quality standards have been lowered by any means. Instead, the companies were financially backed up by the authorities so they could take the risk to move ahead faster than usual. Out of many vaccines developed in parallel, the ones that have now been approved fulfil all common regulatory requirements just like all other vaccines outside a health crisis. 

In other words, are the COVID-19 vaccines which are currently on the market safe? 

Based on the tens of thousands of people that have been vaccinated so far, there is no evidence that the COVID-19 vaccines are raising any concern about safety. As for any medication, side effects may occur for some people. However, I do not see any reason why getting the COVID-19 vaccines should be any riskier than other vaccines used for many years as the same strict criteria have been imposed for approval. 

So how can the vaccination help to protect myself? 

Up to now, we know that the infection fatality rate of SARS-CoV-2 very much depends on the age of a person. Whereas elderly and other people at high risk may have a chance of 1:100 to die from the virus, this risk is somewhat lower for younger people. Yet, the chance to die from the vaccine is still several orders of magnitude lower, in the order of millions. Just from looking at these numbers, it becomes evident that a vaccination protecting you against the virus tremendously reduces infection fatality among all age groups. 

Why is it important for everyone to get vaccinated? Isn’t it sufficient to only vaccinate the elderly population? 

A vaccination against COVID-19 can be expected to reduce the level of virus transmission to some extent. In that sense, not getting vaccinated would mean to put others at a severe and potentially deadly risk. Even if one has no symptoms one might still transmit it on to his family, at school or any outings and visits. This might ultimately impose distress on the health system which then indirectly may affect people’s health. Additionally, while the consequences of getting a SARS-CoV-2 infection are not the same for everybody, it does not take away a single bit of the responsibility everybody has for our society.

In that context, the term herd immunity is often used. What does this relate to? 

The concept of herd immunity has been discussed for several decades now. Basically, it describes an indirect protection of the population due to the people who are immune and thus cannot transmit the virus any longer. 

To picture this, imagine 1,000 mouse traps closely to each other in a room. If you throw a table tennis ball randomly into the room, you will get an exponential chain reaction without being able to stop it. Now, if you start disengaging the mouse traps one after another, the probability to trigger a chain reaction will drop as the traps become too isolated. Vaccinating people follows the same principle, reducing the amount of people infectable by the virus which may lead to herd immunity. 

Although we do not know yet when such herd immunity will be achieved as this also depends on our personal behaviour and many other factors; it will be reached faster the more people will get vaccinated and become immune. 

What are in your eyes the immediate challenges we are facing in 2021? 

Well, it’s hard to predict the future, but I would assume that towards the end of the year everybody in Luxembourg will be given the possibility to get vaccinated. Still, until then it’s a race: recently, new viral strains from the UK and South Africa have been reported. Likewise, other variants might occur with time if the virus is not stopped as soon as possible.  

In the end the virus might eventually become endemic, and we will have to live with it. Hopefully by then enough people will be protected either via vaccination or overcome infection that it will not distress the health system as it does now. 

Do you have any final recommendations? 

I can only recommend everyone to get vaccinated. Personally, I would be the first to take it. By this, you are not only protecting yourself, but are taking responsibility for the people around you. All vaccines approved in the European Union have been thoroughly tested and there is no reason to assume that they are not safe in any way.

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Survey about “social distancing”: What is our average daily contact with others?

You would like to help combat the current COVID-19 crisis? Take part in this survey and help researchers to find out how our social interactions and contact patterns change during the pandemic.

Why this study? Scientists want to find out how the current pandemic affects our social behavior. Specifically, the aim is to quantify the average number of contacts in the population at different times and compare them with previous studies and results. This data is important to include in forecasts, to generate better statistics and to better understand the spread of the virus as well as the effects of different measures.

Here the link to the survey (Surveymonkey).

The survey is anonymous and takes less than 2 minutes to complete. You are asked to indicate your gender, age and nationality, but no other personal data is requested. The results of the survey can be transmitted to research institutions, statistical offices and ministries in Luxembourg for analysis.

We do this survey regularly, in order to track the change in behaviour during the different phases of the COVID-19 crisis.

Many thanks for your participation!

