Evidence map›Paper›PMID 26680375›Full record

ArticleTransplantation2016

Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients.

Ajit P Limaye, Corinna La Rosa, Jeff Longmate, Don J Diamond

Open access · greenAbstract read
In one paragraph

Article in Transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Human Cytomegalovirus Interleukin 10 Homologs: Facing the Immune System.Frontiers in cellular and infection microbiology · 2020
    Review
  6. Article
  7. Article
  8. Article
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

4 authors at 2 institutions in 1 country.

Ajit P Limaye1 Department of Medicine, Division of Infectious Diseases, University of Washington Medical Center, Seattle, WA.2 Department of Experimental Therapeutics, Beckman Research Institute of the City of Hope, City of Hope Comprehensive Cancer Center, Duarte, CA.3 Division of Biostatistics, Beckman Research Institute of the City of Hope, City of Hope Comprehensive Cancer Center, Duarte, CA.
Corinna La Rosa
Jeff Longmate
Don J Diamond
City of Hope · USUniversity of Washington Medical Center · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
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
IL-10 & PD-1 Modulation to Reduce CMV Disease Incidence in Solid Organ RecipientsR21AI084019 · NIAID · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI LA ROSA, CORINNA, LIMAYE, ABHIJIT PRAKASH · 2009 to 2010
$461k
NCI NIH HHS CA33572NCI NIH HHS P01 CA030206NCI NIH HHS P01-CA30206NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA077544NCI NIH HHS R01-CA77544NIAID NIH HHS R21 AI084019
6 · The paper itself

Abstract

backgroundImmune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk.

methodsPlasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT: 13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation.

resultsIL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity.

conclusionsThe exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.

Indexed as

Transplant RecipientsAntiviral AgentsBiomarkersCytomegalovirus InfectionsDrug Administration ScheduleDrug MonitoringEnzyme-Linked Immunosorbent AssayGanciclovirHumansInterleukin-10Kidney TransplantationLiver TransplantationPredictive Value of TestsProspective StudiesRisk AssessmentRisk FactorsAntiviral AgentsBiomarkersGanciclovirIL10 protein, humanInterleukin-10Valganciclovir

Identifiers

PMID26680375
PMCPMC4685744
OpenAlexW2316978073

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.