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Prompt reversal of a severe complement activation by eculizumab in a patient undergoing intentional ABO‐incompatible pancreas and kidney transplantation

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TLDR
This potentially first intentional ABO‐incompatible deceased‐donor kidney and pancreas transplantation with a severe antibody‐mediated rejection during a rebound of isoagglutinins suggests that ABO barriers can be overcome without extensive preconditioning, when the complement inhibitor eculizumab is included.
Abstract
We describe the presumably first intentional ABO-incompatible deceased-donor kidney and pancreas transplantation with a severe antibody-mediated rejection during a rebound of isoagglutinins Rejection was successfully treated with eculizumab, which inhibits the terminal pathway of complement Complement analysis (C3, C3d,g, and a modified assay of classical complement-related hemolytic function) documented complement activation and confirmed that eculizumab completely blocked complement function At 6 months, the patient had normal kidney and pancreas function, and histological evaluations revealed no evidence of sustained graft damage This successful transplantation suggests that ABO barriers can safely be overcome without extensive preconditioning, when the complement inhibitor eculizumab is included

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Journal ArticleDOI

Compstatin: a C3-targeted complement inhibitor reaching its prime for bedside intervention

TL;DR: An up‐to‐date survey of the drug design effort placed on the compstatin family of C3 inhibitors, highlighting the most promising drug candidates and discusses translational challenges in complement drug discovery and peptide drug development.
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ABO-Incompatible Kidney Transplantation.

TL;DR: There is still concern, however, that infectious complications such as viral disease, Pneumocystis jirovecii pneumonia, and severe urinary tract infections are increased after ABOi transplantations.
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C1 Inhibitor in Acute Antibody-Mediated Rejection Nonresponsive to Conventional Therapy in Kidney Transplant Recipients: A Pilot Study.

TL;DR: C1‐INH added to IVIG is safe and may improve allograft function in kidney recipients with nonresponsive acute ABMR that is nonresponsive to conventional therapy.
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Infections associated with the use of eculizumab: recommendations for prevention and prophylaxis.

TL;DR: Eculizumab has opened new horizons in the treatment of complement-mediated disorders and is expanding beyond complement- mediated diseases to transplantation and neurology, and prevention strategies against the risk of Neisseria spp.
References
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Journal ArticleDOI

Reshaping human antibodies for therapy.

TL;DR: A human IgGI antibody has been reshaped for serotherapy in humans by introducing the six hypervariable regions from the heavy- and light-chain variable domains of a rat antibody directed against human lymphocytes.
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Inhibition of complement activity by humanized anti-C5 antibody and single-chain Fv

TL;DR: These results demonstrate that humanized h5G1.1 and its recombinant derivatives retain both the affinity and blocking functions of the murine 5G 1.1 antibody, and suggest that these molecules may serve as potent inhibitors of complement-mediated pathology in human inflammatory diseases.
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Implementation of a Protocol for ABO-incompatible kidney transplantation--a three-center experience with 60 consecutive transplantations.

TL;DR: A significant inter-institutional variation in the measurement of anti-AB-antibodies was found, having a substantial impact on the number of immunoadsorptions and consequently on the total cost for the procedure.
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Pancreas transplantation in the United States: a review.

TL;DR: With modern immunosuppressive protocols and careful donor selection, patient survival rates and pancreas transplant graft function can be further improved in all three pancrea transplant categories.
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Generation of iC3 at the interface between blood and gas.

TL;DR: The rate of iC3/iC3 fragments generation was unaffected by the composition of the gas (pure oxygen, pure nitrogen or air), suggesting that the denaturation of C3 indeed occurred at the serum gas interface.
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