Drug intelligence / Profile preview

IVIG + rituximab

Development stage
Unknown
Lead developer
Cedars-Sinai
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

This desensitization protocol, developed at Cedars-Sinai Medical Center, combines intravenous immunoglobulin (IVIG) and rituximab to manage highly HLA-sensitized patients awaiting kidney transplantation. Rituximab is a chimeric monoclonal antibody targeting the CD20 antigen on B cells, leading to their depletion and a reduction in the production of new anti-HLA antibodies. IVIG, a pooled human plasma product, provides immediate immunomodulation by neutralizing circulating antibodies, inhibiting complement-mediated injury, and modulating Fc receptor signaling. Together, these agents lower the levels of donor-specific antibodies (DSAs), enabling successful transplantation in patients who would otherwise face high risks of hyperacute or antibody-mediated rejection.

Other names
IVIG + rituximab-Cedars-Sinai Medical Center-kidney transplantationCedars-Sinai desensitization protocolJordan protocolIVIG and Rituximab for Desensitization
02

Targets

CD20 (B-lymphocyte antigen CD20)FcγRIIIa (Low affinity immunoglobulin gamma Fc region receptor III-A)FcγR (Low affinity immunoglobulin gamma Fc region receptor II-c)C1Q (Complement C1q)

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