Evidence map›Paper›PMID 40609742›Full record

ArticleTransplantation and cellular therapy2025

Understanding Telomere Biology in Hematopoietic Cell Transplantation: A Dynamical Systems Perspective.

Amir A Toor, Morgan Horton, Haniya Khalid, Elizabeth Krieger, Tsung-Po Lai, Stephen R Spellman, John E Levine, Wael Saber, Valerie Stewart, Shahinaz M Gadalla

Abstract read
In one paragraph

Article in Transplantation and cellular therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Amir A ToorHarold C. Simmons Cancer Center, University of Texas Southwestern, Dallas, Texas. Electronic address: amir.toor@utsouthwestern.edu.
Morgan HortonLehigh Valley Health Network, Allentown, Pennsylvania.
Haniya KhalidLehigh Valley Health Network, Allentown, Pennsylvania.
Elizabeth KriegerChildren's Hospital of Richmond at Virginia Commonwealth University, Richmond, Virginia.
Tsung-Po LaiCenter of Human Development and Aging, New Jersey Medical School, Rutgers, New Jersey.
Stephen R SpellmanCenter for International Blood and Marrow Transplant Research, NMDP, Minneapolis, Minnesota.
John E LevineTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Wael SaberCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Valerie StewartCenter for International Blood and Marrow Transplant Research, NMDP, Minneapolis, Minnesota.
Shahinaz M GadallaDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland. Electronic address: gadallas@nih.gov.

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Blood and Marrow Transplant Clinical Trials Network DCC- The Medical College of Wisconsin, Inc.U24HL138660 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Steven M. DeVine, Mehdi Hussain Hamadani · 2017 to 2026
$71.4M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
Institutional Career Development CoreKL2TR003018 · NCATS · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI CHAN, JOHN R., HALM, ETHAN A · 2019 to 2023
$3.0M
Telomere Length Measurements: Strengths and LimitationsU01AG066529 · NIA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI AVIV, ABRAHAM · 2019 to 2021
$911k
Intramural NIH HHS Z99 CA999999NCATS NIH HHS KL2 TR003018NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294NHLBI NIH HHS U24 HL138660NIA NIH HHS U01 AG066529
6 · The paper itself

Abstract

backgroundT cell proliferation and repertoire reconstitution is a hallmark of successful hematopoietic cell transplantation (HCT). This process may be modeled as a dynamical system and in such a system, precise telomere length (TL) measurement may reflect the proliferative capacity of donor T cells. TL for different chromosomes span a few orders of magnitude, and different blood cell populations including T cell clones display variable TL; these differences across the cell populations are not represented when examining average leukocyte TL. This study aims to develop a method that integrates the entire spectrum of TL observed within a sample to better understand the influence on clinical outcomes following HCT.

methodsTo better reflect the entire span of TL, we used data generated using the Telomere Shortest Length Assay (TeLSA) that provides discrete measurements of individual telomeres for each blood DNA sample. TeSLA leukocyte TL (LTL) measurements were performed on 72 paired samples collected from the donor pretransplant (D-LTL) and the recipient 90 days following HCT (post-HCT LTL). Area under the curve (AUC) calculations were used to incorporate the full distribution of measured LTL from each sample. The magnitude of LTL shortening after HCT was calculated as the difference between the AUCs for D-LTL and corresponding post-HCT LTL, and referred to as AUC delta-TL.

resultsTelomere band lengths ranged from 350 base pairs to 16.7 kilobases with a logarithmically declining distribution in all samples when arrayed in descending order. The AUC delta-TL predicted patient overall survival (OS; P-log rank <.0001); HCT recipients with an intermediate degree of TL shortening (25

conclusionThe findings described herein suggest that the degree of donor telomere attrition may correlates with clinical outcomes following transplant, possibly reflecting alloreactive T cell expansion. Accounting for the entire span of telomere lengths, may better identify post-transplant risk groups.

Indexed as

Hematopoietic Stem Cell TransplantationTelomereAdolescentAdultFemaleHumansMaleMiddle AgedYoung AdultArea under the curveHematopoietic cell transplantationTelomeres

Identifiers

PMID40609742
PMCPMC12415981

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.