Current progress in CAR-based therapy for kidney disease

Dan Zhang1, Dong Sun1,2,3

  • 1Department of Nephrology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

Frontiers in Immunology
|September 5, 2024
PubMed

Insights

Chimeric antigen receptor (CAR) T-cell therapy shows promise for treating immune-mediated kidney diseases. This approach engineers T cells to target and suppress autoimmune cells, offering new hope for refractory cases.

Area of Science:

  • Immunology
  • Nephrology
  • Cell Therapy

Background:

  • Immune-mediated kidney diseases present challenges due to poor treatment responses in some patients.
  • Existing therapies are insufficient for refractory renal disease cases.
  • Engineered T cells offer a novel therapeutic avenue for kidney diseases.

Purpose of the Study:

  • To review advancements in chimeric antigen receptor (CAR) T-cell therapies for immune-mediated kidney diseases.
  • To highlight the potential of CAR T-cell therapy in basic, translational, and clinical research.
  • To explore CAR T-cell applications in targeting autoreactive immune cells and alleviating autoimmune kidney conditions.

Main Methods:

  • Genetic modification of T cells to express chimeric antigen receptors (CARs).
  • Targeting autoreactive immune cells, including B cells and plasma cells.
  • Utilizing effector and regulatory T cells (Tregs) for autoimmune site-specific therapy.

Main Results:

  • CAR T-cell therapy enables precise targeting of autoimmune cells implicated in kidney disease.
  • Engineered T cells can migrate to sites of autoimmunity, proliferate, and exert suppressive functions.
  • This approach offers a novel strategy for alleviating autoimmune manifestations in the kidneys.

Conclusions:

  • CAR T-cell therapy represents a promising frontier for treating immune-mediated kidney diseases.
  • Genetically modified T cells provide a new mechanism to reduce autoinflammatory events.
  • Further research and clinical studies are warranted to fully realize the therapeutic potential of CAR T-cell interventions.

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