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Telitacicept for refractory IgA nephropathy: a case series.
Xun-Jie Ma1, Jia-Xin Liu1, Wei-Guang Yang1
1Department of Nephrology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110001, China.
Telitacicept effectively treated IgA nephropathy (IgAN) by reducing proteinuria and improving kidney function. Benefits persisted even after discontinuing the drug, offering a promising therapy for IgAN patients.
Area of Science:
- Nephrology
- Immunology
- Pharmacology
Background:
- IgA nephropathy (IgAN) is characterized by mesangial IgA deposition, driven by galactose-deficient IgA1 (Gd-IgA1) from activated B cells.
- Telitacicept targets B-cell activation, presenting a potential therapeutic strategy for IgAN.
Purpose of the Study:
- To evaluate the efficacy and safety of telitacicept in patients with refractory IgA nephropathy.
- To assess the durability of therapeutic benefits after telitacicept discontinuation.
Main Methods:
- A study involving 9 patients with refractory IgAN receiving subcutaneous telitacicept for 12 months, followed by a 6-month withdrawal period.
- Dosage: 160 mg weekly for 6 months, then 160 mg bi-weekly for 6 months.
- Laboratory data were collected throughout the 18-month follow-up (12 months treatment + 6 months withdrawal).
Main Results:
- All patients achieved complete proteinuria remission after 12 months of telitacicept therapy.
- Estimated glomerular filtration rate (eGFR) improved and remained stable post-treatment.
- Complete remission was sustained 6 months after drug withdrawal, with 6 patients discontinuing conventional IgAN treatments.
Conclusions:
- Telitacicept demonstrates significant efficacy in reducing proteinuria and enhancing kidney function in refractory IgAN.
- The observed therapeutic effects of telitacicept are durable and maintained after treatment cessation.
- Telitacicept represents a safe and effective treatment option for IgA nephropathy, potentially allowing discontinuation of other therapies.
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