Neutralizing Power of Anti-SARS-CoV-2 (Anti-COVID-19) Serum Antibodies (PNAS)

November 15, 2024 updated by: Centre Hospitalier Régional d'Orléans

Study of the Neutralizing Power of Anti-SARS-CoV-2 (Anti-COVID-19) Serum Antibodies

Natural infection, vaccines and treatments (like monoclonal antibodies) lead to the appearance of a neutralizing power in the serum (due to induced or injected antibodies). This neutralizing power is recognized as a correlate of protection against a (new) infection. This study aims to measure the neutralizing power of the serum of patients (whether or not they have been infected with SARS-CoV-2) according to the treatments and/or vaccines received and to assess the durability of this power in the time.

Study Overview

Status

Terminated

Detailed Description

Infection, vaccines and treatments (like monoclonal antibodies) lead to the appearance of a neutralizing power in the serum (due to induced or injected antibodies). This neutralizing power is recognized as a correlate of protection against (new) infection. The purpose of this study is to measure the neutralizing power of the serum of patients (whether or not they have been infected with SARS-CoV-2) depending on the treatments and/or vaccines received and to assess the durability of this power over time.

The main objective is to measure and describe the evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies (vaccines - whatever the mode of action -, monoclonal antibodies).

The secondary objectives are:

  • to measure and describe the antibody response at the level of the nasal mucosa (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies, collected by means of a nasal swab) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies SARS-CoV-2.
  • to describe the incidence of COVID in the study patients.

Study Type

Interventional

Enrollment (Actual)

9

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Orléans, France, 45000
        • Centre Hospitalier Régional d'Orléans, France

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Adult volunteers for the study, having received or about to receive any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies (vaccines - whatever the mode of action -, monoclonal antibodies).
  • Having given their consent to participate in the study

Exclusion Criteria:

  • Minors
  • Pregnant women
  • Persons under tutorship or curatorship
  • Protected adults
  • Person under legal protection
  • Person not affiliated to a social security scheme
  • Persons unable to express their consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Group with collection of biological samples
All participants will have at each of the visits: a venipuncture sample of 2 dry tubes of 7 mL to make up 3 aliquots and a nasopharyngeal swab (optional). The aliquots of serum / plasma and the nasopharyngeal swab will be stored at -80°C until sent to the Pasteur Institute.
All participants will have at each of the visits: a venipuncture sample of 2 dry tubes of 7 mL to make up 3 aliquots and a nasopharyngeal swab (optional). The aliquots of serum / plasma and the nasopharyngeal swab will be stored at -80°C until sent to the Pasteur Institute.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evolution of the serum humoral response
Time Frame: Day 0

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 0
Evolution of the serum humoral response
Time Frame: Day 0

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 0
Evolution of the serum humoral response
Time Frame: Day 3

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 3
Evolution of the serum humoral response
Time Frame: Day 3

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 3
Evolution of the serum humoral response
Time Frame: Day 15

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 15
Evolution of the serum humoral response
Time Frame: Day 15

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 15
Evolution of the serum humoral response
Time Frame: Month 1

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 1
Evolution of the serum humoral response
Time Frame: Month 1

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 1
Evolution of the serum humoral response
Time Frame: Month 2

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 2
Evolution of the serum humoral response
Time Frame: Month 2

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 2
Evolution of the serum humoral response
Time Frame: Month 3

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 3
Evolution of the serum humoral response
Time Frame: Month 3

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 3
Evolution of the serum humoral response
Time Frame: Month 4

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 4
Evolution of the serum humoral response
Time Frame: Month 4

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 4
Evolution of the serum humoral response
Time Frame: Month 5

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 5
Evolution of the serum humoral response
Time Frame: Month 5

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 5
Evolution of the serum humoral response
Time Frame: Month 6

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 6
Evolution of the serum humoral response
Time Frame: Month 6

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 6
Evolution of the serum humoral response
Time Frame: Month 9

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 9
Evolution of the serum humoral response
Time Frame: Month 9

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 9
Evolution of the serum humoral response
Time Frame: Month 12

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 12
Evolution of the serum humoral response
Time Frame: Month 12

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 12
Evolution of the serum humoral response
Time Frame: Month 18

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 18
Evolution of the serum humoral response
Time Frame: Month 18

Evolution of the serum humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 18

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evolution of the mucosal humoral response
Time Frame: Day 0

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 0
Evolution of the mucosal humoral response
Time Frame: Day 0

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 0
Evolution of the mucosal humoral response
Time Frame: Day 3

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 3
Evolution of the mucosal humoral response
Time Frame: Day 3

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 3
Evolution of the mucosal humoral response
Time Frame: Day 15

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Day 15
Evolution of the mucosal humoral response
Time Frame: Day 15

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Day 15
Evolution of the mucosal humoral response
Time Frame: Month 1

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 1
Evolution of the mucosal humoral response
Time Frame: Month 1

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 1
Evolution of the mucosal humoral response
Time Frame: Month 2

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 2
Evolution of the mucosal humoral response
Time Frame: Month 2

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 2
Evolution of the mucosal humoral response
Time Frame: Month 3

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 3
Evolution of the mucosal humoral response
Time Frame: Month 3

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 3
Evolution of the mucosal humoral response
Time Frame: Month 4

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 4
Evolution of the mucosal humoral response
Time Frame: Month 4

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 4
Evolution of the mucosal humoral response
Time Frame: Month 5

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 5
Evolution of the mucosal humoral response
Time Frame: Month 5

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 5
Evolution of the mucosal humoral response
Time Frame: Month 6

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 6
Evolution of the mucosal humoral response
Time Frame: Month 6

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 6
Evolution of the mucosal humoral response
Time Frame: Month 9

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 9
Evolution of the mucosal humoral response
Time Frame: Month 9

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 9
Evolution of the mucosal humoral response
Time Frame: Month 12

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 12
Evolution of the mucosal humoral response
Time Frame: Month 12

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 12
Evolution of the mucosal humoral response
Time Frame: Month 18

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Flow in BAU/ml (Binding Antibody Unit/milliliter)

Month 18
Evolution of the mucosal humoral response
Time Frame: Month 18

Evolution of the mucosal humoral response (titer and neutralizing capacity of anti-SARS-CoV-2 antibodies) following any intervention inducing or conferring neutralizing anti-SARS-CoV-2 antibodies.

S-Fuse in ED50 (Effective Dilution 50% titers)

Month 18
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Day 0
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Day 0
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Day 3
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Day 3
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Day 15
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Day 15
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 1
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 1
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 2
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 2
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 3
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 3
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 4
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 4
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 5
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 5
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 6
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 6
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 9
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 9
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 12
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 12
Proportion of participants developing COVID-19 infection after these treatments
Time Frame: Month 18
Proportion of participants developing COVID-19 infection after these treatments documented (by specific PCR) SARS-CoV-2 infection.
Month 18

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Thierry PRAZUCK, Dr, CHR d'Orléans

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2022

Primary Completion (Actual)

March 16, 2023

Study Completion (Actual)

March 16, 2023

Study Registration Dates

First Submitted

March 16, 2022

First Submitted That Met QC Criteria

March 30, 2022

First Posted (Actual)

April 7, 2022

Study Record Updates

Last Update Posted (Estimated)

November 19, 2024

Last Update Submitted That Met QC Criteria

November 15, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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