Abstract

The presence of anti-human leucocyte antigen (HLA) antibodies in the potential solid organ transplant recipient’s blood is one of the main barriers to access to a transplantation. The HLA sensitization is associated with longer waitlist time, antibody mediated rejection and transplant lost leading to increased recipient’s morbidity and mortality. However, solid organ transplantation across the HLA immunological barriers have been reported in recipients who were highly sensitized to HLA using desensitization protocols. These desensitization regimens are focused on the reduction of circulating HLA antibodies. Despite those strategies improve rates of transplantation, it remains several limitations including persistent high rejection rate and worse long-term outcomes when compare with non-sensitized recipient population. Currently, interest is growing in the development of new desensitization approaches which, beyond targeting antibodies, would be based on the modulation of alloimmune pathways. Plasma cells appears as an interesting target given their critical role in antibody production. In the last decade, CD38-targeting immunotherapies, such as daratumumab, have been recognized as a key component in the treatment of myeloma by inducing an important plasma cell depletion. This review focuses on an emerging concept based on targeting CD38 to desensitize in the field of transplantation.

Highlights

  • human leucocyte antigens (HLA) Sensitization and Antibody-Mediated RejectionSolid organ transplantation (SOT) has become the best therapeutic option for end-stage organ disease but faces two major issues: the limited transplant supply and the poor long-term transplants outcome which have not improved over the past 30 years [1,2,3]

  • We propose to focus on anti-CD38 as a desensitization regimen in Sensitization and Antibody-Mediated RejectionSolid organ transplantation (SOT)

  • Therapeutic improvement is required for both prevention and treatment of humoral alloresponse in solid organ transplantation

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Summary

INTRODUCTION

Solid organ transplantation (SOT) has become the best therapeutic option for end-stage organ disease but faces two major issues: the limited transplant supply and the poor long-term transplants outcome which have not improved over the past 30 years [1,2,3] This observation is related to the occurrence of antibody-mediated rejection (ABMR) which remains the death-censored leading cause of transplant loss across all solid organ transplants [3, 4]. On the other hand, keeping patients a long time on dialysis represent a considerable financial burden while decreasing the quality and length of life for affected patients [32, 33].it appear as necessary to develop novel therapeutic approaches in order to prevent ABMR and improve long-term survival of transplanted organs in highly immunized recipient

Desensitization Regimens Targeting Plasma Cells
NCT number
Immune event
Significant reduction of DSA levels and prolonged graft survival
Findings
CONCLUSION
Full Text
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