Evidence map›Paper›PMID 32131853›Full record

ArticleJournal of translational medicine2020

A novel TLR7 agonist as adjuvant to stimulate high quality HBsAg-specific immune responses in an HBV mouse model.

Yunlong Hu, Li Tang, Zhengyu Zhu, He Meng, Tingting Chen, Sheng Zhao, Zhenchao Jin, Zhulin Wang, Guangyi Jin

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. The progress of molecules and strategies for the treatment of HBV infection.Frontiers in cellular and infection microbiology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Roles of TLR7 inFrontiers in cellular and infection microbiology · 2021
    Article
  13. Article
  14. Review
  15. 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

9 authors at 2 institutions in 1 country.

Yunlong HuThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China. jackyhu@126.com.
Li TangThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China.
Zhengyu ZhuShenzhen Kang Tai Biological Products CO., Ltd, Shenzhen, 518060, China.
He MengDepartment of Stomatology, Shenzhen University General Hospital & Shenzhen University Clinical Medical Academy, Shenzhen, 518055, China.
Tingting ChenThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China.
Sheng ZhaoThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China.
Zhenchao JinThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China.
Zhulin WangThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China.
Guangyi JinThe Cancer Research Center, School of Medicine, Shenzhen University, Shenzhen, 518055, China. gyjin@szu.edu.cn.
Shenzhen University · CNShenzhen Weiguang Biological Products (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe global burden of hepatitis B virus (HBV) infection in terms of morbidity and mortality is immense. Novel treatments that can induce a protective immune response are urgently needed to effectively control the HBV epidemic and eventually eradicate chronic HBV infection.

methodsWe designed and evaluated an HBV therapeutic vaccine consisting of a novel Toll-like receptor 7 (TLR7) agonist T7-EA, an Alum adjuvant and a recombinant HBsAg protein. We used RNA-seq, ELISA and hTLR7/8 reporting assays to characterize T7-EA in vitro and real-time PCR to evaluate the tissue-retention characteristics in vivo. To evaluate the adjuvant potential, we administrated T7-EA intraperitoneally in a formulation with an Alum adjuvant and HBsAg in normal and HBV mice, then, we evaluated the HBsAg-specific immune responses by ELISA and Elispot assays.

resultsT7-EA acted as an hTLR7-specific agonist and induced a similar gene expression pattern as an unmodified TLR7 ligand when Raw 264.7 cells were exposed to T7-EA; however, T7-EA was more potent than the unmodified TLR7 ligand. In vivo studies showed that T7-EA had tissue-retaining activity with stimulating local cytokine and chemokine expression for up to 7 days. T7-EA could induce Th1-type immune responses, as evidenced by an increased HBsAg-specific IgG2a titer and a T-cell response in normal mice compared to mice received traditional Alum-adjuvant HBV vaccine. Importantly, T7-EA could break immune tolerance and induce persistent HBsAg-specific antibody and T-cell responses in an HBV mouse model.

conclusionsT7-EA might be a candidate adjuvant in a prophylactic and therapeutic HBV vaccine.

Indexed as

Hepatitis B Surface AntigensHepatitis B virusAdjuvants, ImmunologicAnimalsHepatitis B AntibodiesHepatitis B VaccinesImmunityMiceMice, Inbred BALB CToll-Like Receptor 7Adjuvants, ImmunologicHepatitis B AntibodiesHepatitis B Surface AntigensHepatitis B VaccinesToll-Like Receptor 7AdjuvantHepatitis B Virus (HBV)Toll-like receptor 7 agonistVaccine

Identifiers

PMID32131853
PMCPMC7055022
OpenAlexW3012277947

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.