This is an investigator-initiated trial to evaluate the safety and efficacy of universal allogeneic anti-CD19/BCMA CAR T-cells(QT-019C) in With Relapse/Refractory Autoimmune Diseases.
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The number and severity of dose-limiting toxicity (DLT) events
Timeframe: Within 28 Days After QT-019C infusion
To evaluate the safety and tolerability of UCAR T-cell in participants with relapse/ refractory autoimmune diseases
Timeframe: 2 years
To evaluate the clinical responses and duration of UCAR-T cells in participants with relapse/ refractory autoimmune diseases
Timeframe: 2 years