Rheumatoid Arthritis Clinical Trial
Official title:
Study During Pregnancy of miRNAs in Rheumatoid Arthritis or Systemic Lupus Erythematosus
Rheumatoid arthritis (RA) is a systemic disease, which mainly targets joints and results in
osteoarticular destruction and serious disability. When clinical symptoms (painful and
swollen joints) occur, the innate and adaptive immune responses against self antigens have
already been largely amplified. This might explain that even when RA patients are treated
very early and aggressively, a remission of the disease can only be obtained in approximately
half of them. This proportion of remission under treatment can only be achieved using treat
to target strategies involving biologics, such as anti-TNF. Unfortunately, less than 20% of
patients remain in remission after treatment discontinuation. Thus, despite the availability
of 5 different types of biologics, there are still therapeutic unmet needs. However, a
spontaneous, drug-free decrease of disease activity can be observed in a physiological
condition, pregnancy. Although most of treatments of RA have to be discontinued during
pregnancy, a marked improvement, and sometimes remission, can be observed during pregnancy,
with frequent post-partum flares. The situation is the opposite with an increased risk of
flares in systemic lupus erythematosus (SLE), a rare systemic autoimmune disease which
generally progresses in flares-up and can affect nearly any organ (the skin, joints, kidneys,
the brain, the heart, …). The course of the disease remains unpredictable for a given
patient, and very few biomarkers are available to help clinicians to identify patients a risk
of flares. Thus, safe therapeutic options remain limited, especially in patients with serious
complications. A specific concern in SLE is the fact that the disease usually starts in women
entering their sexual and reproductive life. Even with a stable condition (i.e : lupus
without recent flares and no impaired renal or cardiac function) as it is medically
recommended before getting pregnant, up to 40% of SLE patients flare up during pregnancy.
We hypothesize disease-specific and pregnancy-induced epigenetic changes, especially those
regarding the pattern and levels of microRNAs, could explain the clinical improvement and the
risk of flares in RA and SLE, respectively. A better understanding of the underlying
mechanisms could help to identify new biomarkers, notably those predicting flares in SLE, and
therapeutic targets, by trying to mimicking or amplifying micro-RNA changes observed in RA
and targeting them in SLE.
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