Abatacept in B7-1–Positive Proteinuric Kidney Disease
Author(s) -
Chih Chuan Yu,
Alessia Fori,
Astrid Weins,
Samy Hakroush,
Dony Maiguel,
Junichiro Sageshima,
Linda Chen,
Gaetano Ciancio,
Mohd Hafeez Faridi,
Daniel Behr,
Kirk N. Campbell,
Jer Ming Chang,
Hung Chun Chen,
Jun Oh,
Christian Faul,
M. Amin Arnaout,
Paolo Fiorina,
Vineet Gupta,
Anna Greka,
George W. Burke,
Peter Mündel
Publication year - 2013
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1304572
Subject(s) - abatacept , medicine , proteinuria , focal segmental glomerulosclerosis , kidney transplantation , nephrotic syndrome , immunology , transplantation , rituximab , urology , kidney , antibody
Abatacept (cytotoxic T-lymphocyte-associated antigen 4-immunoglobulin fusion protein [CTLA-4-Ig]) is a costimulatory inhibitor that targets B7-1 (CD80). The present report describes five patients who had focal segmental glomerulosclerosis (FSGS) (four with recurrent FSGS after transplantation and one with primary FSGS) and proteinuria with B7-1 immunostaining of podocytes in kidney-biopsy specimens. Abatacept induced partial or complete remissions of proteinuria in these patients, suggesting that B7-1 may be a useful biomarker for the treatment of some glomerulopathies. Our data indicate that abatacept may stabilize β1-integrin activation in podocytes and reduce proteinuria in patients with B7-1-positive glomerular disease.
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