Background Steroid-resistant nephrotic syndrome (SRNS), commonly caused by focal segmental glomerulosclerosis (FSGS), is associated with progression to stage 5 chronic kidney disease, requirement for kidney replacement therapy and a risk of disease recurrence post-kidney transplantation. Ofatumumab (OFA) is a fully humanised monoclonal antibody to CD20, with similar mechanisms of action to rituximab (RTX). Methods We report a case series of seven UK patients (five paediatric, two adult), all of whom developed FSGS recurrence after kidney transplantation and received OFA as part of their therapeutic intervention. All also received concomitant plasmapheresis. The 2-year outcome of these seven patients is reported, describing clinical course, kidney function and proteinuria. Results Four patients (all paediatric) achieved complete urinary remission with minimal proteinuria 12 months post-treatment. Three of those four also had normal graft function. Two patients showed partial remission-brief improvement to non-nephrotic proteinuria (197 mg/mmol) in one patient, maintained improvement in kidney function (estimated glomerular filtration rate 76 ml/min/1.73 m(2)) in the other. One patient did not demonstrate any response. Conclusions OFA may represent a useful addition to therapeutic options in the management of FSGS recurrence post-transplantation, including where RTX has shown no benefit. Concomitant plasmapheresis in all patients prevents any definitive conclusion that OFA was the beneficial intervention.
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Univ Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Troost, Jonathan P.
Trachtman, Howard
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NYU Langone Hlth, Div Nephrol, Dept Pediat, New York, NY USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Trachtman, Howard
Spino, Cathie
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Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Spino, Cathie
Kaskel, Frederick J.
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Childrens Hosp Montefiore, Div Pediat Nephrol, Bronx, NY USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Kaskel, Frederick J.
Friedman, Aaron
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Univ Minnesota, Div Nephrol, Dept Pediat, Minneapolis, MN USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Friedman, Aaron
Moxey-Mims, Marva M.
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George Washington Univ, Div Nephrol, Childrens Natl Hosp, Dept Pediat,Sch Med, Washington, DC USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Moxey-Mims, Marva M.
Fine, Richard N.
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SUNY Stony Brook, Sch Med, Med Ctr, Stony Brook, NY USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Fine, Richard N.
Gassman, Jennifer J.
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Cleveland Clin, Dept Quantitat Hlth Sci, Cleveland, OH USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Gassman, Jennifer J.
Kopp, Jeffrey B.
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NIDDKD, Kidney Dis Sect, NIH, Bethesda, MD USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Kopp, Jeffrey B.
Walsh, Liron
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Goldfinch Bio, Cambridge, MA USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Walsh, Liron
Wang, Rong
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Pfizer Inc, New York, NY USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
Wang, Rong
Gipson, Debbie S.
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Univ Michigan, Div Nephrol, Dept Pediat, Ann Arbor, MI USAUniv Michigan, Michigan Inst Clin & Hlth Res, Ann Arbor, MI USA
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Univ Pittsburgh, Med Ctr Pinnacle, Dept Internal Med, 504 S Front St,Suite 3C, Harrisburg, PA 17104 USAUniv Pittsburgh, Med Ctr Pinnacle, Dept Internal Med, 504 S Front St,Suite 3C, Harrisburg, PA 17104 USA
Hansrivijit, Panupong
Ghahramani, Nasrollah
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Penn State Univ, Coll Med, Dept Med, Div Nephrol, Hershey, PA 17033 USAUniv Pittsburgh, Med Ctr Pinnacle, Dept Internal Med, 504 S Front St,Suite 3C, Harrisburg, PA 17104 USA