Effect of a Vaccination Against COVID-19 on Monocyte Production of Oxygenated Derivatives.

CORONAVIRUS INFECTIONS Clinical Trial

— VACTICOV2  

Official title:

How Does Vaccination Against COVID-19 Affect Monocyte Production of Oxygenated Derivatives ?

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05655351
• Other study ID #: NIMAO 2022-1
• Status: Active, not recruiting
• Phase: Early Phase 1
• Start date: December 21, 2022
• Est. completion date: March 31, 2024

Study information

• Verified date: January 2024
• Source: Centre Hospitalier Universitaire de Nimes
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Knowing that the vaccine antigen includes the ACE2 binding moiety (RBD), the hypothesis is that circulating vaccine antigen could reduce the enzymatic activity of ACE2, and thus increase circulating AngII concentration, monocyte ROS production and lymphocyte apoptosis. This hypothesis is supported by the fact that the Spike protein of SARSCoV-1, which uses the same receptor as SARS-CoV-2, induces a decrease in expression and activation of the Angiotensin II pathway in mice (Kuba et al. 2005).

Description:

In this pandemic period, vaccination against SARSCoV- 2 is an essential weapon. However, the immune memory induced by current vaccines remains ephemeral, requiring early booster shots. It is primordial to improve this vaccine memory. Recently it has been demonstrated that monocytes from certain individuals hospitalized for SARSCoV-2 infection spontaneously overproduced oxygenated derivatives (ROS) capable of inducing DNA damage in neighboring cells and T cell apoptosis (Kundura et al., 2022). In agreement with these observations, up to 50% of peripheral blood mononuclear cells (PBMC) from these patients showed DNA damage and its intensity was correlated with the percentage of apoptotic CD8+ T cells and lymphopenia. Upon entry into the target cell, SARS-CoV-2 induces the internalization of its receptor, the protease Angiotensin Converting Enzyme 2 (ACE2), which is able to degrade Angiotensin II (AngII). Consequently, the circulating level of AngII was observed to be increased in some COVID-19 patients. It was also found that AngII induced monocyte ROS production via its receptor Angiotensin receptor 1 (AT1), making monocytes capable of damaging the DNA of co-cultured cells. Moreover, the plasma level of AngII in patients correlates with the level of ROS production and the ability to damage DNA of their monocytes. The level of anti SARS-CoV-2 antibodies was shown to be inversely correlated with the level of monocyte production of ROS production during the acute phase. This suggests that the activation cascade leading to lymphopenia described could damage the specific immune memory. Now, a recent article has established the presence of circulating S1 vaccine antigen following the injection of an anti-SARS-CoV-2 vaccine with mRNA vaccine from D1 to D7 at a level of 68 ± 21 pg/mL (Ogata et al. 2022) similar to the level described in COVID-19 (Ogata et al. 2020). If the cascade of events we have identified is triggered by the circulation of the vaccine antigen, this could lead to could result in a reduced vaccine memory via lymphocyte apoptosis. Knowing that the vaccine antigen includes the ACE2 binding moiety (RBD), the hypothesis is that circulating vaccine antigen could reduce the enzymatic activity of ACE2, and thus increase circulating AngII concentration, monocyte ROS production and lymphocyte apoptosis. This hypothesis is supported by the fact that the Spike protein of SARSCoV-1, which uses the same receptor as SARS-CoV-2, induces a decrease in expression and activation of the Angiotensin II pathway in mice (Kuba et al. 2005).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: March 31, 2024
• Est. primary completion date: June 20, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Candidate for SARS-CoV-2 vaccination with an mRNA vaccine (Pfizer, Moderna).
• Subject has given free and informed consent.
• Subject who has signed the consent form.
• Person affiliated to or beneficiary of a health insurance plan.

Exclusion Criteria:

• Patients under treatment with N-acetylcysteine or sartan.
• Patients with a dysimmune pathology or immunosuppressive treatment.
• Person infected with SARS-CoV-2 within 3 months prior to inclusion.
• Person participating in a category 1 defined RIPH.
• Subject in an exclusion period as determined by another study.
• Person under court protection, guardianship or trusteeship.
• Subject who is unable to give consent.
• Subject for whom it is impossible to give clear information.
• Pregnant or breastfeeding woman.

Related Conditions & MeSH terms

• CORONAVIRUS INFECTIONS
• COVID-19

Intervention

Biological:
• anti-SARS-Cov-2 vaccination
For the purposes of the study, 10 mL of venous blood will be collected from each patient.

Locations

Country	Name	City	State
France	CHU de Nîmes, Hôpital Universitaire Caremeau	Nîmes

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

References & Publications (1)

