Evidence map›Paper›PMID 32076709›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Cytomegalovirus (CMV) Cell-Mediated Immunity and CMV Infection After Allogeneic Hematopoietic Cell Transplantation: The REACT Study.

Roy F Chemaly, Lynn El Haddad, Drew J Winston, Scott D Rowley, Kathleen M Mulane, Pranatharthi Chandrasekar, Robin K Avery, Parameswaran Hari, Karl S Peggs, Deepali Kumar and 8 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

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  15. Current and Future Strategies for the Prevention and Treatment of Cytomegalovirus Infections in Transplantation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 14 institutions in 4 countries.

Roy F ChemalyDepartment of Infectious Diseases, Infection Control, and Employee Health, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Lynn El HaddadDepartment of Infectious Diseases, Infection Control, and Employee Health, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Drew J WinstonRonald Reagan UCLA Medical Center, Los Angeles, California, USA.
Scott D RowleyHackensack University Medical Center, New Jersey, USA.
Kathleen M MulaneDepartment of Medicine, University of Chicago, Chicago, Illinois, USA.
Pranatharthi ChandrasekarDivision of Infectious Diseases, Department of Medicine, Wayne State University, Detroit, Michigan, USA.
Robin K AveryDivision of Infectious Diseases (Transplant Oncology), Johns Hopkins University, Baltimore, Maryland, USA.
Parameswaran HariDivision of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Karl S PeggsDepartment of Haematology, University College London Cancer Institute and University College London Hospitals National Health Service Foundation Trust, London, United Kingdom.
Deepali KumarTransplant Infectious Diseases, University Health Network, Toronto, Ontario, Canada.
Rajneesh NathBone Marrow Transplant, Banner MD Anderson Cancer Center, Gilbert, Arizona, USA.
Per LjungmanDepartment of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Sherif B MossadDepartment of Infectious Diseases, Respiratory Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Sanjeet S DadwalDivision of Infectious Diseases, City of Hope, Duarte, California, USA.
Ted BlanchardOxford Immunotec USA, Inc, Charlotte, North Carolina, USA.
Dimpy P ShahDepartment of Epidemiology and Biostatistics, University of Texas Health, San Antonio, Texas, USA.
Ying JiangDepartment of Infectious Diseases, Infection Control, and Employee Health, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ella Ariza-HerediaDepartment of Infectious Diseases, Infection Control, and Employee Health, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · USCity of Hope · USCleveland Clinic · USEvotec (United States) · USHackensack University Medical Center · USJohns Hopkins University · USKarolinska Institutet · SEMedical College of Wisconsin · USRonald Reagan UCLA Medical Center · USThe University of Texas Health Science Center at San Antonio · USUniversity College London Hospitals NHS Foundation Trust · GBUniversity Health Network · CAUniversity of Chicago · USWayne State University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundCytomegalovirus (CMV) infection remains an important cause of morbidity and mortality in allogeneic hematopoietic cell transplant (allo-HCT) recipients. CMV cell-mediated immunity (CMV-CMI) as determined by a peptide-based enzyme-linked immunospot (ELISPOT) CMV assay may identify patients at risk for clinically significant CMV infection (CS-CMVi).

methodsThe CS-CMVi was defined as CMV viremia and/or disease necessitating antiviral therapy. CMV-CMI was characterized as high when the intermediate-early 1 (IE-1) antigen spot counts (SPCs) were >100 (cutoff 1) or when the IE-1 and phosphoprotein 65 antigen SPCs were both >100 SPCs per 250 000 cells (cutoff 2), and a low CMV-CMI when SPCs were below these thresholds. In this prospective multicenter study, we evaluated CMV-CMI every 2 weeks from the pretransplant period until 6 months posttransplantation in 241 allo-HCT recipients with positive CMV serostatus. The primary endpoint was CS-CMVi occurring within 2 weeks of the last measurement of CMV-CMI.

resultsCS-CMVi occurred in 70 allo-HCT recipients (29%). CMV-CMI was low in patients who experienced CS-CMVi (94%), whereas those who had a high CMV-CMI were less likely to have CS-CMVi (P < .0001). Patients with CS-CMVi had higher all-cause mortality (P = .007), especially those with low CMV-CMI (P = .035). On multivariable analysis, CMV-CMI, sex, race, antithymocyte globulin, and steroid use were independent predictors of CS-CMVi, and the time from transplant to engraftment was the only predictor of mortality.

conclusionsMeasurement of CMV-CMI using a novel ELISPOT assay would be useful clinically to monitor allo-HCT recipients and distinguish between those at risk of developing CS-CMVi and requiring antiviral prophylaxis or therapy and those who are protected.

Indexed as

Cytomegalovirus InfectionsHematopoietic Stem Cell TransplantationAntiviral AgentsCytomegalovirusHumansImmunity, CellularProspective StudiesAntiviral Agentscell-mediated immunityCMV ELISPOT assaycytomegalovirushematopoietic cell transplantmulticenter

Identifiers

PMID32076709
PMCPMC7713694
OpenAlexW3008607427

What Socratic 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 Socratic graph.