Plasma cell biology: Foundations for targeted therapeutic development in transplantation.
Amy P RossiRaymond T ChungDavid A HildemanErvin Steve WoodlePublished in: Immunological reviews (2021)
Solid organ transplantation is a life-saving procedure for patients with end-stage organ disease. Over the past 70 years, tremendous progress has been made in solid organ transplantation, particularly in T-cell-targeted immunosuppression and organ allocation systems. However, humoral alloimmune responses remain a major challenge to progress. Patients with preexisting antibodies to human leukocyte antigen (HLA) are at significant disadvantages in regard to receiving a well-matched organ, moreover, those who develop anti-HLA antibodies after transplantation face a significant foreshortening of renal allograft survival. Historical therapies to desensitize patients prior to transplantation or to treat posttransplant AMR have had limited effectiveness, likely because they do not significantly reduce antibody levels, as plasma cells, the source of antibody production, remain largely unaffected. Herein, we will discuss the significance of plasma cells in transplantation, aspects of their biology as potential therapeutic targets, clinical challenges in developing strategies to target plasma cells in transplantation, and lastly, novel approaches that have potential to advance the field.
Keyphrases
- induced apoptosis
- cell therapy
- randomized controlled trial
- endothelial cells
- end stage renal disease
- oxidative stress
- ejection fraction
- immune response
- stem cells
- newly diagnosed
- endoplasmic reticulum stress
- cancer therapy
- minimally invasive
- risk assessment
- climate change
- cell proliferation
- prognostic factors
- mesenchymal stem cells
- drug delivery
- peritoneal dialysis
- patient reported