Study Investigating the Safety of Anti-CD19 CAR-T Cells Therapy Produced at Gustave Roussy for Adults With Severe and Refractory Systemic Autoimmune Rheumatic Diseases

1. Patients ≥ 18 and ≤ 75 years of age at the time of inclusion visit.

2. ECOG Performance status 0 to 2.

3. Signed informed consent (or legal representative) must be obtained from the patient prior to participation in the study.

4. Patients must have valid health insurance coverage in the country where the study is conducted.

5. A diagnosis of treatment-refractory systemic autoimmune rheumatic disease (rheumatoid arthritis (RA), severe lupus erythematosus (SLE), Sjogren's disease (SjD), Systemic sclerosis (SSc) or idiopathic inflammatory myositis (IIM)) with a severe and progressive disease according to respective criteria below.

6. Eligible patients must have failed at least two lines of conventional or biologic immunosuppressive therapies

7. Calculated creatinine clearance (calculated using CKD-EPI 2021 Formula) \> 30 mL/min

8. Women of childbearing potential must agree to use highly effective contraception or practice true sexual abstinence for at least 1 month before study start and until 12 months after CAR-T cells infusion. (see section 7.7 " Pregnancy and contraception ").

9. Male patients must agree to practice true sexual abstinence or use condoms from 1 month before study start until 12 months after CAR-T cells infusion. Also, it is recommended the childbearing potential female partner uses a highly effective method of contraception for the same duration (cf. section 7.7 " Pregnancy and contraception ").

10. Patients shall be eligible to undergo CAR-T cells infusion

11. Patients consents to give blood samples.

12. Patients Patients must be located within one hour's driving distance from Gustave Roussy during the first 30 days after the injection and must be accompanied, as they should not drive during these initial 30 days

Specific criteria for SLE:

1. Diagnosis of SLE according to the 2019 ACR/EULAR classification criteria.

2. Patient must be positive for at least one of the following autoantibodies at screening:

1. anti-dsDNA (above the upper limit of normal, ULN) or

2. anti-Sm (above ULN) or

3. anti-nucleosome (above ULN) or

4. anti-nuclear antibodies (ANA) and a decrease of C3 or C4

3. Active severe disease with SLEDAI-2K ≥ 6

4. Inadequate response or intolerance to at least 2 immunosuppressive treatments.

Specific criteria for IIM:

1. Confirmed or probable diagnosis of idiopathic inflammatory myopathy (IIM) according to the 2017 EULAR/ACR classification criteria, including:

1. Dermatomyositis (DM)

2. Polymyositis (PM)

3. Immune-mediated necrotizing myopathy (IMNM)

4. Antisynthetase syndrome (ASS)

2. Patient must be positive for at least one of the autoantibodies associated with IIM or anti-nuclear antibodies at screening (See, 24.3 Appendix 3 - List of Scleroderma- and Myositis-Specific Autoantibodies )

3. Active myositis at baseline, demonstrated by at least one of the following:

1. Elevated muscle enzymes (e.g., CPK \> 1.5 × upper limit of normal)

2. Manual Muscle Testing (MMT-8) score \< 142/150

3. Muscle MRI or EMG showing signs of active inflammation

4. Progressive interstitial lung disease

4. Inadequate response or intolerance to at least 2 immunosuppressive treatments.

Specific criteria for SjD:

1. Diagnosis of SjD as per 2016 ACR-EULAR criteria

2. Documented seropositivity for SSA at screening or positive anti-nuclear antibodies associated with positive rheumatoid factor

3. Active systemic disease defined as ESSDAI \>5 points

4. Refractory disease defined as inadequate response to hydroxychloroquine, glucocorticoids and oral immunosuppressive treatment, and otherwise requiring cyclophosphamide or rituximab, according to EULAR recommendations for the management of Sjogren's disease12. History of intolerance or inadequate response to rituximab or cyclophosphamide is also permitted.

Specific criteria for RA

1. RA diagnosis as per ACR/EULAR 2010 classification criteria

2. Seropositivity for anti-citrullinated protein autoantibodies (ACPA) and/or rheumatoid factor (RF) at Screening

3. Treatment according to EULAR recommendation and failure of ≥2 biologic/targeted synthetic Disease Modifying Anti Rheumatic Drug (DMARDs) after failing conventional synthetic DMARD therapy (unless contraindicated)

4. Signs suggestive of active/progressive disease, defined as meeting all two below criteria at Screening:

* At least moderate disease activity (DAS28-CRP\>3.2)

* Inflammatory activity confirmed by at least 1 swollen joints (documented by clinic or ultrasound)

Specific criteria for SSc:

1. Systemic sclerosis as per the 2013 ACR/EULAR Classification Criteria

2. CT scan evidence of interstitial lung disease

3. Severe skin involvement with mRSS\>10

4. EUSTAR AI \>2,5

5. Resistance or intolerance to at least two Disease Modifying Anti Rheumatic Drugs (DMARDs).

What this study is about