Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Efficacy and Safety of Telitacicept in Adult IgA Vasculitis Nephropathy

View through CrossRef
Abstract Background To investigate the efficacy and safety of telitacicept in adult immunoglobulin A vasculitis nephritis (IgAVN) patients with persistent proteinuria. Methods This prospective single-arm study enrolled patients aged ≥ 18 years diagnosed with IgAVN, an eGFR > 60 mL/min/1.73m², previously received previous treatment with corticosteroids and immunosuppressants or had contraindications to the use of corticosteroids and immunosuppressants, and a 24-hour urinary protein creatinine ratio (UPCR) > 1 g/g. Patients received telitacicept 160 mg weekly for 6 months. Results A total of 13 patients were enrolled in this study, in which 7 patients were males. The mean age of patients was 35 years. The mean time since diagnosis before telitacicept treatment was 12.6 months. After 6 months of treatment with telitacicept, the mean 24-hour UPCR decreased from a baseline value of 2.9 ± 0.8 to 0.5 ± 0.3 g/g (P < 0.001). At 9 months, 12 patients (92.3%) achieved complete remission, the mean 24-hour UPCR decreased to 0.4 ± 0.1 g/g. Additionally, the renal function of patients remained stable, urinary red blood cells, blood CD4+ T cells, CD19+ B cells, Immunoglobulin levels were decreased compared with the baseline values in all patients at 9 months (P < 0.05). No severe adverse events were observed. Conclusion Additional telitacicept significantly increased the complete remission rate of IgAVN with persistent proteinuria and stabilized renal function, without serious adverse events.
Title: Efficacy and Safety of Telitacicept in Adult IgA Vasculitis Nephropathy
Description:
Abstract Background To investigate the efficacy and safety of telitacicept in adult immunoglobulin A vasculitis nephritis (IgAVN) patients with persistent proteinuria.
Methods This prospective single-arm study enrolled patients aged ≥ 18 years diagnosed with IgAVN, an eGFR > 60 mL/min/1.
73m², previously received previous treatment with corticosteroids and immunosuppressants or had contraindications to the use of corticosteroids and immunosuppressants, and a 24-hour urinary protein creatinine ratio (UPCR) > 1 g/g.
Patients received telitacicept 160 mg weekly for 6 months.
Results A total of 13 patients were enrolled in this study, in which 7 patients were males.
The mean age of patients was 35 years.
The mean time since diagnosis before telitacicept treatment was 12.
6 months.
After 6 months of treatment with telitacicept, the mean 24-hour UPCR decreased from a baseline value of 2.
9 ± 0.
8 to 0.
5 ± 0.
3 g/g (P < 0.
001).
At 9 months, 12 patients (92.
3%) achieved complete remission, the mean 24-hour UPCR decreased to 0.
4 ± 0.
1 g/g.
Additionally, the renal function of patients remained stable, urinary red blood cells, blood CD4+ T cells, CD19+ B cells, Immunoglobulin levels were decreased compared with the baseline values in all patients at 9 months (P < 0.
05).
No severe adverse events were observed.
Conclusion Additional telitacicept significantly increased the complete remission rate of IgAVN with persistent proteinuria and stabilized renal function, without serious adverse events.

Related Results

Murine IgA binding factors (IgA-BF) suppressing IgA production: characterization and target specificity of IgA-BF.
Murine IgA binding factors (IgA-BF) suppressing IgA production: characterization and target specificity of IgA-BF.
Abstract Chemical and functional properties of IgA binding factor(s) (IgA-BF) from both murine Con A-activated spleen cells and Fc gamma R+, Fc alpha R+ T hybridoma ...
Etiology of IgA nephropathy syndrome
Etiology of IgA nephropathy syndrome
Since Berger's original paper on mesangial IgA‐IgG deposition with hematuria, there have been a number of clinical and pathological studies regarding IgA immune complexes, the mech...
An evaluation of the DiaMed assays for immunoglobulin A antibodies (anti‐IgA) and IgA deficiency
An evaluation of the DiaMed assays for immunoglobulin A antibodies (anti‐IgA) and IgA deficiency
BACKGROUND: Immunoglobulin A antibodies (anti‐IgA) are rare but can cause transfusion‐associated anaphylaxis. The detection of anti‐IgA has traditionally been performed using a lab...
Antigliadin Immunoglobulin A Best in Finding Celiac Disease in Children Younger Than 18 Months of Age
Antigliadin Immunoglobulin A Best in Finding Celiac Disease in Children Younger Than 18 Months of Age
ABSTRACTObjectives:The aim was to investigate age‐dependent serum levels and occurrence of elevated celiac disease (CD)–related antibodies in young children, to define the optimal ...
An update on the nomenclature for cutaneous vasculitis
An update on the nomenclature for cutaneous vasculitis
Purpose of review Cutaneous vasculitis reflects a spectrum ranging from skin limited to severe systemic forms. To date, there is still no generally acknowledged nomencl...

Back to Top