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| Name | Class |
|---|---|
| Faculdade da PolÃcia Militar, Goiânia, GO - Brazil | UNKNOWN |
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Various observational studies have reported an association between influenza vaccination and lower rates of infection with SARS-Cov-2 and less COVID-19 disease severity have been reported in large epidemiological studies in US, Brazil and Italy. Observational studies from the Netherlands showed also strongly reduced COVID-19 infection rates among influenza-vaccinated healthcare workers, with ORs of 0.61 and 0.49 for the first and second wave of COVID-19, respectively. In addition, in-vitro immunological analyses showed that the quadrivalent inactivated influenza vaccine can induce a trained immunity program against SARS-CoV-2 (2). In-vivo vaccination against influenza was also shown to induce improved interferon responses against SARS-CoV-2, with modulation of hyperinflammatory responses. Trained immunity could be the underlying mechanism for the potential protective effect of influenza vaccine, a mechanism that has also been proven for BCG vaccination, and epidemiological evidence suggests similar non-specific effects of MMR and OPV vaccination. Currently, various clinical trials are being conducted to study the impact of BCG, MMR and OPV vaccination on COVID-19, but prospective clinical data on influenza vaccination are lacking. Although specific COVID-19 vaccines have been developed and are proven effective, there are important reasons for assessing in a controlled randomized trial the effect of influenza and MMR vaccine on COVID19:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | sterile 0.9% NaCl |
|
| Influenza | Experimental | Influenza (tetravalent vaccine) |
|
| MMR | Experimental | measles, mumps, and rubella vaccine |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Influenza | Biological | Influenza: 0.5 ml of reconstituted Influenza vaccine will be administered intramuscularly in the left upper arm as recommended by the manufacturer. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative incidence of SARS-CoV-2 infection during 1 year follow up | COVID-19 will be defined as meeting the following two criteria:
| 3 months after inclusion |
| Cumulative incidence of SARS-CoV-2 infection | COVID-19 will be defined as meeting the following two criteria:
| 6 months after inclusion |
| Cumulative incidence of SARS-CoV-2 infection | COVID-19 will be defined as meeting the following two criteria:
| 12 months after inclusion |
| Measure | Description | Time Frame |
|---|---|---|
| Severity of SARS-CoV-2 and the incidence of clinically relevant RTI | Cumulative incidence of hospitalization for COVID-19; Cumulative incidence of ICU admission for COVID-19; Cumulative incidence of death due to COVID-19; All parameters combined, measured as number of days or number of deaths will be used to report COVID19 severity. | 3, 6 and 12 months after inclusion |
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Inclusion Criteria:
To be eligible to participate in this study, the participant must meet the following criteria:
• Be older than 18 years old. Observation: the elderly is at risk for severe forms of COVID-19, therefore, the evidence in this age group is very relevant. However, they can also be a first priority population to receive a specific vaccine, limiting the time to follow-up on the study. In addition, influenza and MMR vaccines can lead to a lower immune system in the elderly than in young people. Therefore, it is likely that a more rational choice will be to carry out the study in a young population.
Exclusion Criteria:
Participants will not be included in the study if they present (reported by the research participants):
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| Name | Affiliation | Role |
|---|---|---|
| Mihai Netea, PhD | Radboud University Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Faculdade da PolÃcia Militar | Goiânia | Goiás | Brazil |
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| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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| ID | Term |
|---|---|
| D007252 | Influenza Vaccines |
| D022542 | Measles-Mumps-Rubella Vaccine |
| ID | Term |
|---|---|
| D014765 | Viral Vaccines |
| D014612 | Vaccines |
| D001688 | Biological Products |
| D045424 | Complex Mixtures |
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| MMR vaccines | Biological | MMR: 0.5 ml of reconstituted MMR vaccine will be administered intramuscularly in the left upper arm as recommended by the manufacturer. |
|
| Placebo | Other | Placebo: 0.5 ml of 0.9% NaCl will be administered intradermally in the left upper arm. |
|
| Severity of other respiratory tract infections (RTIs) | Cumulative incidence of hospitalization for other RTIs; Cumulative incidence of hospitalization for all infections; Cumulative incidence of death due to other infections; All parameters combined, measured as number of days or number of deaths will be used to report the severity of the infection. Cumulative incidence of hospitalization for all infections | 3, 6 and 12 months after inclusion |
| Incidence and magnitude of plasma/serum antibodies (IgA, M, G) and SARS-Cov-2-specific antibodies at the end of study | The measurement of the antibodies titers will be used together with the self informed questionnaires in order to confirm the incidence of COVID19 and/or other RTIs. | 3, 6 and 12 months after inclusion |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D017778 |
| Vaccines, Combined |
| D008458 | Measles Vaccine |
| D009108 | Mumps Vaccine |
| D012411 | Rubella Vaccine |