Evidence map›Paper›PMID 19369230›Full record

ArticleBlood2009

Impact of donor CMV status on viral infection and reconstitution of multifunction CMV-specific T cells in CMV-positive transplant recipients.

Wendi Zhou, Jeff Longmate, Simon F Lacey, Joycelynne M Palmer, Ghislaine Gallez-Hawkins, Lia Thao, Ricardo Spielberger, Ryotaro Nakamura, Stephen J Forman, John A Zaia and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

65 citing papers in PubMed, 147 citations in OpenAlex.

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  8. Cytomegalovirus viral load and virus-specific immune reconstitution after peripheral blood stem cell versus bone marrow transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2012
    Trial
  9. Article
  10. Assessing the significance of cytomegalovirus reactivation in recipients of allogeneic hematopoietic stem cell transplantation: a cohort study.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
    Observational
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5 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

11 authors at 2 institutions in 1 country.

Wendi ZhouDepartment of Virology, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Jeff Longmate
Simon F Lacey
Joycelynne M Palmer
Ghislaine Gallez-Hawkins
Lia Thao
Ricardo Spielberger
Ryotaro Nakamura
Stephen J Forman
John A Zaia
Don J Diamond
City of Hope · USBeckman Research Institute

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
ZOPOLRESTAT IN NORMOTENSIVE, TYPE 1 DIA WITH INCIPIENT NEPHROPATHYM01RR000043 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZAIA, JOHN A · 1985 to 2010
$76.4M
Vaccine-Induced Immunity to CMVP01CA030206 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI FORMAN, STEPHEN J · 1985 to 2010
$31.8M
Peptide Vaccine To Prevent CMV Disease After HSCTR01CA077544 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI DIAMOND, DON J · 1998 to 2017
$5.6M
Evaluation New Targets of CMV Cellular ImmunityR01AI058148 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ZAIA, JOHN A · 2004 to 2007
$1.7M
Evaluating New Targets of CMV Cellular ImmunityR01CA145207 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ZAIA, JOHN A · 2010 to 2013
$1.6M
CLINICAL EVALUATION OF A POXVIRUS VACCINE TARGETING P53R21CA114889 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ELLENHORN, JOSHUA D.I. · 2005 to 2006
$594k
CpG DNA:Epitope Fusion Peptide Conjugates as HIV VaccineR21AI062496 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI DIAMOND, DON J · 2005 to 2006
$467k
Criteria for Protective Immunity to BK virus in Kidney Transplant RecipientsR21DK077374 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI LACEY, SIMON F · 2006 to 2007
$467k
NCI NIH HHS CA030206NCI NIH HHS CA033572NCI NIH HHS CA077544NCI NIH HHS CA114889NCI NIH HHS P01 CA030206NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA077544NCI NIH HHS R01 CA145207NCI NIH HHS R21 CA114889NCRR NIH HHS M01 RR000043NCRR NIH HHS M01-RR00043-39NIAID NIH HHS AI058148NIAID NIH HHS AI062496NIAID NIH HHS R01 AI058148NIAID NIH HHS R21 AI062496NIDDK NIH HHS DK077374NIDDK NIH HHS R21 DK077374
6 · The paper itself

Abstract

Reconstitution of cytomegalovirus (CMV)-specific CD8(+) T cells is essential to the control of CMV infection in CMV-positive recipients (R(+)) after allogeneic hematopoietic stem cell transplantation (HCT). Six-color flow cytometry was used to assess the functional profile of CMV-specific CD8(+) T cells in 62 of 178 R(+) HCT recipients followed virologically for CMV reactivation. R(+) recipients receiving grafts from CMV-negative donors (D(-); D(-)/R(+)) reconstituted fewer multifunctional CD8(+) T cells expressing tumor necrosis factor-alpha (TNF-alpha), macrophage inflammatory protein-1beta (MIP-1beta), and CD107 in addition to interferon-gamma (IFN-gamma), compared with D(+)/R(+) recipients. Unlike monofunctional CD8(+) T cells secreting IFN-gamma, which were abundantly generated during CMV reactivation in D(-)/R(+) recipients, the relative lack of multifunctional CD8(+) T cells persisted until at least 1 year post-HCT. D(-)/R(+) recipients were more likely to require recurrent and prolonged use of antivirals. These findings were robust to statistical adjustment for pretransplant factors, as well as for posttransplant factors including graft-versus-host disease (GVHD) and its treatment by steroids. These analyses suggest that D(+)/R(+) transplants, on average, generate higher levels of multifunctional CMV-specific T cells and require less antiviral therapy compared with D(-)/R(+) HCT recipients. These results highlight the benefit of D(+) donors in improving outcomes of R(+) HCT recipients by reducing the duration and recurrent need of antiviral treatment, aided by increased levels of multifunctional CMV-specific T cells.

Indexed as

T-Cell Antigen Receptor SpecificityTissue DonorsAdultAntiviral AgentsBone Marrow TransplantationCD8-Positive T-LymphocytesCohort StudiesCytokinesCytomegalovirusCytomegalovirus InfectionsCytomegalovirus VaccinesDisease Transmission, InfectiousFemaleGraft SurvivalHematologic NeoplasmsHumansAntiviral AgentsCytokinescytomegalovirus matrix protein 65kDaCytomegalovirus VaccinesPhosphoproteinsViral Matrix Proteins

Identifiers

PMID19369230
PMCPMC2710937
OpenAlexW1994888472

What OpenQuestion holds

Textmetadata
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.