Deep Phenotyping of the Renal Allograft to Prognosticate Clinical Outcomes

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Pittsburgh

About this trial

The goal of this observational study is to determine phenotypic, transcriptional, and epigenetic underpinnings of renal allograft rejection in renal transplant rejection. The main questions it aims to answer are:

* To determine the phenotype, frequency, location, and the inter-cellular interactions between the cells that constitute intra-graft inflammatory infiltrate in acute ejection. * To determine the phenotype, frequency, location, and the inter-cellular interactions between the cells that constitute intra-graft inflammatory infiltrate in recurrent/recalcitrant rejection vs. rejection that resolves with therapy. * To generate a scRNA sequencing (scRNAseq) map of the intra-graft immune cells and the renal parenchymal cells and compare the transcriptional and epigenetic changes within these cells in recurrent/recalcitrant rejection vs. rejection that resolves with therapy. * To determine phenotypic changes associated with chronic rejection.

Participants will be asked to provide the following research specimens:

* Renal biopsy specimens at the following timepoints: day of transplantation (pre-implantation and post-perfusion); routine protocol biopsies at 3 months and 12 months; and clinically indicated for-cause biopsies at any timepoint from time-0 to 1-yr post-transplantation. The 1st research core will be used for routine histopathological examination and left over tissue from this core will be used for deep phenotyping using multiparameter immunophenotyping, and digital spatial profiling. The second research core will be used for extraction of cells and nuclei for scRNAseq and snATACseq. * Blood samples will be processed to obtain plasma (for cytokine, chemokine and DSA measurements) and PBMC (for deep phenotyping and molecular analyses). For each collection timepoint, up to 75 mL (about 5 tablespoons) will be collected. * Prospective clinical data and outcomes will be collected from participant medical records. * Follow-Up Period: For-cause biopsies from 1-yr to 5-yr post-transplantation (by the transplant nephrologist): no additional cores will be obtained for research from these biopsies. The left-over tissue from the clinically indicated biopsy cores will be analyzed by deep phenotyping and digital spatial profiling. Blood samples will be processed to obtain plasma (for cytokine, chemokine and DSA measurements) and PBMC (for deep phenotyping and molecular analyses).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All adult living or deceased donor renal transplant recipients (age ≥ 18 years), irrespective of gender, race, or ethnic background.

Able to understand and provide inform consent.

Disqualifiers

Medical contraindications to undergo renal biopsy (use of long-term anticoagulation, low platelet count of <100,000/uL)

Cause of ESRD likely to recur in transplant: Hemolytic uremic syndrome (HUS)

Not maintained on standard of care immunosuppression therapy (Thymoglobulin induction followed by tacrolimus and mycophenolate maintenance)

Trial population

Adult living donor or deceased donor renal transplant recipients

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

24 Participants
are grouped into 1 trial group
Group A: Renal transplantation recipients

Trial outcomes

Primary outcomes

1

Percentage of Participants with Biopsy Proven Acute Rejection at one year

Percentage biopsy proven acute rejection either on a surveillance biopsy or a for-cause biopsy in the First Post-Transplant Year

Time frame
1 year
2

Degree of Correlation of Acute Rejection Transcriptional Changes Within the Infiltrating Inflammatory Cells at one year

Degree of Correlation of Transcriptional Changes Within the Infiltrating Inflammatory Cells Assessed by scRNA Sequencing in the First Post-Transplant Year

Time frame
1 year
3

Percentage of Correlation of Transcriptional Changes Within the Renal Parenchymal Cells at one year

Percentage Correlation of Acute Rejection Transcriptional Changes Within the Renal Parenchymal Cells Assessed by scRNA Sequencing in the First Post-Transplant Year

Time frame
1 year

Secondary outcomes

1

Percentage of Histological Persistence of Rejection at one year

Percentage Histological Persistence of Rejection in the First Post-Transplant Year

Time frame
1 year
2

Degree of Correlation of Histological Transcriptional Changes Within the Infiltrating Inflammatory Cells at one year

Degree of Correlation of Histological Transcriptional Changes Within the Infiltrating Inflammatory Cells in the First Post-Transplant Year

Time frame
1 Year
3

Degree of Correlation of Histological Transcriptional Changes Within the Renal Parenchymal Cells at one year

Degree of Correlation of Histological Transcriptional Changes Within the Renal Parenchymal Cells in the First Post-Transplant Year

Time frame
1 Year
4

Percentage of Participants with Biopsy Proven Acute Rejection at Year 3

Percentage biopsy proven acute rejection either on a surveillance biopsy or a for-cause biopsy in the Third Post-Transplant Year

Time frame
3 Years

Other outcomes

Sponsors and contacts

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