Evidence map›Paper›PMID 32443313›Full record

Observational studyMedicine2020

Soluble PD-L1: a potential immune marker for HIV-1 infection and virological failure.

José Avendaño-Ortiz, Marina Rubio-Garrido, Roberto Lozano-Rodríguez, Jorge Del Romero, Carmen Rodríguez, Santiago Moreno, Luis A Aguirre, África Holguín, Eduardo López-Collazo

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Regulation of PD-L1 Expression by Nuclear Receptors.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

9 authors at 4 institutions in 2 countries.

José Avendaño-OrtizInnate Immunity Group.
Marina Rubio-GarridoHIV-1 Molecular Epidemiology Laboratory, Ramón y Cajal University Hospital-IRYCIS and CIBERESP-RITIP.
Roberto Lozano-RodríguezInnate Immunity Group.
Jorge Del RomeroSandoval Health Center, Madrid.
Carmen RodríguezSandoval Health Center, Madrid.
Santiago MorenoHIV-1 Molecular Epidemiology Laboratory, Ramón y Cajal University Hospital-IRYCIS and CIBERESP-RITIP.
Luis A AguirreInnate Immunity Group.
África HolguínHIV-1 Molecular Epidemiology Laboratory, Ramón y Cajal University Hospital-IRYCIS and CIBERESP-RITIP.
Eduardo López-CollazoInnate Immunity Group.
Innate Pharma (France) · FRCentro de Investigación Biomédica en Red de Epidemiología y Salud Pública · ESMadrid Health Service · ESInstituto Cajal · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite viral control, basal chronic inflammation and its related comorbidities remain unsolved problems among HIV-infected individuals. Soluble factors derived from myeloid cells have emerged as potent markers associated with HIV-related comorbidities and mortality. In the present report, we explored the relationship between soluble programmed death-ligand 1 (sPD-L1) and HIV-1 infection, antiretroviral therapy (ART), CD4/CD8 ratio, viral load (VL), and sexually transmitted coinfections.A prospective observational study on 49 HIV-1 infected adults.We found sPD-L1 levels were significantly higher in 49 HIV infected subjects than in 30 uninfected adults (1.05 ng/ml vs 0.52 ng/ml; P < .001). In this line, sPD-L1 levels were found to be elevated in 16 HIV infected subjects with undetectable VL compared with the uninfected subjects (0.75 ng/ml vs 0.52 ng/ml; P = .02). Thirteen ART-treated individuals with virological failure exhibited the highest sPDL1 levels, which were significantly higher than both 20 ART naïve infected individuals (1.68 ng/ml vs 0.87 ng/ml; P = .003) and the 16 ART-treated individuals with suppressed viremia (1.68 ng/ml vs 0.79 ng/ml; P = 002). Entire cohort data showed a statistically significant positive correlation between VL and sPD-L1 levels in plasma (r = 0.3; P = 036).Our findings reveal sPDL-1 as a potential biomarker for HIV infection especially interesting in those individuals with virological failure.

Indexed as

HIV-1AdultAnti-HIV AgentsB7-H1 AntigenBiomarkersFemaleHIV InfectionsHumansMaleMiddle AgedProspective StudiesViral LoadAnti-HIV AgentsB7-H1 AntigenBiomarkersCD274 protein, human

Identifiers

PMID32443313
PMCPMC7254573
OpenAlexW3026530809

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.