Evidence map›Paper›PMID 32595636›Full record

ReviewFrontiers in immunology2020

The Use of Toll-Like Receptor Agonists in HIV-1 Cure Strategies.

Janne Tegder Martinsen, Jesper Damsgaard Gunst, Jesper Falkesgaard Højen, Martin Tolstrup, Ole Schmeltz Søgaard

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
5.6field-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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Janne Tegder MartinsenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Jesper Damsgaard GunstDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Jesper Falkesgaard HøjenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Ole Schmeltz SøgaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are a family of pattern recognition receptors and part of the first line of defense against invading microbes. In humans, we know of 10 different TLRs, which are expressed to varying degrees in immune cell subsets. Engaging TLRs through their specific ligands leads to activation of the innate immune system and secondarily priming of the adaptive immune system. Because of these unique properties, TLR agonists have been investigated as immunotherapy in cancer treatment for many years, but in recent years there has also been growing interest in the use of TLR agonists in the context of human immunodeficiency virus type 1 (HIV-1) cure research. The primary obstacle to curing HIV-1 is the presence of a latent viral reservoir in transcriptionally silent immune cells. Due to the very limited transcription of the integrated HIV-1 proviruses, latently infected cells cannot be targeted and cleared by immune effector mechanisms. TLR agonists are very interesting in this context because of their potential dual effects as latency reverting agents (LRAs) and immune modulatory compounds. Here, we review preclinical and clinical data on the impact of TLR stimulation on HIV-1 latency as well as antiviral and HIV-1-specific immunity. We also focus on the promising role of TLR agonists in combination strategies in HIV-1 cure research. Different combinations of TLR agonists and broadly neutralizing antibodies or TLRs agonists as adjuvants in HIV-1 vaccines have shown very encouraging results in non-human primate experiments and these concepts are now moving into clinical testing.

Indexed as

HIV-1Adjuvants, ImmunologicAIDS VaccinesAnimalsAnti-HIV AgentsBroadly Neutralizing AntibodiesClinical Trials as TopicHIV AntibodiesHIV InfectionsHumansImmune Checkpoint InhibitorsImmunologic FactorsImmunotherapyIn Vitro TechniquesModels, ImmunologicalPrimatesAdjuvants, ImmunologicAIDS VaccinesAnti-HIV AgentsBroadly Neutralizing AntibodiesHIV AntibodiesImmune Checkpoint InhibitorsImmunologic FactorsPteridinesTLR3 protein, humanTLR7 protein, humanTLR9 protein, humanToll-Like Receptor 3Toll-Like Receptor 7Toll-Like Receptor 9Toll-Like ReceptorsvesatolimodHIV-1HIV-1 cureHIV-1 vaccineimmune modulationinnate immunitylatency reversing agentsTLR

Identifiers

PMID32595636
PMCPMC7300204
OpenAlexW3030947224

What OpenQuestion holds

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LicenceCC BY
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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.