Author of the survey: Joël Mossong, Ardashel Latsuzbaia
Editor: FNR

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Scientists call for synchronised curbing of COVID infections in Europe

Hundreds of scientists have called on European decision-makers to take steps for a quick, synchronised and efficient reduction in the number of COVID-19 cases across Europe.

Hundreds of scientists have called on European decision-makers to take steps for a quick, synchronised and efficient reduction in the number of COVID-19 cases across Europe.

The declaration which was published in The Lancet today was signed among others by :

  • Prof. Rudi Balling, Luxembourg Centre for Systems Biomedicine (LCSB) at the University of Luxembourg
  • Dr Jean Beissel, Centre Hospitalier de Luxembourg
  • Dr Guy Berchem, Luxembourg Institute of Health
  • Dr Stefan Beyenburg, Centre Hospitalier de Luxembourg
  • Prof. Conchita D’Ambrosio, University of Luxembourg
  • Dr Isabel de la Fuente, Centre Hospitalier de Luxembourg
  • Prof. Dr Nico Diederich, Centre Hospitalier de Luxembourg
  • Prof. Enrico Glaab, LCSB at the University of Luxembourg
  • Prof. Jorge Goncalves, LCSB at the University of Luxembourg
  • Dr Pierre Kolber, Centre Hospitalier de Luxembourg
  • Dr Barbara Klink, Laboratoire National de Santé
  • Dr Monique Reiff, Centre Hospitalier de Luxembourg
  • Till Seuring, Luxembourg Institute of Socio-Economic Research
  • Prof. Reinhard Schneider, LCSB at the University of Luxembourg
  • Prof. Alexander Skupin, LCSB at the University of Luxembourg 
  • Prof. Paul Wilmes, LCSB at the University of Luxembourg 
  • Prof. Skerdilajda Zanaj, University of Luxembourg

The signatories call for firm action to reduce case numbers quickly to low levels, to keep numbers low and to devise strategies for elimination, screening, vaccination, protection of those at high risk, as well as support for those most affected by the pandemic. The declaration argues that prompt and efficient action to curb SARS-CoV-2 infections will benefit public health, society and economy.

More than 300 representatives from research centres, hospitals, public health care institutes, universities and companies from across Europe signed the declaration.

Read the full declaration (available in multiple languages) on www.containcovid-pan.eu

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Give your voice to help COVID-19 research

Luxembourg Institute of Science and Technology (LIST) is currently conducting a research project on the detection of COVID-19 via cough and voice analysis.

Luxembourg Institute of Science and Technology (LIST) currently has many areas of research regarding the COVID-19 pandemic.One intriguing direction of research is the detection of COVID-19 via cough and voice analysis to help emergency services identify critical cases needing rapid intervention.This is done with the use of artificial intelligence to detect a COVID-19 signature that can be present in voice and in coughs.

The research project currently being carried out at LIST is called CDCVA or COVID-19 Detection by Cough and Voice Analysis. While most Coronavirus diagnoses require a physical consultations, which increases the risk of infection for staff and patients, and consume significant amounts of health system resources, the CDCVA system can be done remotely.

This exciting research could eventually lead to rapid detection of COVID-19 just through a simple telephone call.

“Respiratory conditions, such as dry cough, sore throat, excessively breathy voice and dyspnoea, caused by Covid-19, can make patients’ voices distinctive, creating identifiable voice signatures, that may be discovered using our system”, explained the project leader Muhannad Ismael.

However, the project is still in the early testing phase and LIST recently launched an appeal to the public to take a five-minute survey that includes taking vocal samples via computer or smartphone microphone.

Reaching Luxembourg and beyond

Since then over 400 samples have been taken via the online survey, but more data and completed surveys the system receives, the more it can learn and improve in the battle against COVID-19.

Therefore, the move now is to not only appeal for more vocal samples in Luxembourg, but beyond the borders too, and with that in mind three more languages; Arabic Serbian and Portuguese, have been added to the list of languages the survey can be carried out in.

“We decided to add them to reach more people from around the world. The platform is now available in eight languages and we are open to adding more soon!” said Muhannad, before adding “now, our plan is to reach out the media outside Luxembourg. At the same time, we are looking at working with the health ministry to help us by informing COVID-19 patients of the survey.”

CDCVA is also supported by the Luxembourg Institute of Health and the University of Luxembourg.

