Rheumatoid Arthritis — DAS28 Case Study

F, age band 45–54, Germany. Anonymized 12-month tracking on the Disease Activity Score in 28 Joints. One patient's documented experience — not a predictor of any other patient's outcome.

Case snapshot
Patient profile
F, age band 45–54, Germany
Outcome scale
DAS28 (lower is better)

DAS28 follow-up over 12 months for a German patient with seropositive rheumatoid arthritis treated with an intravenous Wharton's Jelly MSC autoimmune program in Istanbul.

Important

DAS28 improvement in this case occurred against a background of optimized DMARD therapy. The case does not isolate the contribution of MSCs and is not a predictor of any other patient's outcome.

DAS28 timeline

DAS28 combines tender joint count, swollen joint count, ESR or CRP, and patient global assessment. <2.6 = remission; 2.6–3.2 = low; 3.2–5.1 = moderate; >5.1 = high disease activity.

5.4Baseline4.6Day 903.9Day 1803.7Day 365DAS28
TimepointDAS28Δ vs baseline
Baseline5.4
Day 904.6-0.8
Day 1803.9-1.5
Day 3653.7-1.7
Baseline presentation

Seropositive rheumatoid arthritis (RF+, anti-CCP+), 11 years since diagnosis. On combination DMARD therapy with methotrexate plus a biologic. Persistent moderate disease activity (DAS28 5.4) at baseline despite optimized DMARD regimen.

Protocol delivered

Intravenous Wharton's Jelly MSCs across two infusions with structured autoimmune workup (CBC, CMP, hsCRP, ESR, anti-CCP, RF, lipid and metabolic panel). All baseline DMARD therapy continued in coordination with the patient's home rheumatologist.

Structured follow-up

DAS28 captured at Days 90, 180 and 365 by the home rheumatologist. Patient reported reduced morning stiffness from ~90 minutes to ~25 minutes by Day 180 and maintained at Day 365. No DMARD escalation required in the 12-month window.

Adverse events observed

Mild fatigue for 48 hours post infusion. No infusion reaction. No new infections.

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