Phase 3 Clinical Candidate Rilparencel Demonstrates Weak Association with Renal Epithelial Senescence-Associated Secretory Phenotype

Background: CKD is associated with an enhanced senescence-associated secretory phenotype (SASP) and high inflammation, which can induce senescence. This study evaluated the renal epithelial SASP of rilparencel. Biopsy-derived rilparencel is a first-in-class autologous renal epithelial cell product in Phase 3 clinical trials for patients with T2D and CKD. Data from two Phase 2 clinical trials suggest that cortical administration of rilparencel potentially stabilizes estimated glomerular filtration rate (eGFR). Methods: rilparencel manufactured from kidney biopsies of each of 5 patients with T2D and CKD (NCT02836574) was submitted for scRNA-seq, and 52 differentially expressed genes (DEGs) were evaluated for this study. Additionally, for each patient, proteins secreted by rilparencel were compared to proteins secreted from a manufacturing precursor to rilparencel (Intelliflex). Fifty-one secreted proteins and 52 DEGs were seeded into the SASP atlas, a proteomic analysis of renal epithelial cells 10 days post-irradiation (PMID:31945054), to determine if any are associated with a renal epithelial SASP. As comparison, IGFBP2 and CXCL8, senescence markers known to be elevated in CKD, were used as positive controls. Results: Of the secreted proteins and DEGs associated with rilparencel, only PTER (a DEG) was identified as being secreted by renal epithelial cells according to the SASP atlas. The SASP atlas reports that PTER protein expression is approximately 2-fold less than IGFBP2 and CXCL8, which serve as positive SASP controls for comparison (A). Additionally, rilparencel secretes reduced levels of proinflammatory cytokines compared to an earlier stage in the product manufacture (B), which also suggests a reduced senescence phenotype. Conclusion: Our proprietary manufacturing process generates a renal epithelial cell-based product (rilparencel) from renal cortex tissue with a low SASP, which may in part underlie its therapeutic activity in the clinic. Funding: Commercial Support - ProKidney LLC

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Publication Details

Journal
Journal of the American Society of Nephrology
Published
2024-10-01
DOI
https://doi.org/10.1681/asn.2024g1z2sw1e
Primary Topic
Biomedical Ethics and Regulation
Type
article
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article

Phase 3 Clinical Candidate Rilparencel Demonstrates Weak Association with Renal Epithelial Senescence-Associated Secretory Phenotype

Dominic Mark Justewicz, Mark A. Rohlfing, Björn Bauer, Andrew T. Bruce et al.
Journal of the American Society of Nephrology
Biomedical Ethics and Regulation
article

Phase 3 Clinical Candidate Rilparencel Demonstrates Weak Association with Renal Epithelial Senescence-Associated Secretory Phenotype

Dominic Mark Justewicz, Mark A. Rohlfing, Björn Bauer, Andrew T. Bruce, Ashley Greenawalt
article en

Abstract

Background: CKD is associated with an enhanced senescence-associated secretory phenotype (SASP) and high inflammation, which can induce senescence. This study evaluated the renal epithelial SASP of rilparencel. Biopsy-derived rilparencel is a first-in-class autologous renal epithelial cell product in Phase 3 clinical trials for patients with T2D and CKD. Data from two Phase 2 clinical trials suggest that cortical administration of rilparencel potentially stabilizes estimated glomerular filtration rate (eGFR). Methods: rilparencel manufactured from kidney biopsies of each of 5 patients with T2D and CKD (NCT02836574) was submitted for scRNA-seq, and 52 differentially expressed genes (DEGs) were evaluated for this study. Additionally, for each patient, proteins secreted by rilparencel were compared to proteins secreted from a manufacturing precursor to rilparencel (Intelliflex). Fifty-one secreted proteins and 52 DEGs were seeded into the SASP atlas, a proteomic analysis of renal epithelial cells 10 days post-irradiation (PMID:31945054), to determine if any are associated with a renal epithelial SASP. As comparison, IGFBP2 and CXCL8, senescence markers known to be elevated in CKD, were used as positive controls. Results: Of the secreted proteins and DEGs associated with rilparencel, only PTER (a DEG) was identified as being secreted by renal epithelial cells according to the SASP atlas. The SASP atlas reports that PTER protein expression is approximately 2-fold less than IGFBP2 and CXCL8, which serve as positive SASP controls for comparison (A). Additionally, rilparencel secretes reduced levels of proinflammatory cytokines compared to an earlier stage in the product manufacture (B), which also suggests a reduced senescence phenotype. Conclusion: Our proprietary manufacturing process generates a renal epithelial cell-based product (rilparencel) from renal cortex tissue with a low SASP, which may in part underlie its therapeutic activity in the clinic. Funding: Commercial Support - ProKidney LLC

Journal of the American Society of NephrologyVol. 35(10S)
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Biomedical Ethics and Regulation
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Phase 3 Clinical Candidate Rilparencel Demonstrates Weak Association with Renal Epithelial Senescence-Associated Secretory Phenotype — Dominic Mark Justewicz, Mark A. Rohlfing, et al. · Journal of the American Society of Nephrology (2024) | TGRS Research Map | TGRS