Evidence map›Paper›PMID 35142488›Full record

ArticleACS chemical biology2022

Structure Guided Design of Bacteriophage Qβ Mutants as Next Generation Carriers for Conjugate Vaccines.

Suttipun Sungsuwan, Xuanjun Wu, Vincent Shaw, Herbert Kavunja, Hunter McFall-Boegeman, Zahra Rashidijahanabad, Zibin Tan, Shuyao Lang, Setare Tahmasebi Nick, Po-Han Lin and 4 more

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  15. Review
  16. Stereoselective Synthesis of Sialyl LewisAngewandte Chemie (International ed. in English) · 2023
    Article
  17. Article
  18. Review
  19. Article
  20. Virus-like Particle Display ofACS infectious diseases · 2022
    Article
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

14 authors at 5 institutions in 4 countries.

Suttipun SungsuwanVirology and Cell Technology Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani 12120, Thailand.
Xuanjun WuNational Glycoengineering Research Center, Shandong Key Laboratory of Carbohydrate Chemistry and Glycobiology, Shandong University, Qingdao, Shandong 266237, China.ORCID 0000-0002-7399-6916
Vincent Shaw
Herbert KavunjaIaso Therapeutics Inc., 4942 Dawn Avenue, East Lansing, Michigan 48823, United States.
Hunter McFall-Boegeman
Zahra Rashidijahanabad
Zibin Tan
Shuyao Lang
Setare Tahmasebi Nick
Po-Han Lin
Zhaojun Yin
Sherif RamadanChemistry Department, Faculty of Science, Benha University, Benha, Qaliobiya 13518, Egypt.ORCID 0000-0002-8639-4105
Xiangshu Jin
Michigan State University · USBenha University · EGIo Therapeutics (United States) · USNational Science and Technology Development Agency · THShandong University · CN

Funding

Generation of active immunity against cytotoxic oligomeric tau speciesR01CA225105 · NCI · MICHIGAN STATE UNIVERSITY · PI HUANG, XUEFEI · 2018 to 2023
$2.8M
Synthetic glycan conjugates with bacteriophage Qbeta for broad spectrum anti-salmonella vaccinesR01AI146210 · NIAID · MICHIGAN STATE UNIVERSITY · PI HUANG, XUEFEI · 2019 to 2023
$1.5M
Development of proprietary bacteriophage Qbeta as a vaccine carrier platform for anti-salmonella vaccineR43AI157185 · NIAID · IASO THERAPEUTICS, INC. · PI KAVUNJA, HERBERT WANJALA · 2021 to 2022
$595k
NCI NIH HHS R01 CA225105NIAID NIH HHS R01 AI146210NIAID NIH HHS R43 AI157185
6 · The paper itself

Abstract

Vaccines are critical tools to treat and prevent diseases. For an effective conjugate vaccine, the carrier is crucial, but few carriers are available for clinical applications. In addition, a drawback of current protein carriers is that high levels of antibodies against the carrier are induced by the conjugate vaccine, which are known to interfere with the immune responses against the target antigen. To overcome these challenges, we obtained the near atomic resolution crystal structure of an emerging protein carrier, i.e., the bacteriophage Qβ virus like particle. On the basis of the detailed structural information, novel mutants of bacteriophage Qβ (mQβ) have been designed, which upon conjugation with tumor associated carbohydrate antigens (TACAs), a class of important tumor antigens, elicited powerful anti-TACA IgG responses and yet produced lower levels of anticarrier antibodies as compared to those from the wild type Qβ-TACA conjugates. In a therapeutic model against an aggressive breast cancer in mice, 100% unimmunized mice succumbed to tumors in just 12 days even with chemotherapy. In contrast, 80% of mice immunized with the mQβ-TACA conjugate were completely free from tumors. Besides TACAs, to aid in the development of vaccines to protect against COVID-19, the mQβ based conjugate vaccine has been shown to induce high levels of IgG antibodies against peptide antigens from the SARS-CoV-2 virus, demonstrating its generality. Thus, mQβ is a promising next-generation carrier platform for conjugate vaccines, and structure-based rational design is a powerful strategy to develop new vaccine carriers.

Indexed as

COVID-19NeoplasmsAllolevivirusAnimalsAntigens, Tumor-Associated, CarbohydrateImmunoglobulin GMiceSARS-CoV-2Vaccines, ConjugateAntigens, Tumor-Associated, CarbohydrateImmunoglobulin GVaccines, Conjugate

Identifiers

PMID35142488
PMCPMC9363528
OpenAlexW4211065228

What OpenQuestion holds

Textmetadata
LicenceTDM
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.