Vaccination Against Influenza in Autoimmune Diseases (MAIVAX)
Primary Purpose
Autoimmune Diseases
Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Evaluation of vaccines against flu
Sponsored by
About this trial
This is an interventional treatment trial for Autoimmune Diseases focused on measuring Influenza, autoimmune diseases, vaccination, H1N1
Eligibility Criteria
Inclusion Criteria:
- Adult patients presenting autoimmune and systemic diseases,
- treating or not with steroids, and/or immunosuppressants and/or biotherapies, especially vasculitis, scleroderma, Sjogren's syndrome and systemic lupus (main groups)
Exclusion Criteria:
- Absence of informed consent
- Disease which did not responded to the above criteria
- Active infection at time of vaccination
- HIV infection
- History of Guillain-Barre syndrome
- Allergy to one component of the vaccine
Sites / Locations
- Hopital Cochin
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Evaluation of vaccines against flu
Arm Description
Evaluation of vaccines against flu
Outcomes
Primary Outcome Measures
Protection against H1N1 influenza, defined by antibody level of 1/40, measured by hemagglutination, 3 weeks after the first injection and after the second injection
Mesure of antibody level of 1/40, measured by hemagglutination, 3 weeks after the first injection and after the second injection
Secondary Outcome Measures
Antibody levels against H1N1 in the different groups of patients, defined according diseases and their treatment (comparison of patients treated by immunosuppressants or not treated)
Antibody levels against H1N1 in the different groups of patients, defined according diseases and their treatment
Number of side effects related to vaccination
Number of local side effects related to vaccination (erythema and/or pain at injection site)
Number of patients who will develop influenza despite vaccination
Number of patients who had antibodies against H1N1 before vaccination
Number of hospitalisations and deaths related to influenza
Number of flares of the autoimmune diseases that could be related to vaccination
Determine if the induction of LT-CD4 to J21-28 anti-jams is correlated to the concentrations of antibody anti-vaccines measured in 6 months
Determine if the basal concentrations of LT-CD4 anti-jam to J21-J28 are correlated to the concentrations of antibody anti-vaccines measured in 6 months
Full Information
NCT ID
NCT01065285
First Posted
October 21, 2009
Last Updated
January 5, 2016
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT01065285
Brief Title
Vaccination Against Influenza in Autoimmune Diseases
Acronym
MAIVAX
Official Title
Evaluation of Vaccination Against Influenza (Seasonal and H1N1) in Patients Presenting Systemic or Autoimmune Diseases Treated or Not With Steroids, and/or Immunosuppressant, and/or Biotherapy: an Open, Prospective Trial (MAIVAX)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
February 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The project is to evaluate immunogenicity, efficacy and tolerance of vaccination against influenza (seasonal and H1N1) in patients affected with systemic and autoimmune diseases.
Detailed Description
This prospective study concentrates on patients with vasculitis, systemic sclerosis, Sjögren's syndrome, systemic lupus erythematosus and other connective tissue diseases.
Patients responding to the inclusion criteria, will receive vaccine against seasonal influenza then, 3 weeks later, vaccine against H1N1 influenza. According to the results of ongoing trials a second injection of H1N1 vaccine has been scheduled 3 weeks later. At each consultation a blood sample will be taken to evaluate immunogenicity of vaccination. Two additional consultations have been scheduled: one month after the last vaccine administration and at 6 month, in order to evaluate the occurrence of late side effects.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autoimmune Diseases
Keywords
Influenza, autoimmune diseases, vaccination, H1N1
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
234 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Evaluation of vaccines against flu
Arm Type
Experimental
Arm Description
Evaluation of vaccines against flu
Intervention Type
Biological
Intervention Name(s)
Evaluation of vaccines against flu
Other Intervention Name(s)
Evaluation of vaccines against flu in auto-imune diseases
Intervention Description
evaluate efficacy and tolerance
Primary Outcome Measure Information:
Title
Protection against H1N1 influenza, defined by antibody level of 1/40, measured by hemagglutination, 3 weeks after the first injection and after the second injection
Description
Mesure of antibody level of 1/40, measured by hemagglutination, 3 weeks after the first injection and after the second injection
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Antibody levels against H1N1 in the different groups of patients, defined according diseases and their treatment (comparison of patients treated by immunosuppressants or not treated)
Description
Antibody levels against H1N1 in the different groups of patients, defined according diseases and their treatment
Time Frame
3 weeks
Title
Number of side effects related to vaccination
Time Frame
3 weeks
Title
Number of local side effects related to vaccination (erythema and/or pain at injection site)
Time Frame
3 weeks
Title
Number of patients who will develop influenza despite vaccination
Time Frame
3 weeks
Title
Number of patients who had antibodies against H1N1 before vaccination
Time Frame
3 weeks
Title
Number of hospitalisations and deaths related to influenza
Time Frame
3 weeks
Title
Number of flares of the autoimmune diseases that could be related to vaccination
Time Frame
3 weeks
Title
Determine if the induction of LT-CD4 to J21-28 anti-jams is correlated to the concentrations of antibody anti-vaccines measured in 6 months
Time Frame
18 months
Title
Determine if the basal concentrations of LT-CD4 anti-jam to J21-J28 are correlated to the concentrations of antibody anti-vaccines measured in 6 months
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients presenting autoimmune and systemic diseases,
treating or not with steroids, and/or immunosuppressants and/or biotherapies, especially vasculitis, scleroderma, Sjogren's syndrome and systemic lupus (main groups)
Exclusion Criteria:
Absence of informed consent
Disease which did not responded to the above criteria
Active infection at time of vaccination
HIV infection
History of Guillain-Barre syndrome
Allergy to one component of the vaccine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Loïc GUILLEVIN, MD PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital Cochin
City
Paris
ZIP/Postal Code
75014
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
22640652
Citation
Kostianovsky A, Charles P, Alves JF, Goulet M, Pagnoux C, Le Guern V, Mouthon L, Krivine A, Villiger P, Launay O, Guillevin L; French Vasculitis Study Group. Immunogenicity and safety of seasonal and 2009 pandemic A/H1N1 influenza vaccines for patients with autoimmune diseases: a prospective, monocentre trial on 199 patients. Clin Exp Rheumatol. 2012 Jan-Feb;30(1 Suppl 70):S83-9. Epub 2012 May 11.
Results Reference
result
Learn more about this trial
Vaccination Against Influenza in Autoimmune Diseases
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