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The Sclero-JAK project aims to assess the impact of a JAK1/2 inhibitor (ruxolitinib) on activation states of monocytes-derived macrophages (MDM) from systemic sclerosis (SSc) patients
Systemic sclerosis is a fibrotic and inflammatory chronic autoimmune disorder with no disease modifiying drug available to date. JAK inhibitors may represent a relevant therapeutic candidate for this disease;
The primary objective of this study is to characterize the impact of Ruxolitinib (a JAK ½ inhibitor) on the prof-fibrotic properties of MDM from SSc patients in vitro.
The primary outcome will be the concentration of CCL18 evaluate by ELISA in the condition media of MDM from SSc patients pre treated or not in vitro by ruxolitinib.
The secondary objectives :
The secondary outcomes :
ELISA of the following cytokine evaluated in the condition media of SSc MDM pre-treated or not with ruxolitinib : PDGFbb, IL-6, CXCL10, CXCL4
Membrane expression (flow cytometry) of the following markers expressed by SSc MDM pre-treated or not with ruxoltinib : CD204, CD206, CD163, CD86, CMHII, TLR4.
Evaluation of the same cytokines and membrane markers in MDM from HD exposed to serum media of SSc patients.
Variation of the effect of ruxolitinib on the primary outcome (CCL18 secreted in the condition media of MDM from SSc patients) in sub groups depending on the following characteristics :
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Systemic sclerosis patients | SSc patients according to the ACR/EULAR 2013 classification criteria |
| |
| Healthy donors | HD healthy donors from EFS (Etablissement Français du sang) |
| |
| LUPUS Patiets | Lupus patients according to the ACR 2019 classification criteria |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| biological analysis | Other | biological analysis of the Concentration of CCL18 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Concentration of CCL18 in the condition media of MDM from SSc patients | at the end of the study | through study completion, an average of 4 year |
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Inclusion Criteria:
Exclusion Criteria:
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patients with systemic sclerosis according to the ACR/EULAR 2013 classification criteria for systemic sclerosis
or Lupus patients according to the ACR 2019 classification criteria
or healthy donors
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| Name | Affiliation | Role |
|---|---|---|
| Patrick JEGO | Rennes University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rennes University Hospital | Rennes | 35033 | France |
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| ID | Term |
|---|---|
| D012595 | Scleroderma, Systemic |
| ID | Term |
|---|---|
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D012871 | Skin Diseases |
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| ID | Term |
|---|---|
| D057919 | Biological Oxygen Demand Analysis |
| ID | Term |
|---|---|
| D004784 | Environmental Monitoring |
| D004781 | Environmental Exposure |
| D004787 | Environmental Pollution |
| D011634 | Public Health |
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| D004778 |
| Environment and Public Health |
| D015980 | Public Health Practice |