TOLERA: Tolerance Enhancement in RA

Phase

Condition

Rheumatoid Arthritis

Arthritis And Arthritic Pain

Dermatomyositis (Connective Tissue Disease)

Treatment

N/A

Clinical Study ID

NCT04120831

IM101-817

Ages > 18
All Genders

Study Summary

Although anti-citrullinated protein antibodies (ACPA) including anti-CCP2 antibodies are known to promote inflammation and joint destruction in patients suffering from ACPA-positive rheumatoid arthritis, there are currently no therapies available to efficiently eliminate autoantibody production and to re-induce immune tolerance in these patients. However, both a B cell-targeting therapy (Rituximab) and a T cell targeting therapy (Abatacept) were described to lower anti-CCP2 antibody levels and occasionally trigger disappearance of these autoantibodies (sero conversion). By sequentially combining Rituximab and Abatacept, we thus aim to enhance the tolerogenic potential of these drugs and seek to eliminate autoantibody production and significantly lower ACPA titers. This would for the first time correspond to a "deep" immunological remission and a re-induction of immune tolerance.

Eligibility Criteria

Inclusion

Main inclusion criteria: Patients eligible for inclusion in this study have to fulfil all of the following criteria:

Understand and voluntarily sign an informed consent form
Male or female, age ≥ 18 years at time of consent
Able to adhere to the study visits and protocol
Satisfy the ACR-EULAR criteria of Rheumatoid Arthritis at diagnosis
SDAI≥11 at Screening
ACPA positive (anti CCP2 antibody compulsory at screening) (+/- rheumatoid factor)(≥ 40 RE/ml for CCP2 )
Completed vaccination for pneumococcus pneumoniae according to local guidelines atBaseline
Inadequate treatment response with highest tolerated dose after 3 months therapyand/or intolerance to cDMARDs specifically Methotrexate, Sulfasalazine,Hydroxychloroquine and Leflunomide or bDMARDs specifically TNF-alpha inhibitors orIL-6 receptor blockers.
Sulfasalazin, Hydroxychloroquine and Leflunomide must be stopped during screeningphase and be replaced by Methotrexate. Leflunomide must be washed out until Baseline (Colestyramine 3x/day 8g/day for 11 days).
Only simultaneous therapy with Methotrexate
Maximum Glucocorticoid dose at Baseline: 20mg Prednisolone equivalent daily
JC-Virus antibody IgG and IgM in Serum negative at screening

Exclusion

Main exclusion criteria:

Planned or ongoing pregnancy status or breast-feeding
Ongoing or previously treatment with Abatacept or Rituximab
Hypersensitivity to the active substance, mouse proteins (Rituximab), chinese hamsterovary cells (Abatacept) or other components
Use of any other biologic immunomodulatory agent (monoclonal antibody) except insulin.
Active ongoing inflammatory diseases other than RA that might confound the evaluationof the benefit of the therapy (including SLE, PSS, MCTD, SpA, Behcet disease,vasculitis or autoimmune hepatitis)
History of ongoing, chronic or recurrent infectious disease or evidence oftuberculosis infection as defined by a positive QuantiFERON TB-Gold test. If presenceof latent tuberculosis is established then treatment according to local countryguidelines must have been initiated but patient cannot take part in the study.
Known active or past infection with hepatitis B or hepatitis C at screening orbaseline as defined by Antibody positivity and/or positive DNA/RNA levels of hepatitisB/C
Uncontrolled severe concomitant disease (including diabetes with plasma glucose >11.1mmol/l rsp. 200 mg/dl, heart insufficiency >= NYHA III, COPD with severity >= GOLD 3,asthma according to GINA classification >= step 3)
Patients with weakened immune system defined as diagnosis of CVID, HIV and or totalIgG levels lower than 600 mg/dl)
Requirement for immunization with live vaccine during the study period or within 4weeks preceding baseline.
Contraindication for Rituximab or Abatacept treatment according to their SmPCs

Study Design

October 07, 2019

December 01, 2022

Study Description

Based on fact that both a B cell-targeting therapy with Rituximab and a T cell-targeting therapy with Abatacept affect ACPA levels and can occasionally induce seroconversion and an immunological remission as well immune tolerance in ACPA-positive RA patients, we conclude that T/B cell-mediated autoimmunity can be in principle reversed in RA patients suffering from active disease. We hypothesize that we can increase the tolerance-inducing potency of Rituximab and Abatacept by combining these two approaches and delivering a sequential B cell/T cell therapy with Rituximab and Abatacept. Such a combined approach might increase the rate of seroconversions in RA patients and thus re-induce tolerance in a significant number of patients which would pave the way for a long-lasting "deep immunological" and drug-free remission.

In the proposed project, we thus plan to perform a sequential treatment with initial B cell depletion with Rituximab followed by blockade of the immunological synapse by Abatacept. Such an approach aims to deplete autoreactive B cells and plasmablasts, which constitute the major source for ACPA (3) and thus reboot part of the immune system, before blocking the immunological synapse in order to enable reconstitution of self-tolerance.

Based on their recently discovered pathogenic properties and to determine a potential immunological remission in the participating RA patients, we primarily plan to evaluate the effect of a sequential Rituximab/Abatacept treatment on changes in the levels of anti CCP2 antibodies between Baseline and Week 52 and will determine the rate of seroconversions.

Secondary, we plan to perform an additional quantitative and qualitative analysis of the ACPA response. Glycosylation of ACPA was shown to modulate their inflammatory activity and is thus considered to control the onset of arthritis in ACPA-positive individuals (9). We will therefore measure glycosylation (galactosylation, fucosylation and sialylation) of ACPA and total IgG. Moreover, we plan to determine changes in total IgG, IgA and IgM subclasses, numbers of total B cells and plasmablasts as well as of CCP2-specific B cells and plasmablasts in the peripheral blood of the participating patients. The clinical outcome will be measured at week 52 described by disease activity parameters and patient questionnaires.

The longitudinal setup of this proof of concept mode of action study is to evaluate the efficacy of a subsequent Abatacept therapy post B cell depletion in regard to ACPA seroconversion, ACPA titers and B cell phenotype changes.

Connect with a study center

Universitiy Hospital Erlangen
Erlangen, Bavaria 91052
Germany
Active - Recruiting

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