Rheumatoid Arthritis Clinical Trial
— SENO-COVIDOfficial title:
Deciphering a Specific Signature of the Immunosenescence Induced in COVID-19+ Patients Versus Rheumatoid Arthritis Patients
Verified date | January 2023 |
Source | University Hospital, Montpellier |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Immune aging or immunosenescence is characterized by a loss of T cell clonal diversity and a contraction of naïve T cells with proliferative capacity associated with the functional impairment of many others immune cells as well as a chronic low degree of inflammation. A restrictive T cell repertoire is likely more prone to antigen-mediated exhaustion observed during chronic viral infections. Notably, lymphopenia is the most consistent laboratory abnormality in COVID-19 infected patients and both lung-resident and circulating T cells potently up-regulate markers of T cell exhaustion. It is not clear today if the association of COVID-19 disease severity with age is mainly related with the immunosenescence of infected patients. Interestingly, T cell exhaustion and premature immunosenescence have also been observed in chronic inflammatory diseases such as rheumatoid arthritis (RA). To better understand the immunological mechanisms involved in SARS-Cov-2 pathophysiology, the investigators propose to compare the immunosenescence patterns observed during RA, aging and SARS-Cov-2 infected patients in order to design improved therapeutic interventions.
Status | Completed |
Enrollment | 43 |
Est. completion date | November 16, 2022 |
Est. primary completion date | May 16, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria for Active RA Patients: - Patients with rheumatoid arthritis (RA) meeting the 2010 ACR/EULAR diagnostic criteria - Patients in inflammatory flare of RA (DAS28 > 3.2) - Patients who have been off biological disease-modifying antirheumatic drugs (bDMARDs) or targeted synthetic antirheumatic drugs (tsDMARDs) for RA for at least 2 weeks (except for rituximab, where a delay of at least 12 months is required) - Conventional synthetic DMARDs (Methotrexate, Hydroxychloroquine, Leflunomide, Sulfasalazine) are allowed - Beneficiary of a social security system - Informed consent Inclusion Criteria for Healthy Controls: - Absence of chronic diseases and current infection - Beneficiary of a social security system - Informed consent Inclusion Criteria for COVID-19+ Patients: - Patients with ongoing SARS-Cov-2 infection (PCR+) - Patients hospitalized at D7-D14 of symptoms onset - Patients with two or more SARS-Cov-2 symptoms (including fever, cough, dyspnea, sore throat, chest pain, anosmia, diarrhea) - Membership in or beneficiary of a social security scheme - Collection of free and informed consent Exclusion Criteria for All Groups: - Subjects under 18 years of age - HIV positive patients - Diabetic patients - Morbidly obese patients (BMI > 40kg/m2) - Use of senolytic drugs in the week prior to inclusion (azithromycin, metformin, cyclosporine, JAK inhibitors) - Use of steroids in doses greater than 10 mg/day in the week prior to inclusion - Subjects unable to give consent - Pregnant, breastfeeding, or non-menopausal women not taking effective contraception - Vulnerable subjects protected by law - Subjects under guardianship or curatorship |
Country | Name | City | State |
---|---|---|---|
France | CHU Montpellier | Montpellier |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Montpellier |
France,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Results of phenotypic immunosenescence analyses of COVID-19 patients targeting 5 different immune populations (neutrophils, T lymphocytes, NK lymphocytes, B lymphocytes and monocytes). | At inclusion visit | ||
Secondary | Comparison of previous results with the results of senescence immunophenotyping in peripheral blood of a reference population with an inflammatory disease (active RA) | At inclusion visit | ||
Secondary | Comparison of previous results with the results of senescence immunophenotyping in peripheral blood of a reference population of healthy controls. | At inclusion visit | ||
Secondary | Identification of a specific gene expression of immunosenescence induced in COVID-19 patients, using transcriptomic analysis in the different immune subpopulations previously identified and specific to COVID-19 patients. | At inclusion visit |
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