Evidence map›Paper›PMID 39951015›Full record

ArticleAIDS (London, England)2025

Soluble CD14 and IL-12p70 on early antiretroviral therapy predict HIV load setpoint after treatment interruption.

Pien M van Paassen, Anders C Boyd, Alexander O Pasternak, Irma Maurer, Agnes M Harskamp, Marlous L Grijsen, Suzanne Jurriaans, Jan M Prins, Neeltje A Kootstra, Godelieve J de Bree

Abstract read
In one paragraph

Article in AIDS (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Trial
  2. Review
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

10 authors.

Pien M van PaassenLaboratory for Viral Immune Pathogenesis, Department of Experimental Immunology, Amsterdam UMC, University of Amsterdam.
Anders C BoydAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam.
Alexander O PasternakAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam.
Irma MaurerLaboratory for Viral Immune Pathogenesis, Department of Experimental Immunology, Amsterdam UMC, University of Amsterdam.
Agnes M HarskampLaboratory for Viral Immune Pathogenesis, Department of Experimental Immunology, Amsterdam UMC, University of Amsterdam.
Marlous L GrijsenOxford University Clinical Research Unit Indonesia (OUCRU ID), Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Suzanne JurriaansAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam.
Jan M PrinsDepartment of Internal Medicine, Division of Infectious Diseases, Amsterdam UMC, Amsterdam, The Netherlands.
Neeltje A KootstraLaboratory for Viral Immune Pathogenesis, Department of Experimental Immunology, Amsterdam UMC, University of Amsterdam.
Godelieve J de BreeDepartment of Internal Medicine, Division of Infectious Diseases, Amsterdam UMC, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAfter analytical treatment interruption (ATI), viral rebound occurs in most people with HIV. The time to viral rebound (TTVR) is likely determined by the properties of the viral reservoir as well as the antiviral immune response. Soluble biomarkers of immune activation may be predictive of TTVR and plasma viral load (pVL) setpoint after ATI. The objective of this study is to identify these soluble biomarkers.

designA retrospective biomarker analysis of the Primo-SHM trial who were treated 24 or 60 weeks during early HIV infection.

methodsThirty-five biomarkers were measured at ATI in 65 participants. Association between biomarkers and reservoir size, TTVR and pVL at setpoint was assessed.

resultsSCD14 correlated to pVL setpoint ( B  = 0.598; P  = 0.004) and lower levels of IL-12p70 to a higher level of pVL setpoint ( B  = -0.448; P  = 0.04). SCD163 correlated to levels of total HIV-DNA ( B  = 0.413; P  = 0.007).

conclusionAn increased pVL setpoint was associated with higher sCD14 and lower IL-12p70 at ATI, and increased total HIV-DNA was associated with higher sCD163 at ATI. SCD14 and sCD163 are biomarkers of monocyte activation, whereas IL-12p70, produced by monocytes, is essential for inducing Th1 responses. This underscores the relation between immune activation and diminished immune control of HIV. Our findings indicate that sCD14 and IL-12p70 could serve as predictive biomarkers for favorable outcomes in cure interventions.

Indexed as

Anti-Retroviral AgentsBiomarkersHIV InfectionsInterleukin-12Lipopolysaccharide ReceptorsViral LoadAdultAntiretroviral Therapy, Highly ActiveFemaleHumansMaleMiddle AgedPlasmaRetrospective StudiesTreatment InterruptionAnti-Retroviral AgentsBiomarkersCD14 protein, humanInterleukin-12Lipopolysaccharide Receptorsantiretroviral therapy interruptionbiomarkersinflammationset pointviral rebound

Identifiers

PMID39951015
PMCPMC12077335

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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.