Systemic Lupus Erythematosus (SLE)
Conditions
Keywords
CD19, CAR-T, SLE
Brief summary
CAR-T therapy was therefore proposed and has been recently used for cancer treatment. It has been hailed for its promising remission rates after early stage clinical trials for acute lymphoblastic leukemia. However, CAR-T therapy is seldom used for autoimmune diseases. Researchers only use it for the treatment of multiple sclerosis (MS, an autoimmune disease of the central nervous system). SLE is a kind of autoimmune diseases which involving multiple systems, organs and with the present of a variety of autoantibodies. In the conventional treatment options, SLE could be treated with chemotherapy drugs or hormone drugs. But chemotherapy and hormone drugs could barely cured SLE. And now, chimeric antigen receptor modified T cell infusion maybe an effective treatment to solve these problems. The investigators use a 2nd CAR- T with the optimized hinge and transmembrane domain to treat patients with SLE. The purpose of this study is to assess the safety and efficacy of this 2nd CAR-T cells in the treatment of SLE.
Detailed description
This study is being conducted to assess anti-CD19-CAR-T cells safety and efficacy in treating patients with systemic lupus erythematosus（SLE）.The investigators constructed a 2nd CAR, using CD19 as target, using 4-1BB as co-stimulator, and optimized the spatial conformation by a suitable hinge and transmembrane domain sequences. The infusion dose is (1-10)E6 CAR positive T cells/kg, and the specific cells numbers depends on the situation of individual CAR-T cells preparation.
Interventions
DRUGcyclophosphamide
Patients receive cyclophosphamide (Cy) on day -2 and day -1 to reduce B cells. The dose is 0.5g/m2/d.
A 2nd CAR, CD19 as target protein, 4-1BB as co-stimulator, and optimized the spatial conformation by a suitable hinge & transmembrane domain sequences. Patients infused with anti-CD19-CAR-T cells transduced with lentivirus on day 0 in the absence of disease progression or unacceptable toxicity to treatment of SLE. The dose is 1E6\ 1E7 CD19-CAR positive T cells. The cells infusion process may last for 30 min.
Sponsors
RenJi Hospital
Shanghai GeneChem Co., Ltd.
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
No
Inclusion criteria
* Clinical diagnosis of systemic lupus erythematosus (SLE) patients * Patients with CD19+ B-cell SLE as confirmed by Flow Cytometry * Age: 18-69 years old * Creatinine \< 1.5 mg/dl * cardiac ejection fraction\>55% * hemoglobin\>9g/dL * Bilirubin \<2.0 mg/dl * Successful test expansion of T-cells * Adequate venous access for apheresis, and no other contraindications for leukapheresis * Voluntary informed consent is given
Exclusion criteria
* Pregnant or lactating women * Uncontrolled active infection * Concurrent use of systemic steroids. Recent or current use of inhaled steroids is not exclusionary * Previously treatment with any gene therapy products * Feasibility assessment during screening demonstrates\<5% transduction of target lymphocytes, or insufficient expansion (\<5-fold) in response to CD3/CD28 costimulation * Any serious, uncontrolled diseases (including, but not limit to, unstable angina pectoris, congestive heart failure, serious arrhythmia)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety of CAR-T cell（i.v.）by number of patients with adverse event | 6 weeks | adverse event is evaluated with CTCAE, version 4.0 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of patients with tumor response | 8 weeks | summarize tumor response by overall response rates |
| 3. Detection of transferred T cells in the circulation using quantitative -PCR | 6 weeks | — |
Countries
China
Contacts
Primary ContactQiang Guo, Doctor
Backup ContactXuejun Yu, Master
Outcome results
None listed