Evidence map›Paper›PMID 39475238›Full record

ArticlemBio2024

Development of KSHV vaccine platforms and chimeric MHV68-K-K8.1 glycoprotein for evaluating the

Wan-Shan Yang, Dokyun Kim, Soowon Kang, Chih-Jen Lai, Inho Cha, Pei-Ching Chang, Jae U Jung

Abstract read
In one paragraph

Article in mBio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

7 authors.

Wan-Shan YangDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-0661-4033
Dokyun KimDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Soowon KangDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Chih-Jen LaiDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Inho ChaDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Pei-Ching ChangInstitute of Microbiology and Immunology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.ORCID 0000-0001-8665-5494
Jae U JungDepartment of Cancer Biology and Infection Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0003-4559-8774

Funding

KSHV Epigenetic RegulationR01DE023926 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JUNG, JAE U · 2013 to 2024
$4.2M
Development of three KSHV vaccine platforms and chimeric MHV68-K-G for in vivo mouse infection studyU01CA294881 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI Jae U Jung · 2024 to 2026
$2.9M
Tickborne SFTS Virus Vaccine DevelopmentR01AI152190 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI JUNG, JAE U · 2020 to 2024
$2.9M
Structural analysis and therapeutic nanobody development of KSHV G-protein coupled receptorR01CA251275 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI JUNG, JAE U · 2020 to 2024
$2.5M
KSHVmediated regulation of proline metabolismR01DE028521 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JUNG, JAE U · 2019 to 2023
$2.4M
KSHV-mediated metabolic reprogramming for LANA expression and viral persistencyR01AI181758 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI Jae U Jung · 2024 to 2026
$2.0M
HHS | National Institutes of Health (NIH) CA251275, CA294881, AI152190, AI17120, AI181758, DE023926, DE028521National Science and Technology Council (NSTC) 109-2926-I-010-503NCI NIH HHS R01 CA251275NCI NIH HHS U01 CA294881NIAID NIH HHS R01 AI152190NIAID NIH HHS R01 AI181758NIDCR NIH HHS R01 DE023926NIDCR NIH HHS R01 DE028521
6 · The paper itself

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV)/human herpesvirus 8 is an etiological agent of Kaposi's Sarcoma, multicentric Castleman's disease, and primary effusion lymphoma. Considering the high seroprevalence reaching up to 80% in sub-Saharan Africa, an effective vaccine is crucial for preventing KSHV infection. However, vaccine development has been limited due to the lack of an effective animal model that supports KSHV infection. Murine Herpesvirus 68 (MHV68), a natural mouse pathogen persisting lifelong post-infection, presents a promising model for KSHV infection. In this study, we developed KSHV vaccine and a chimeric MHV68 carrying the KSHV glycoprotein, serving as a surrogate challenge virus for testing KSHV vaccines in a mouse model. Among KSHV virion glycoproteins, K8.1 is the most abundant envelope glycoprotein with the highest immunogenicity. We developed two K8.1 vaccines: K8.1 mRNA-lipid nanoparticle (LNP) vaccine and K8.1

Indexed as

Antibodies, ViralHerpesvirus 8, HumanAnimalsDisease Models, AnimalFemaleHerpesviridae InfectionsHerpesvirus VaccinesHumansImmunogenicity, VaccineLiposomesMiceMice, Inbred C57BLNanoparticlesRhadinovirusSarcoma, KaposiVaccine DevelopmentAntibodies, ViralHerpesvirus VaccinesK8.1 protein, Human herpesvirus 8Lipid NanoparticlesLiposomesViral Envelope ProteinsViral ProteinsViral VaccinesKaposi's sarcoma-associated herpesvirusMHV68vaccines

Identifiers

PMID39475238
PMCPMC11633179

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.