Take the survey !

Would you like to take part? It’s easy and takes about five minutes to do. The survey asks you for some general information, before asking you to record saying “aaaahhh”, cough, and read a short text. Of course everything is totally anonymous. Full details are explained on the CDCVA website.

Choose link in your language

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How bad will the Covid-19 second wave be for Luxembourg’s economy?

A newly published policy brief examines Luxembourg’s macroeconomic and epidemiological prospects for 2020-2021

The Covid-19 second wave is hitting much of Europe. While this wave mostly affected young healthy people at its start, it is now spreading to older and more vulnerable segments of the population. It is thus with a weary sense of déjà vu that European citizens have been impacted by new packages of restrictions implemented to contain the virus and to prevent healthcare systems from being overwhelmed.

In theory, such restrictions induce ambiguous effects on the economy as they directly curtail market transactions but also avoid panic-driven responses. Yet, lockdown measures implemented in March and April generated mechanical and sizeable cuts in output and plunged most economies into a temporary recession. History might be repeating itself in the coming weeks and the specter of a re-confinement hangs over Luxembourg’s economy.

In a new published policy brief “How bad will the Covid-19 second wave be for Luxembourg’s economy?” co-authored by Michal Burzynski (LISER), Frédéric Docquier (LISER) Joël Machado (LISER), Ferdy Adam (STATEC) and Tom Haas (STATEC), the authors combine recent tools developed at STATEC and LISER to assess the macroeconomic impact of the second wave, to shed light on the interactions between macroeconomic and epidemiological outcomes, and to compare the implications of moderately and highly coercive sanitary measures.

The publication stems from the FNR supported ‘MODVid’ project. The project develops analytical tools to nowcast and forecast the macroeconomic, distributional and epidemiological effects of the crisis and related public health vs. economic policy responses in Luxembourg. To learn more about MODVid and discover its research outputs, follow this link.

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Predi-COVID preliminary results

The Luxembourgish cohort study shows encouraging participation rates and sees its protocol published in international peer-reviewed journal
The Predi-COVID nurse team.

Launched under the aegis of the Research Luxembourg COVID-19 Task Force on April 24th, “Predi-COVID” is a cohort study promoted by the Luxembourg Institute of Health that aims to identify the key risk factors and biomarkers associated with COVID-19 severity and comprehend the long-term health consequences of the disease. Predi-COVID will contribute to a better understanding of the heterogeneity observed in disease severity and prognosis, ultimately enabling the accurate evaluation of patients infected with SARS-CoV-2 and more personalised care recommendations. The protocol of the study was published on November 24th in the ‘British Medical Journal Open’, reinforcing the international visibility and success of this highly collaborative “Made in Luxembourg” project. 

The study goals

Predi-COVID was launched with the goal of defining which patient profiles can be associated with a more severe prognosis. The study aims to identify the clinical, epidemiological and socio-demographic characteristics, as well as specific biomarkers from both the SARS CoV-2 virus and the patient, which can help predict the way the disease will evolve in a given individual, according notably to his immune profile.

Predi-COVID and Predi-COVID-H: patient recruitment and operational aspects

The research team has been establishing a cohort of people over the age of 18 positive for SARS CoV-2. All newly diagnosed individuals in Luxembourg can participate in Predi-COVID, upon agreeing to share their data for research purposes. In parallel to Predi-COVID, the ancillary study “Predi-COVID-H” was launched to include household members of COVID-19 positive participants to study the transmission of the virus in this high-risk population. The recruitment and data/sample collection phase started on May 5th and was initially planned to last until December 2020, although an extension period until late June 2021 is being requested.

The health evolution and symptoms of the enrolled patients are followed daily through different remote digital tools, depending on whether patients are at home or at the hospital, for 14 days from the time of confirmation of diagnosis. Short additional evaluations are also performed monthly for up to 12 months, to assess potential long-term consequences of COVID-19. Innovative digital data, specifically voice recordings, is also collected as part of the study. More detailed clinical and digital data and associated biological samples is gathered from a subset of at least 200 volunteers from the Predi-COVID cohort and from 100 Predi-COVID-H participants, in order to better characterise symptoms and clearly define the different outcomes. Upon inclusion in the study and after three weeks, several biological samples — including blood, nasal and oral swabs, saliva and stool — are collected from participants to identify human and viral predictive markers.

