Evidence map›Paper›PMID 26908740›Full record

Trial reportThe Journal of infectious diseases2016

Utility of the Enzyme-Linked Immunospot Interferon-γ-Release Assay to Predict the Risk of Cytomegalovirus Infection in Hematopoietic Cell Transplant Recipients.

Lior Nesher, Dimpy P Shah, Ella J Ariza-Heredia, Jacques M Azzi, Hala K Siddiqui, Shasank S Ghantoji, Lisa Y Marsh, Lamprinos Michailidis, George Makedonas, Katy Rezvani and 2 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 75 citations in OpenAlex.

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  11. Cytomegalovirus (CMV) Reactivation and CMV-Specific Cell-Mediated Immunity After Chimeric Antigen Receptor T-Cell Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
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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

12 authors at 2 institutions in 1 country.

Lior NesherDepartment of Infectious Diseases, Infection Control, and Employee Health.
Dimpy P ShahDepartment of Infectious Diseases, Infection Control, and Employee Health.
Ella J Ariza-HerediaDepartment of Infectious Diseases, Infection Control, and Employee Health.
Jacques M AzziDepartment of Infectious Diseases, Infection Control, and Employee Health.
Hala K SiddiquiDepartment of Infectious Diseases, Infection Control, and Employee Health.
Shasank S GhantojiDepartment of Infectious Diseases, Infection Control, and Employee Health.
Lisa Y MarshDepartment of Infectious Diseases, Infection Control, and Employee Health.
Lamprinos MichailidisDepartment of Infectious Diseases, Infection Control, and Employee Health.
George MakedonasCenter for Human Immunobiology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Katy RezvaniDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center.
Elizabeth J ShpallDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center.
Roy F ChemalyDepartment of Infectious Diseases, Infection Control, and Employee Health.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
PR1-specific CB T cells for Patients with Myeloid MalignanciesP01CA148600 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MOLLDREM, JEFFREY J · 2011 to 2022
$24.4M
NCI NIH HHS P01 CA148600NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The ability to distinguish allogeneic hematopoietic cell transplant (allo-HCT) recipients at risk for cytomegalovirus (CMV) reactivation from those who are not is central for optimal CMV management strategies. Interferon γ (IFN-γ) produced by CMV-challenged T cells may serve as an immune marker differentiating these 2 populations. We prospectively monitored 63 CMV-seropositive allo-HCT recipients with a CMV-specific enzyme-linked immunospot (ELISPOT) assay and for CMV infection from the period before transplantation to day 100 after transplantation. Assay results above certain thresholds (50 spots per 250 000 cells for immediate early 1 or 100 spots per 250 000 cells for phosphoprotein 65) identified patients who were protected against CMV infection as long as they had no graft-versus-host disease and/or were not receiving systemic corticosteroids. Based on the multivariable Cox proportional hazards regression model, the only significant factor for preventing CMV reactivation was a CMV-specific ELISPOT response above the determined thresholds (adjusted hazard ratio, 0.21; 95% confidence interval, .05-.97; P = .046). Use of this assay as an additional tool for managing allo-HCT recipients at risk for CMV reactivation needs further validation in future studies. Application of this new approach may reduce the duration and intensity of CMV monitoring and the duration of prophylaxis or treatment with antiviral agents in those who have achieved CMV-specific immune reconstitution.

Indexed as

Enzyme-Linked Immunospot AssayHematopoietic Stem Cell TransplantationInterferon-gamma Release TestsTransplant RecipientsAdultAgedBiomarkersCohort StudiesCytomegalovirus InfectionsFemaleHumansInterferon-gammaLeukemiaMaleMiddle AgedProspective StudiesBiomarkersInterferon-gammabone marrow transplantcytomegalovirusELISPOTIGRAstem cell transplant

Identifiers

PMID26908740
PMCPMC4857477
OpenAlexW2309520817

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.