Evidence map›Paper›PMID 31219185›Full record

Trial reportBritish journal of haematology2019

T-cell receptor sequencing demonstrates persistence of virus-specific T cells after antiviral immunotherapy.

Michael D Keller, Sam Darko, Haili Lang, Amy Ransier, Christopher A Lazarski, Yunfei Wang, Patrick J Hanley, Blachy J Davila, Jennifer R Heimall, Richard F Ambinder and 5 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in British journal of haematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 1 country.

Michael D KellerDivision of Allergy & Immunology, Children's National Health System, Washington, DC, USA.ORCID 0000-0001-8323-3085
Sam DarkoVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD, USA.
Haili LangCenter for Cancer and Immunology Research, Children's National Health System, Washington, DC, USA.
Amy RansierVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD, USA.
Christopher A LazarskiCenter for Cancer and Immunology Research, Children's National Health System, Washington, DC, USA.
Yunfei WangClinical and Translational Sciences Institute, Children's National Health System, Washington, DC, USA.
Patrick J HanleyCenter for Cancer and Immunology Research, Children's National Health System, Washington, DC, USA.
Blachy J DavilaDivision of Blood and Marrow Transplantation, Children's National Health System, Washington, DC, USA.
Jennifer R HeimallDivision of Allergy & Immunology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Richard F AmbinderDivision of Blood and Marrow Transplantation, Johns Hopkins Hospital, Baltimore, MD, USA.ORCID 0000-0003-4027-3073
A John BarrettGW Cancer Center, George Washington University, Washington, DC, USA.
Cliona M RooneyCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston Methodist Hospital and Texas Children's Hospital, Houston, TX, USA.
Helen E HeslopCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston Methodist Hospital and Texas Children's Hospital, Houston, TX, USA.
Daniel C DouekVaccine Research Center, National Institute of Allergy and Infectious Disease, Bethesda, MD, USA.
Catherine M BollardCenter for Cancer and Immunology Research, Children's National Health System, Washington, DC, USA.
Children's National · USNational Institute of Allergy and Infectious Diseases · USHouston Methodist · USChildren's Hospital of Philadelphia · USGeorge Washington University · USJohns Hopkins Hospital · US

Funding

Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Leonid S Metelitsa · 2007 to 2026
$51.4M
PR1-specific CB T cells for Patients with Myeloid MalignanciesP01CA148600 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BOLLARD, CATHERINE M., SHPALL, ELIZABETH J · 2011 to 2022
$24.4M
The Genome Analysis CoreZICAI005133 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DOUEK, DANIEL CESAR · 2019 to 2025
$16.9M
T Cell Immune Responses To HIV And Other PathogensZIAAI005033 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DOUEK, DANIEL CESAR · 2009 to 2025
$11.4M
Anti-viral and antileukemic T-cell therapy as prophylaxis after HSCTU10HL108945 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI HESLOP, HELEN E · 2011 to 2016
$954k
Adoptive Immunotherapy for the Treatment of Viral Infections in Primary Immunodeficiency DisordersK23HL136783 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI KELLER, MICHAEL DANIEL · 2017 to 2019
$614k
NCI NIH HHS P01 CA148600NCI NIH HHS P50 CA126752NHLBI NIH HHS K23 HL136783NHLBI NIH HHS U10 HL108945
6 · The paper itself

Abstract

Viral infections are a serious cause of morbidity and mortality following haematopoietic stem cell transplantation (HSCT). Adoptive cellular therapy with virus-specific T cells (VSTs) has been successful in preventing or treating targeted viruses in prior studies, but the composition of ex vivo expanded VST and the critical cell populations that mediate antiviral activity in vivo are not well defined. We utilized deep sequencing of the T-cell receptor beta chain (TCRB) in order to classify and track VST populations in 12 patients who received VSTs following HSCT to prevent or treat viral infections. TCRB sequencing was performed on sorted VST products and patient peripheral blood mononuclear cells samples. TCRB diversity was gauged using the Shannon entropy index, and repertoire similarity determined using the Morisita-Horn index. Similarity indices reflected an early change in TCRB diversity in eight patients, and TCRB clonotypes corresponding to targeted viral epitopes expanded in eight patients. TCRB repertoire diversity increased in nine patients, and correlated with cytomegalovirus (CMV) viral load following VST infusion (P = 0·0071). These findings demonstrate that allogeneic VSTs can be tracked via TCRB sequencing, and suggests that T-cell receptor repertoire diversity may be critical for the control of CMV reactivation after HSCT.

Indexed as

CytomegalovirusImmunotherapy, AdoptiveCytomegalovirus InfectionsFemaleHematopoietic Stem Cell TransplantationHumansMaleReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesViral LoadReceptors, Antigen, T-Cell, alpha-betaadoptive immunotherapyhaematopoietic stem cell transplantationT-lymphocyteviral infection

Identifiers

PMID31219185
PMCPMC6786907
OpenAlexW2951576316

What OpenQuestion holds

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Registered trials

None linked

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.