Preliminary results: participant recruitment, data collection, symptoms and vocal biomarkers 

Since May 5th – the date of enrolment of the first participant – and as of November 10th, 1406 and 67 eligible subjects have been contacted by phone for inclusion in Predi-COVID and in Predi-COVID-H, respectively, 556 of which agreed to be included in the former and 48 in the latter. On average, participants are 39 years old.  In terms of biological samples, the team has been establishing a unique biobank to study COVID-19, already boasting 627 specimens collected during the baseline and follow-up visits. This collection includes blood, sputum, swabs, stool and hair samples.

The preliminary findings also indicate that the majority of the enrolled population experienced few or mild symptoms. The most prevalent symptoms at admission included fever (26.2% of participants), cough (23.3%), runny nose (12.2%) and sore throat (10.8%), while the most common comorbidities and risk factors include smoking (18.1% of participants), asthma (5.4%), diabetes (4.7%), chronic heart disease (3.6%) and obesity (3.3%).

Furthermore, a total of 3,290 voice recordings has been made available by 245 participants using the CoLive LIH smartphone app, with multiple recordings per person to allow the study of the evolution of voice characteristics over time. These will enable the identification of “vocal biomarkers” of frequently observed symptoms in COVID-19 patients, such as respiratory syndromes, fatigue, anxiety or negative emotions related to COVID-19, which could subsequently be used for the easy remote monitoring of patients at home.

We are delighted with the results obtained thus far. The greater the number of participants the more accurate the final results. Besides, we are now collaborating with the Centre Hospitalier de Luxembourg to envisage the inclusion of up to 100 COVID-19 positive children in Predi-COVID and up to 30 children from affected households in Predi-COVID-H”, states Prof Markus Ollert, Director of the LIH Department of Infection and Immunity and co-Principal Investigator of Predi-COVID.

We are very grateful to the Health Inspection Department of the Ministry of Health for the unwavering support and excellent collaboration throughout, which are key to the success of the study. The protocol has recently been published in a renowned international journal and will serve as the core publication to cite for all future work based on Predi-COVID data. So far, nine ancillary projects funded by the Luxembourg National Research Fund or by the European Commission’s Horizon 2020 programme are already using Predi-COVID data”, concludes Dr Guy Fagherazzi of the LIH Department of Population Health, co-Principal Investigator of Predi-COVID and first author of the publication.   

The full study protocol was published in the ‘British Medical Journal Open’ on November 24th. It is accessible here

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Large-scale testing operations: Conclusion of phase 1 and launch of phase 2

Ministry of Health to lead the second phase as of mid-September.
On Monday, September 14th, the Minister of Higher Education and Research, Claude Meisch, the Minister of Health, Paulette Lenert, and the Research Luxembourg (RL) COVID-19 Task Force held a press conference in Dudelange to officially conclude the first phase of the large-scale testing, led by the Luxembourg Institute of Health together with the Research Luxembourg community. The operations of the second phase have been handed over to the Health Directorate of the Ministry of Health and will start mid-September.

As part of the exit strategy, Luxembourg has implemented an extensive and unique nation-wide testing campaign, inviting its residents and cross-border workers to voluntarily get tested for COVID19. The aim of this large-scale testing (LST) initiative was to limit the spread of the novel SARS-CoV-2 virus by identifying positive cases early, including among asymptomatic persons, thereby breaking infection chains. At the same time, LST aims to contribute to the close monitoring of the spread of the virus among our population.

The first phase of the LST, coordinated by the Luxembourg Institute of Health (LIH), ran from 27 May until 27 July and relied on 16 ‘drive-through’ and 1 ‘walk-through’ test stations, with a maximum theoretical capacity of 20,000 tests per day. The population was divided into three main categories. The first category was composed of people exposed to a high infectious risk by their professional activity (such as healthcare professionals) whereas the second category consisted of those having resumed their professional activity or about to get back to work. The third category encompassed representative samples of the general population. The recurring testing of the contingents and the rigorous contact tracing not only aims at avoiding new infection chains but also at providing decision makers with evidence-based data.

