Evidence map›Paper›PMID 36250708›Full record

ArticleJournal of virology2022

cART Restores Transient Responsiveness to IFN Type 1 in HIV-Infected Humanized Mice.

Maarja Gruenbach, Christina K S Muller, Erika Schlaepfer, Luca Baroncini, Doris Russenberger, Nicole P Kadzioch, Benjamin Escher, Martin Schlapschy, Arne Skerra, Simon Bredl and 1 more

Abstract read
In one paragraph

Article in Journal of virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Targeting PD-1Science advances · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. 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

11 authors.

Maarja GruenbachDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Christina K S MullerDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Erika SchlaepferDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Luca BaronciniDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Doris RussenbergerDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Nicole P KadziochDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Benjamin EscherChair of Biological Chemistry, School of Life Sciences, Technical University of Munichgrid.6936.a, Freising, Germany.
Martin SchlapschyChair of Biological Chemistry, School of Life Sciences, Technical University of Munichgrid.6936.a, Freising, Germany.
Arne SkerraChair of Biological Chemistry, School of Life Sciences, Technical University of Munichgrid.6936.a, Freising, Germany.
Simon Bredl *Department of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.
Roberto F Speck *Department of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurichgrid.412004.3, University of Zurichgrid.7400.3, Zurich, Switzerland.ORCID 0000-0002-8453-1137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lack of a human immunodeficiency virus (HIV) cure has heightened interest in immunotherapy. As such, type I interferons (IFNs), in particular, IFN alpha (IFN-α), have gained renewed attention. However, HIV pathogenesis is driven by sustained IFN-mediated immune activation, and the use of IFNs is rather controversial. The following questions therein remain: (i) which IFN-α subtype to use, (ii) at which regimen, and (iii) at what time point in HIV infection it might be beneficial. Here, we used IFN-α14 modified by PASylation for its long half-life

Indexed as

HIV InfectionsInterferon Type IAnimalsAntiviral AgentsHumansInterferon-alphaMiceUbiquitin ThiolesteraseVirus ReplicationAntiviral AgentsInterferon-alphaInterferon Type IUbiquitin ThiolesteraseUSP18 protein, humananalytical treatment interruptionHIVhumanized miceIFN-alpha 12IFN-alpha 14immunotherapylong actingPASylation

Identifiers

PMID36250708
PMCPMC9645216

What OpenQuestion holds

Textmetadata
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.