Kundura L, Gimenez S, Cezar R, Andre S, Younas M, Lin YL, Portales P, Lozano C, Boulle C, Reynes J, Vincent T, Mettling C, Pasero P, Muller L, Lefrant JY, Roger C, Claret PG, Duvnjak S, Loubet P, Sotto A, Tran TA, Estaquier J, Corbeau P. Angiotensin II induces reactive oxygen species, DNA damage, and T-cell apoptosis in severe COVID-19. J Allergy Clin Immunol. 2022 Sep;150(3):594-603.e2. doi: 10.1016/j.jaci.2022.06.020. Epub 2022 Jul 14. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients under 30 years old before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 0
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients under 30 years old after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 7
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients under 30 years old after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 14
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients under 30 years old after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 28
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged 30 - 60 before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 0
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged 30 - 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 7
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged 30 - 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 14
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged 30 - 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (ROS) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 28
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged over 60 before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 0
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged over 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 7
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged over 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 14
Primary	Monocyte production of oxygenated derivatives (Reactive oxygen species) in patients aged over 60 after anti-SARS-CoV-2 vaccination with an mRNA vaccine.	The change (%) in the mean intensity of monocyte oxygen derivative (Reactive oxygen species) production will be measured by flow cytometry.; All data will be collected on standardized electronic clinical report form available online.; For ROS quantification: 106 PBMC will be re-suspended in 1µM dichloro-dihydro-fluorescein acetate (DCFH-DA) for 25minutes at room temperature. Data will be acquired on a Navios flow cytometer (Beckman Coulter) from 20,000 controlled events per sample and analyzed using Kaluza software (Kundura et al. 2022, in revision).; The samples will be anonymized for blind measurement (at the Institute of Human Genetics in the team of Prof. Pierre Corbeau).	Day 28
Secondary	A) Plasma AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged under 30	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 0
Secondary	A) Plasma AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged 30 - 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 0
Secondary	A) Plasma AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged over 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 0
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged under 30	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 7
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged 30 - 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 7
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged over 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 7
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged under 30	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 14
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged 30 - 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 14
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged over 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 14
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged under 30	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 28
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged 30 - 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 28
Secondary	A) Plasma AngII level after anti-SARS-CoV-2 vaccination with an mRNA vaccine in patients aged over 60	The AngII level before anti-SARS-CoV-2 vaccination with an mRNA vaccine will be measured by ELISA assay.	Day 28
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) before anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 0
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) before anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 0
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) before anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 0
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 7
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 7
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage.	Day 7
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 14
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 14
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 14
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 28
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 28
Secondary	B) DNA lesion rate (%) and intensity in peripheral blood mononuclear cells (PBMC) 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	Immunofluorescence measurement of the amount of ?-H2AX foci in PBMC as a percentage in patients aged under 30	Day 28
Secondary	C) Rate of T cell apoptosis before anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 0
Secondary	C) Rate of T cell apoptosis before anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 0
Secondary	C) Rate of T cell apoptosis before anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 0
Secondary	C) Rate of T cell apoptosis 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 7
Secondary	C) Rate of T cell apoptosis 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 7
Secondary	C) Rate of T cell apoptosis 7 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 7
Secondary	C) Rate of T cell apoptosis 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 14
Secondary	C) Rate of T cell apoptosis 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 14
Secondary	C) Rate of T cell apoptosis 14 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 14
Secondary	C) Rate of T cell apoptosis 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged under 30	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 28
Secondary	C) Rate of T cell apoptosis 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged 30 - 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 28
Secondary	C) Rate of T cell apoptosis 28 days after anti-SARS-CoV-2 mRNA vaccination in patients aged over 60	The percentage of T cells positive for annexin V (labelled with fluorescent annexin V) will be measured by flow cytometry	Day 28
Secondary	D) Presence of lymphopenia before anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged under 30	Complete blood count. Lymphocytes will be measured as a percentage.	Day 0
Secondary	D) Presence of lymphopenia before anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged 30 - 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 0
Secondary	D) Presence of lymphopenia before anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged over 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 0
Secondary	D) Presence of lymphopenia 7 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged under 30	Complete blood count. Lymphocytes will be measured as a percentage.	Day 7
Secondary	D) Presence of lymphopenia 7 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged 30 - 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 7
Secondary	D) Presence of lymphopenia 7 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged over 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 7
Secondary	D) Presence of lymphopenia 14 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged under 30	Complete blood count. Lymphocytes will be measured as a percentage.	Day 14
Secondary	D) Presence of lymphopenia 14 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged 30 - 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 14
Secondary	D) Presence of lymphopenia 14 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged over 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 14
Secondary	D) Presence of lymphopenia 28 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged under 30	Complete blood count. Lymphocytes will be measured as a percentage.	Day 28
Secondary	D) Presence of lymphopenia 28 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged 30 - 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 28
Secondary	D) Presence of lymphopenia 28 days after anti-SARS-CoV-2 vaccination by an mRNA vaccine in patients aged over 60	Complete blood count. Lymphocytes will be measured as a percentage.	Day 28
Secondary	E) Quantification of anti-S antibodies in patients aged under 30 before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	Anti-S antibodies will be quantified by enzyme-linked immunosorbent assay (ELISA) in Antibody Units/mL	Day 0
Secondary	E) Quantification of anti-S antibodies in patients aged 30 - 60 before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	Anti-S antibodies will be quantified by enzyme-linked immunosorbent assay (ELISA) in Antibody Units/mL	Day 28
Secondary	E) Quantification of anti-S antibodies in patients aged over 60 before anti-SARS-CoV-2 vaccination with an mRNA vaccine.	Anti-S antibodies will be quantified by enzyme-linked immunosorbent assay (ELISA) in Antibody Units/mL	Day 28
Secondary	F) Constitution of a biobank	Plasma and cell samples will be referenced and stored for use in future studies.	Day 28