Evidence map›Paper›PMID 33918831›Full record

ArticleViruses2021

Treatment with the Immunomodulator AIC649 in Combination with Entecavir Produces Antiviral Efficacy in the Woodchuck Model of Chronic Hepatitis B.

Kyle E Korolowicz, Manasa Suresh, Bin Li, Xu Huang, Changsuek Yon, Xuebing Leng, Bhaskar V Kallakury, Robin D Tucker, Stephan Menne

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 11 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

9 authors at 1 institution in 1 country.

Kyle E KorolowiczDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0003-1116-6500
Manasa SureshDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0002-1285-0374
Bin LiDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.
Xu HuangDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.
Changsuek YonDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.
Xuebing LengDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0001-6884-4910
Bhaskar V KallakuryDepartment of Pathology, Georgetown University Medical Center, Washington, DC 20057, USA.
Robin D TuckerDivision of Comparative Medicine, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0003-0081-4752
Stephan MenneDepartment of Microbiology & Immunology, Georgetown University Medical Center, Washington, DC 20057, USA.ORCID 0000-0001-6873-4084
Georgetown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As current interventions for chronic hepatitis B (CHB) rarely induce cure, more effective drugs are needed. Short-term treatment of woodchucks with the novel immunomodulator AIC649, a parapoxvirus-based stimulator of toll-like receptor 9 dependent and independent pathways, has been shown to reduce viral DNA and surface antigen via a unique, biphasic response pattern. The present study evaluated long-term AIC649 treatment in combination with Entecavir for potency and safety in woodchucks. AIC649 monotreatment induced modest reductions in serum viral DNA and surface and e antigens that were associated with the same biphasic response pattern previously observed. Entecavir monotreatment reduced transiently viremia but not antigenemia, while AIC649/Entecavir combination treatment mediated superior viral control. Undetectability of viral antigens and elicitation of antibodies in AIC649/Entecavir-treated woodchucks correlated with the expression of interferons and suppression of viral replication in liver. Combination treatment was well tolerated, and liver enzyme elevations were minor and transient. It was concluded that the AIC649-mediated effects were most likely based on an improvement and/or reconstitution of antiviral immune responses that are typically deficient in CHB. As a combination partner to Entecavir, the antiviral efficacy of AIC649 was markedly enhanced. This preclinical study supports future evaluation of AIC649 for treatment of human CHB.

Indexed as

AnimalsAntiviral AgentsDisease Models, AnimalDNA, ViralDrugs, InvestigationalGuanineHepatitis B, ChronicHepatitis B Virus, WoodchuckImmunologic FactorsMarmotaTreatment OutcomeViremiaVirus ReplicationAntiviral AgentsDNA, ViralDrugs, InvestigationalentecavirGuanineImmunologic Factorsantiviral efficacychronic hepatitis Bentecavirimmune responseparapoxvirusTLR9woodchuck

Identifiers

PMID33918831
PMCPMC8069054
OpenAlexW3154491292

What Socratic holds

Textmetadata
LicenceCC BY
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.