Evidence map›Paper›PMID 30241300›Full record

ArticleVaccines2018

Virus-Like Particles Are a Superior Platform for Presenting M2e Epitopes to Prime Humoral and Cellular Immunity against Influenza Virus.

Ki-Hye Kim, Young-Man Kwon, Young-Tae Lee, Min-Chul Kim, Hye Suk Hwang, Eun-Ju Ko, Youri Lee, Hyo-Jick Choi, Sang-Moo Kang

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Virus-like Particles for TEM Regulation and Antitumor Therapy.Journal of functional biomaterials · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. 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

9 authors at 3 institutions in 3 countries.

Ki-Hye KimInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. kihyekim4282@gmail.com.
Young-Man KwonInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. ymankwon@gmail.com.
Young-Tae LeeInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. leechard75@gmail.com.
Min-Chul KimInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. mckim001@gmail.com.
Hye Suk HwangInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. hshwang33@gmail.com.
Eun-Ju KoInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. ej.ko226@gmail.com.
Youri LeeInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. youl6248@gmail.com.
Hyo-Jick ChoiDepartment of Chemical and Materials Engineering, University of Alberta, Edmonton, AB T6G 2V4, Canada. hyojick@ualberta.ca.ORCID 0000-0001-8233-5864
Sang-Moo KangInstitute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA. skang24@gsu.edu.
Georgia State University · USNational Institutes of Health · USUniversity of Alberta · CA

Funding

Influenza vaccines inducing broadly cross protective immunityR01AI093772 · NIAID · GEORGIA STATE UNIVERSITY · PI KANG, SANG-MOO · 2011 to 2020
$4.2M
VLP Vaccine TechnologyR01AI105170 · NIAID · GEORGIA STATE UNIVERSITY · PI KANG, SANG-MOO · 2013 to 2017
$3.7M
New RSV Vaccines with Improved Safety and EfficacyR41AI134132 · NIAID · ADVAC, LLC · PI KANG, SANG-MOO · 2018 to 2018
$225k
Foundation for the National Institutes of Health AI105170, AI1093772, AI119366NIAID NIH HHS R01 AI093772NIAID NIH HHS R01 AI105170NIAID NIH HHS R41 AI134132
6 · The paper itself

Abstract

Influenza virus M2 protein has a highly conserved ectodomain (M2e) as a cross-protective antigenic target. We investigated the antigenic and immunogenic properties of tandem repeat M2e (5xM2e) proteins and virus-like particles (5xM2e VLP) to better understand how VLP and protein platform vaccines induce innate and protective adaptive immune responses. Despite the high antigenic properties of 5xM2e proteins, the 5xM2e VLP was superior to 5xM2e proteins in inducing IgG2a isotype antibodies, T cell responses, plasma cells and germinal center B cells as well as in conferring cross protection. Mice primed with 5xM2e VLP were found to be highly responsive to 5xM2e protein boost, overcoming the low immunogenicity and protective efficacy of 5xM2e proteins. Immunogenic differences between VLPs and proteins in priming immune responses might be due to an intrinsic ability of 5xM2e VLP to stimulate dendritic cells secreting T helper type 1 (Th1) cytokines. We also found that 5xM2e VLP was effective in inducing inflammatory cytokines and chemokines, and in recruiting macrophages, monocytes, neutrophils, and CD11b⁺ dendritic cells at the injection site. Therefore, this study provides evidence that 5xM2e VLP is an effective vaccine platform, inducing cross-protection by stimulating innate and adaptive immune responses.

Indexed as

5xM2e epitopesinnate/adaptive immunitypriming effectvirus-like particles (VLP), cross-protection

Identifiers

PMID30241300
PMCPMC6313937
OpenAlexW2890115379

What OpenQuestion 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 OpenQuestion graph.