Paired Marrow Aspirations to Assess Assays in Sensitized Renal Allograft Recipients

NCT ID: NCT01150487

Last Updated: 2025-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

288 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-10-05

Study Completion Date

2025-12-15

Brief Summary

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The aim of this study is to determine a comprehensive immune profile of transplant donors and recipients through assessment of immune cell compositions in bone marrow, and lymph nodes.

Detailed Description

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The aim of this risk protocol is to determine the variability of the AlloElispot and Allospecificities assay.

Our group has developed a number of assays to assess the immune cell population in our transplant population. This has included: 1) the number of donor-specific alloantibody (DSA) secreting bone marrow derived plasma cells (AlloELISPOT assay), 2) the function of DSA-secreting Plasma cells (Allospecificities assay), 3)Culture of plasma cells in human stromal cells to produce specific HLA antibodies and tetanus antibodies, 4) Understand the critical pathways for the survival and function of plasma cells, 5)Characterize the different phenotypes and genotypes of the plasma cell, 6)Phenotype analyses of the immune cell population using flow cytometry and/or mass spectrometry (ie. cytometry by time of flight/CyTOF), 7)Functional assessments of T and B-cells, and 8)T-cell receptor diversity.

These assays were developed over the years and already have provided an important means of testing new therapeutic protocols aimed at controlling DSA production. It is important to note that repeated attempts to isolate PCs from peripheral blood have been unsuccessful (PCs are extremely rare in peripheral blood) and the bone marrow is the only accessible source of PCs.

It is now clear to that we have reached a point that we must validate these assays (coefficient of variation, etc), in order to appropriately evaluate data derived from these assays. Inter-assay variability can be assessed by performing two paired assays in the same patient. This could be done in two ways-paired bone marrow aspirations separated by time or two bone marrow aspirations performed at the same time. We have decided to pursue the latter approach. We will do both marrows either at the time of transplantation or while they are undergoing a surgical procedure. Lymph node retrieval will also be performed at the time for abstraction of immune cells for additional analysis. We believe that this is safe and will be well-tolerated and will provide the data that we need to validate the assays.

Conditions

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Transplantation, Kidney Living Donors Kidney Transplant Recipients

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Kidney recipients or kidney donors

Patients who have had a Kidney transplant or are undergoing a kidney transplant. Kidney donors.

Group Type EXPERIMENTAL

bone marrow aspirations

Intervention Type PROCEDURE

A bone marrow aspiration from each hip bone of the patients.

lymph node collection

Intervention Type PROCEDURE

An Iliac lymph node collection.

Interventions

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bone marrow aspirations

A bone marrow aspiration from each hip bone of the patients.

Intervention Type PROCEDURE

lymph node collection

An Iliac lymph node collection.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Pre or post renal transplant recipients.
* Renal transplant donors.
* Those who give voluntary written informed consent before performance of any study-related procedures, which are not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.

Exclusion Criteria

* Any patient currently receiving systemic anticoagulation therapy with heparin or coumadin.
* Patient has a platelet count of \<30 x 10(9)/L within 14 days before enrollment.
* Patient has an absolute neutrophil count of ANC\<1.0 x 10(9)/L within 14 days before enrollment.
* Patient has received other investigational drugs within14 days before enrollment.
* Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
* Diagnosed or treated for malignancy within 5 years of enrollment, with the exception of complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, or low-risk prostate cancer after curative therapy.
* Contraindication to kidney transplantation or donation-active infection, comorbid medical conditions, etc
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role collaborator

Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Mark Stegall

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mark Stegall, MD

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

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Mayo Clinic

Rochester, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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R21AI125719

Identifier Type: NIH

Identifier Source: secondary_id

View Link

10-002572

Identifier Type: -

Identifier Source: org_study_id