Evidence map›Paper›PMID 31580403›Full record

ArticleBritish medical bulletin2019

Advances in the treatment of cytomegalovirus.

B A Krishna, M R Wills, J H Sinclair

Open access · hybridAbstract read
In one paragraph

Article in British medical bulletin, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
6.5field-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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  11. Digital PCR-Based Genotyping: A Precision Approach to HCMV Drug Resistance.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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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

3 authors at 2 institutions in 2 countries.

B A KrishnaDepartment of Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
M R WillsDepartment of Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
J H SinclairDepartment of Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
Addenbrooke's Hospital · GBUniversity of Cambridge · GB

Funding

Medical Research Council MR/S00081X/1Wellcome Trust
6 · The paper itself

Abstract

backgroundHuman cytomegalovirus (HCMV) is a threat to immunologically weak patients. HCMV cannot yet be eliminated with a vaccine, despite recent advances. SOURCES OF DATA: Sources of data are recently published research papers and reviews about HCMV treatments. AREAS OF AGREEMENT: Current antivirals target the UL54 DNA polymerase and are limited by nephrotoxicity and viral resistance. Promisingly, letermovir targets the HCMV terminase complex and has been recently approved by the FDA and EMA. AREAS OF CONTROVERSY: Should we screen newborns for HCMV, and use antivirals to treat sensorineural hearing loss after congenital HCMV infection? GROWING POINTS: Growing points are developing drugs against latently infected cells. In addition to small molecule inhibitors, a chemokine-based fusion toxin protein, F49A-FTP, has shown promise in killing both lytically and latently infected cells. AREAS TIMELY FOR DEVELOPING RESEARCH: We need to understand what immune responses are required to control HCMV, and how best to raise these immune responses with a vaccine.

Indexed as

Antiviral AgentsCytomegalovirusCytomegalovirus InfectionsCytomegalovirus VaccinesDrug DevelopmentEarly DiagnosisHematopoietic Stem Cell TransplantationHumansImmunity, CellularImmunoglobulinsImmunosuppression TherapyInfant, NewbornOrgan TransplantationPerinatal CareVirus LatencyAntiviral AgentsCytomegalovirus VaccinesImmunoglobulinsantiviralshuman cytomegalovirusinfectionlatencyvaccines

Identifiers

PMID31580403
PMCPMC6821982
OpenAlexW2970771745

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.