Alloimmune Response to Citrullinated Shared Epitope Sequence in Patients With Rheumatoid Arthritis (ABSEC)

C

Corporacion Parc Tauli

Status

Unknown

Conditions

Rheumatoid Arthritis

Treatments

Diagnostic Test: Research new biomarker for RA

Study type

Observational

Funder types

Other

Identifiers

NCT03506035
CIR2017/011

Details and patient eligibility

About

Rheumatoid arthritis (RA) is an autoimmune and sistemic disease,characterized by joint sinovitis and the production of autoantibodies (Ab). The Ab against citrullinated peptides (ACPA) are the most specific (92-98%), and high sensitivity (75-81%) and they are of prognostic value. ACPA are already in the beginning of the disease in most cases, having been found years before its onset. Recent studies have suggested that ACPA may have a role in perpetuating inflammation, in the generation of bone erosions and in pain in RA. Citrullination is a post-translational modification mediated by the PAD, which transforms an arginine into a citrulline. In vivo, this enzyme acts in proinflammatory environments. Despite being widely studied, none of the natural citrullinated substrates have been shown to be the triggering and/or perpetuating factor in the response of B cells in RA, understanding this response as the production of ACPA. In fact, the most specific and sensitive commercial test for the detection of ACPA uses synthetic peptides protected by a patent. In the other hand, the genetic factor that most increases susceptibility to develop RA is a shared sequence of aminoacids (QKRAA, QRRAA i RRRAA), in the HLA-DRB1 gene, known as the shared epitope (SE). Also, SE, confers prognostic value, and is associated with the presence of ACPA. These SE sequences contain arginines (R), which are susceptible to be citrullinated by the PAD enzyme. We propose the hypothesis that citrullinated SE act as an antigen capable of activating the inflammatory response mediated by B and T cells in RA. The recognition of an HLA as a foreign one, would originate an answer of alloimmune type, not valued to date. The objective of the study is to test the immune response mediated by B cells and T cells, in cases and control samples, through an in vitro model that confronts them with peptides containing the citrullinated-SE sequence. In addition, we will evaluate the association between these results with the clinical features of cases (RA included in the study). Their role as a biomarker, as well as their potential to improve the tests currently available to detect ACPA will be explored.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with RA who meet 1987 ACR criteria Patients with arthritis no RA

Exclusion criteria

  • Having an intellectual disability that allows understanding the informed consent to participate in the study

Trial design

200 participants in 3 patient groups

Rheumatoid arthritis
Description:
Patients who meet the criteria of the 1987 ACR
Treatment:
Diagnostic Test: Research new biomarker for RA
Arthritis not Rheumatoid arthritis
Description:
Patients with psoriatic arthritis, peripheric spondyloarthropathies and connective tissue diseases.
Treatment:
Diagnostic Test: Research new biomarker for RA
Healthy controls
Description:
From health blood donors
Treatment:
Diagnostic Test: Research new biomarker for RA

Trial contacts and locations

0

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Central trial contact

Eduard Graell, MD. PhD

Data sourced from clinicaltrials.gov

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