Healthy Volunteers Clinical Trial
— R2IGHOfficial title:
Immunoglobulin Gene Rearrangement and Repair in Healthy Donors
| Verified date | October 2021 |
| Source | University Hospital, Limoges |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
B-cells ensure humoral immune response against antigens (Ag) thanks to their receptor (BCR). V(D)J rearrangement, somatic hypermutation, immunoglobulin (Ig) class switch and locus suicide recombination are mutational/recombinational processes targeting Ig loci influencing BCR expression. Study of these events is essential for B cell function analysis. Our project will provide the normal reference values using high throughput sequencing-based protocols.
| Status | Completed |
| Enrollment | 120 |
| Est. completion date | October 14, 2021 |
| Est. primary completion date | October 14, 2021 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 70 Years |
| Eligibility | Inclusion Criteria: - healthy volunteers aged between 18 and 70 - volunteers free from lymphoid hemopathy, immune deficiency and autoimmune disease. 3 categories : volunteers between 18 and 34 years of age, volunteers between 35 and 50 years of age, volunteers between 51 and 69 years of age. Exclusion Criteria: - any recent vaccination (< 4 weeks) - tumoral pathology - lymphoïd hemopathy - immune deficiency - autoimmune disease - transplanted patients - inflammatory / systemic diseases - hypersensitivity or allergies - treatments likely to modify the immune response : - calcineurin inhibitors: ciclosporin, tacrolimus -antimetabolite: azathioprine, mycophenolate mofetil / mycophenolic acid, 6-mercaptopurine, methotrexate - cyclophosphamide - antilymphocyte serum (rabbit, horse) - mTOR inhibitors: everolimus, sirolimus - anti-CD25 (anti IL2-R): basiliximab, dacliximab -belatacept (anti CD80-86) - abatacept (CTLA4-Ig) - OKT3 (Muronomab-CD3, anti-CD23) - glucocorticoids: methylprednisolone, prednisone, prednisolone. - entuzumab (anti-CD52) - rituximab, ocrelizumab (anti-CD20) - eculizumab (anti-C5) - anakinra (analogue IL1-RA) - leflunomide (dihydroorotate dehydrogenase inhibition) - bortezomib (proteasome inhibitor) - fingolimod (S1P receptor antagonist) - alentuzumab (anti CD52) - Ig G -antiTNF (etanercept, infliximab, adalimumab, certolizumab) - vedolizumab (Anti-integrin a4ß7 Ab) - ustekinumab (anti-IL12) - natalizumab (anti-integrin a4) - mitoxantrone (topoisomerase type II inhibitor) - tocilizumab (anti-IL6) |
| Country | Name | City | State |
|---|---|---|---|
| France | Limoges University Hospital | Limoges |
| Lead Sponsor | Collaborator |
|---|---|
| University Hospital, Limoges |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Frequency of use of the V, D and J genes in VDJ rearrangements | through study completion, an average of 18 months | ||
| Secondary | Percentage of HyperMutation Somatic (SHM) in VDJ regions | through study completion, an average of 18 months | ||
| Secondary | Nature of HyperMutation Somatic (SHM) | transitions and transversions | through study completion, an average of 18 months | |
| Secondary | Ig class switching (CSR) and recombination suicide of the IgH locus (LSR) junctions | number of CSR and LSR junctions | through study completion, an average of 18 months | |
| Secondary | Frequency of g class switching (CSR) and recombination suicide of the IgH locus (LSR) junctions | frequency of CSR and LSR junctions according to their structure | through study completion, an average of 18 months |
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