ATC Abstracts

American Transplant Congress abstracts

  • Home
  • Meetings Archive
    • 2020 American Transplant Congress
    • 2019 American Transplant Congress
    • 2018 American Transplant Congress
    • 2017 American Transplant Congress
    • 2016 American Transplant Congress
    • 2015 American Transplant Congress
    • 2013 American Transplant Congress
  • Keyword Index
  • Resources
    • 2016 Resources
      • 2016 Welcome Letter
      • ATC 2016 Program Planning Committees
      • ASTS Council 2015-2016
      • AST Board of Directors 2015-2016
    • 2015 Resources
      • 2015 Welcome Letter
      • ATC 2015 Program Planning Committees
      • ASTS Council 2014-2015
      • AST Board of Directors 2014-2015
      • 2015 Conference Schedule
  • Advanced Search

Polyclonal Treg Adoptive Therapy for Control of Subclinical Kidney Transplant Inflammation (TASK Pilot Trial).

S. Chandran, Q. Tang, M. Sarwal, Z. Laszik, A. Putnam, T. Sigdel, E. Tavares, J. Bluestone, F. Vincenti.

UCSF, San Francisco, CA.

Meeting: 2016 American Transplant Congress

Abstract number: 412

Keywords: Inflammation, Kidney transplantation, Polyclonal, T cells

Session Information

Date: Tuesday, June 14, 2016

Session Name: Concurrent Session: Kidney Immunosuppression: Novel Agents

Session Time: 2:30pm-4:00pm

 Presentation Time: 2:30pm-2:42pm

Location: Veterans Auditorium

Related Abstracts
  • Results of a Phase 1 Trial of Treg Adoptive Cell Transfer (TRACT) in De Novo Living Donor Kidney Transplant Recipients.
  • Interim Results of a Phase 1 Trial of Treg Adoptive Cell Transfer (TRACT) in Living Donor Kidney Transplant Recipients

Purpose: Early renal graft inflammation is associated with progressive fibrosis & late dysfunction. Treg therapy can reverse established inflammation in animal models. We conducted a pilot safety & feasibility trial of Treg therapy for subclinical kidney transplant inflammation.

Methods: Peripheral blood CD4+CD25+CD127lo/- Tregs were isolated using FACS & expanded ex vivo for 2 wks with anti-CD3/anti-CD28 stimulations/IL-2 in a deuterated glucose-containing medium to label Tregs. Stable kidney transplant recipients with subclinical inflammation on 6-mth protocol biopsies received a single infusion of 320×106 Tregs. %Deuterium enrichment by GC-MS allowed estimation of levels of infused (labeled) Tregs in circulation. Inflammation was assessed on kidney biopsies using Banff scoring and leukocyte common antigen positive (LCA+) cell density & in urine using common rejection module (uCRM), an 11-gene biomarker of acute rejection.

Results: Two kidney transplant recipients on tac/MMF/prednisone received Treg infusions and 6 mths of follow-up. Tregs expanded >100-fold and met all release criteria for infusion. Infused Tregs peaked within wk 1, representing up to 7.5% of all circulating Tregs (Figure). Decay of infused Tregs was similar to that noted in non-immunosuppressed patients treated with the same dose. Graft inflammation improved in both patients (Table). uCRM data are being analyzed. One patient had transient lymphopenia (day 4-21) post-infusion. No infusion reactions, infections or acute rejections were seen & graft function remained stable.

Conclusions: It is feasible to isolate & expand Tregs from transplanted patients on immunosuppression. Infused Tregs were well tolerated & had pharmacokinetics similar to those in non-immunosuppressed patients. CTOT-21 will test the efficacy of polyclonal and alloreactive Tregs for control of subclinical graft inflammation.

Subject Kidney Biopsy Time Banff Score LCA+ Cells/mm2
TASKp1 Baseline i1 t1 337.2
  2 weeks i0 t0 18.9
  6 months i0 t0  126.1
TASKp2 Baseline i0 t1 469.1
  2 weeks i0 t0 303.5
  6 months i0 t1 74.9

CITATION INFORMATION: Chandran S, Tang Q, Sarwal M, Laszik Z, Putnam A, Sigdel T, Tavares E, Bluestone J, Vincenti F. Polyclonal Treg Adoptive Therapy for Control of Subclinical Kidney Transplant Inflammation (TASK Pilot Trial). Am J Transplant. 2016;16 (suppl 3).

  • Tweet
  • Email
  • Print

To cite this abstract in AMA style:

Chandran S, Tang Q, Sarwal M, Laszik Z, Putnam A, Sigdel T, Tavares E, Bluestone J, Vincenti F. Polyclonal Treg Adoptive Therapy for Control of Subclinical Kidney Transplant Inflammation (TASK Pilot Trial). [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/polyclonal-treg-adoptive-therapy-for-control-of-subclinical-kidney-transplant-inflammation-task-pilot-trial/. Accessed April 20, 2021.

« Back to 2016 American Transplant Congress

Most Viewed Abstracts

  • This Week
  • This Month
  • All Time
  • Subtherapeutic Low Tacrolimus Trough Levels (≤3.5 Ng /ml) Are A Risk Factor For Acute Rejection And Creatinine Doubling.
  • Low GFR after Kidney Donation Is Not Chronic Kidney Disease
  • Is There a Difference Between DCD and DBD Kidney Transplantation with Similar KDPI?
  • Penis Transplantation: First U.S. Experience.
  • Live Related Kidney Transplant Experience in Abuja, Nigeria – First Eight Cases Ever.
    • Assessment of Anti-A and Anti-B Antibody Titers in Different IVIG Preparations: Correlation with Risk for Hemolysis

    Visit Our Partner Sites

    American Transplant Congress (ATC)

    Visit the official site for the American Transplant Congress »

    American Journal of Transplantation

    The official publication for the American Society of Transplantation (AST) and the American Society of Transplant Surgeons (ASTS) »

    American Society of Transplantation (AST)

    An organization of more than 3000 professionals dedicated to advancing the field of transplantation. »

    American Society of Transplant Surgeons (ASTS)

    The society represents approximately 1,800 professionals dedicated to excellence in transplantation surgery. »

    Copyright © 2013-2021 by American Society of Transplantation and the American Society of Transplant Surgeons. All rights reserved.

    Privacy Policy | Terms of Use

    loading Cancel
    Post was not sent - check your email addresses!
    Email check failed, please try again
    Sorry, your blog cannot share posts by email.
    This site uses cookies: Find out more.