Evidence map›Paper›PMID 26055301›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

Adaptive Natural Killer Cell and Killer Cell Immunoglobulin-Like Receptor-Expressing T Cell Responses are Induced by Cytomegalovirus and Are Associated with Protection against Cytomegalovirus Reactivation after Allogeneic Donor Hematopoietic Cell Transplantation.

Zachary B Davis, Sarah A Cooley, Frank Cichocki, Martin Felices, Rose Wangen, Xianghua Luo, Todd E DeFor, Yenan T Bryceson, Don J Diamond, Claudio Brunstein and 8 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

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  16. Low-Level Cytomegalovirus Antigenemia Promotes Protective Cytomegalovirus Antigen-Specific T Cells after Allogeneic Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2020
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Zachary B DavisBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Sarah A CooleyBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Frank CichockiBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Martin FelicesBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Rose WangenBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Xianghua LuoDivision of Biostatistics, School of Public Health and Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Todd E DeForBlood and Marrow Transplant Program, Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, Minnesota.
Yenan T BrycesonCentre for Infectious Medicine, Department of Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Don J DiamondDivision of Translational Vaccine Research, Beckman Research Institute of the City of Hope, Duarte, California.
Claudio BrunsteinBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
Bruce R BlazarBlood and Marrow Transplant Program, Department of Pediatric, University of Minnesota, Minneapolis, Minnesota.
John E WagnerBlood and Marrow Transplant Program, Department of Pediatric, University of Minnesota, Minneapolis, Minnesota.
Daniel J WeisdorfBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
Amir HorowitzStructural Biology and Microbiology and Immunology, Stanford University, Stanford, California.
Lisbeth A GuethleinStructural Biology and Microbiology and Immunology, Stanford University, Stanford, California.
Peter ParhamStructural Biology and Microbiology and Immunology, Stanford University, Stanford, California.
Michael R VernerisBlood and Marrow Transplant Program, Department of Pediatric, University of Minnesota, Minneapolis, Minnesota.
Jeffrey S MillerCentre for Infectious Medicine, Department of Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden. Electronic address: mille011@umn.edu.
University of Minnesota · USStanford University · USCity of Hope · USKarolinska University Hospital · SE

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, JEFFREY S. · 2005 to 2025
$38.2M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
TRAINING IN HEMOGLOBIN &CELL MEMBRANE RESEARCHT32HL007062 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller, Gregory M Vercellotti · 1985 to 2026
$10.3M
Viral priming and targeting NK cells against solid tumor malignanciesR35CA197292 · NCI · UNIVERSITY OF MINNESOTA · PI MILLER, JEFFREY S. · 2015 to 2021
$6.2M
Peptide Vaccine To Prevent CMV Disease After HSCTR01CA077544 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI DIAMOND, DON J · 1998 to 2017
$5.6M
GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
Evaluation of Protective CMV Vaccines in Rhesus MacaquesR01AI063356 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI BARRY, PETER A, DIAMOND, DON J · 2005 to 2014
$4.6M
HCMV Vaccine produced from BAC-MVA that Blocks Epithelial and Fibroblast EntryR01AI103960 · NIAID · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI BARRY, PETER A, DIAMOND, DON J · 2013 to 2016
$2.8M
Lymphoid Tissue Inducer/NK22 Cells and Post-transplant Immune RecoveryR01AI100879 · NIAID · UNIVERSITY OF MINNESOTA · PI VERNERIS, MICHAEL R. · 2013 to 2017
$1.9M
Inducing NK cells to remember and fight cancerR01HL122216 · NHLBI · UNIVERSITY OF MINNESOTA · PI MILLER, JEFFREY S. · 2015 to 2018
$1.5M
NCATS NIH HHS UL1 TR002494NCI NIH HHS CA65493NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS P30 CA077598NCI NIH HHS P30 CA 77598NCI NIH HHS R01 CA072669NCI NIH HHS R01 CA077544NCI NIH HHS R01 CA72669NCI NIH HHS R35 CA197292NHLBI NIH HHS R01 HL122216NHLBI NIH HHS T32 HL007062NIAID NIH HHS R01 AI063356NIAID NIH HHS R01 AI100879NIAID NIH HHS R01 AI103960NIAID NIH HHS R01 AI63356NICHD NIH HHS T32 HD007062
6 · The paper itself

Abstract

Cytomegalovirus (CMV) reactivates in >30% of CMV-seropositive patients after allogeneic hematopoietic cell transplantation (HCT). Previously, we reported an increase of natural killer (NK) cells expressing NKG2C, CD57, and inhibitory killer cell immunoglobulin-like receptors (KIRs) in response to CMV reactivation after HCT. These NK cells persist after the resolution of infection and display "adaptive" or memory properties. Despite these findings, the differential impact of persistent/inactive versus reactivated CMV on NK versus T cell maturation after HCT from different graft sources has not been defined. We compared the phenotype of NK and T cells from 292 recipients of allogeneic sibling (n = 118) or umbilical cord blood (UCB; n = 174) grafts based on recipient pretransplantation CMV serostatus and post-HCT CMV reactivation. This cohort was utilized to evaluate CMV-dependent increases in KIR-expressing NK cells exhibiting an adaptive phenotype (NKG2C(+)CD57(+)). Compared with CMV-seronegative recipients, those who reactivated CMV had the highest adaptive cell frequencies, whereas intermediate frequencies were observed in CMV-seropositive recipients harboring persistent/nonreplicating CMV. The same effect was observed in T cells and CD56(+) T cells. These adaptive lymphocyte subsets were increased in CMV-seropositive recipients of sibling but not UCB grafts and were correlated with lower rates of CMV reactivation (sibling 33% versus UCB 51%; P < .01). These data suggest that persistent/nonreplicating recipient CMV induces rapid production of adaptive NK and T cells from mature cells from sibling but not UCB grafts. These adaptive lymphocytes are associated with protection from CMV reactivation.

Indexed as

Cord Blood Stem Cell TransplantationHematopoietic Stem Cell TransplantationSiblingsAllograftsCytomegalovirusCytomegalovirus InfectionsFemaleHumansKiller Cells, NaturalMaleReceptors, KIRT-LymphocytesReceptors, KIRClinical outcomesCytomegalovirus reactivationNatural killer cellsTransplantation

Identifiers

PMID26055301
PMCPMC4557961
OpenAlexW1931293237

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Registered trials

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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.