An extension period prior to the beginning of Phase II was set up during the summer period until 15 September with the aim of monitoring the evolution of the epidemic also during the summer months with a particular accent on people coming back from holidays, those professions specifically linked to the holiday period (Horesca, seasonal workers) and the school start.

In total, 1,520,445 invitations to LST were sent, and 560,082 tests were conducted covering 307,751 Luxembourg residents, reflecting an overall participation rate of almost 50 % of the resident population.

The second phase of the LST will be coordinated by the Health Directorate of the Ministry of Health and is set to run between 16 September 2020 and March 2021, with a capacity of 53,000 tests per week. Building on the experience gained during the first phase, which showed a relatively low prevalence rate, the second phase of the strategy will narrow the focus of the tests and target specifically the population most exposed to the virus, while at the same time allowing for capacities to be adjusted in a timely manner to the evolution of the situation and over a longer period of time than the first phase. This nuanced approach will foster a more precise meshing of the population and a more efficient reactiveness. More detailed information as to this new phase of the LST will be provided by Health Minister Paulette Lenert during a press conference on 24 September.

The handover press conference, which took place at the premises of the Integrated Biobank of Luxembourg (IBBL) in Dudelange in the presence of the Minister of Higher Education and Research, Claude Meisch and the Minister of Health Paulette Lenert, brought together all relevant stakeholders including the CEOs of Research Luxembourg-member institutions, the spokespersons of the RL Task Force, members of the LST scientific advisory board and representatives of Laboratoires Réunis.

As the work of Research Luxembourg on the large-scale testing campaign draws to a close, we would like to sincerely thank all the partners who contributed to the success of this extraordinary effort, particularly Laboratoires Réunis and the staff of Research Luxembourg member institutes

Prof Ulf Nehrbass, CEO of LIH and spokesman of the RL COVID-19 Task Force.

This unparalleled initiative has been widely recognised at the international level, further strengthening the country’s reputation as a leader in public health and biomedical research

Prof Paul Wilmes from the University of Luxembourg’s Luxembourg Centre of Systems Biomedicine (LCSB), deputy spokesman of the Task Force.

The strength of our response to the pandemic lies in the tight connection between public health initiatives such as the large-scale testing and the outstanding research efforts of Luxembourg’s research institutions. This synergy plays a fundamental role in providing tangible solutions to societal issues

Claude Meisch, Minister for Higher Education and Research.

The large scale testing project has confirmed the high level of resilience, adaptability and reactiveness of our country as we face an unprecedented crisis of international dimension. It will reinforce our preparedness all along the evolution of the epidemic. The second phase will consolidate our position as a leader in large-scale testing and will be part of the government’s efforts to fight the virus, ideally until the crisis ends, while allowing for a particular attention to be put on specific target groups

Paulette Lenert, Minister of Health.

Communicated by the Ministry of Higher Education and Research, the Ministry of Health and the Luxembourg Institute of Health. Originally published on lih.lu

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Covid-19 taskforce

Use of new FFP2 masks – ensuring safety & security in large scale testing stations

In the testing stations, the safety and security of the staff collecting samples has been and is being ensured by redundant protection measures with masks and face shields. These measures are strictly respected at all times.  The compliance of these measures and quality of the material being used in that framework is being closely monitored by Laboratoire Réunis, along with their sub-contracters for the large scale testing.

The masks used on the stations were CE labeled, certified by two testing laboratories and all certificates stating compliance with security & safety requirements had been provided.  However, lab reports recently suggested that the tests of some CE masks, including the masks being used at the stations, were not accurate. 

In light of this information, additional tests have been commissioned in an independent Belgian laboratory.  The results of the test received on 3 July 2020 state that the filtration rate of the tested masks is 93.39 %, as compared to  94% required for FFP2 masks. This means there is a differential of 0,61%.

As a consequence and as a precautionary measure, all masks of this model currently being in circulation are being collected, and will no longer be used by the staff as of this afternoon, 3 July 2020 at 4:00 p.m.  Instead, employees will be given certified 3M FFP2 masks used in the national hospitals.
Regular testing of the staff members working in the stations is also part of the standard security protocol. 

Safety and security are a priority for all partners involved in the large scale testing and all measures will be taken to ensure the highest standards are being maintained.