Evidence map›Paper›PMID 26416461›Full record

ArticleLeukemia2016

CD56dimCD57+NKG2C+ NK cell expansion is associated with reduced leukemia relapse after reduced intensity HCT.

F Cichocki, S Cooley, Z Davis, T E DeFor, H Schlums, B Zhang, C G Brunstein, B R Blazar, J Wagner, D J Diamond and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 205 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Reduced-Intensity Conditioning Followed by Related and Unrelated Allografts for Hematologic Malignancies: Expanded Analysis and Long-Term Follow-Up.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Cancer viroimmunotherapy platforms based on varicella-zoster virus and cytomegalovirus.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

F CichockiDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
S CooleyDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
Z DavisDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
T E DeForDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
H SchlumsCentre for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
B ZhangDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
C G BrunsteinDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
B R BlazarDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
J WagnerDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
D J DiamondDepartment of Experimental Therapeutics, Beckman Research Institute of City of Hope, Duarte, CA, USA.
M R VernerisLaboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
Y T BrycesonCentre for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
D J WeisdorfDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
J S MillerDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USBeckman Research InstituteKarolinska University Hospital · SEUniversity of Bergen · NO

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
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)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
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
CMVPepVax to Protect HCT Recipients from Cytomegalovirus InfectionR01CA181045 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI DIAMOND, DON J · 2014 to 2018
$3.6M
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 TR000114NCI NIH HHS 1R01 CA181045NCI NIH HHS 5R01 CA077544NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS P30 CA033572NCI NIH HHS P30CA033572NCI NIH HHS P30 CA077598NCI NIH HHS P30 CA77598NCI NIH HHS R01 CA072669NCI NIH HHS R01 CA077544NCI NIH HHS R01 CA181045NCI NIH HHS R01CA72669NCI NIH HHS R35 CA197292NHLBI NIH HHS R01 HL122216
6 · The paper itself

Abstract

We have recently described a specialized subset of human natural killer (NK) cells with a CD56(dim)CD57(+)NKG2C(+) phenotype that expand specifically in response to cytomegalovirus (CMV) reactivation in hematopoietic cell transplant (HCT) recipients and exhibit properties characteristic of adaptive immunity. We hypothesize that these cells mediate relapse protection and improve post-HCT outcomes. In 674 allogeneic HCT recipients, we found that those who reactivated CMV had lower leukemia relapse (26% (17-35%), P=0.05) and superior disease-free survival (DFS) (55% (45-65%) P=0.04) 1 year after reduced intensity conditioning (RIC) compared with CMV seronegative recipients who experienced higher relapse rates (35% (27-43%)) and lower DFS (46% (38-54%)). This protective effect was independent of age and graft-vs-host disease and was not observed in recipients who received myeloablative regimens. Analysis of the reconstituting NK cells demonstrated that CMV reactivation is associated with both higher frequencies and greater absolute numbers of CD56(dim)CD57(+)NKG2C(+) NK cells, particularly after RIC HCT. Furthermore, expansion of these cells at 6 months posttransplant independently trended toward a lower 2-year relapse risk. Together, our data suggest that the protective effect of CMV reactivation on posttransplant relapse is in part driven by adaptive NK cell responses.

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAdultCD56 AntigenCD57 AntigensCell Line, TumorCytomegalovirusFemaleHumansKiller Cells, NaturalLeukemiaMaleMiddle AgedMonocytesNK Cell Lectin-Like Receptor Subfamily CRecurrenceCD56 AntigenCD57 AntigensKLRC2 protein, humanNCAM1 protein, humanNK Cell Lectin-Like Receptor Subfamily C

Identifiers

PMID26416461
PMCPMC4740203
OpenAlexW1839618459

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.