Evidence map›Paper›PMID 38974213›Full record

ReviewImmune network2024

Influenza Virus-Derived CD8 T Cell Epitopes: Implications for the Development of Universal Influenza Vaccines.

Sang-Hyun Kim, Erica Españo, Bill Thaddeus Padasas, Ju-Ho Son, Jihee Oh, Richard J Webby, Young-Ran Lee, Chan-Su Park, Jeong-Ki Kim

Abstract readReview
In one paragraph

Review in Immune network, 2024. 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
–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

11 citing papers in PubMed.

  1. Influenza.Nature reviews. Disease primers · 2026
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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.

Sang-Hyun KimDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0000-0002-7360-0491
Erica EspañoDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0000-0003-1437-9069
Bill Thaddeus PadasasDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0000-0002-9048-260X
Ju-Ho SonDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0009-0007-2513-5621
Jihee OhDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0009-0000-9032-1016
Richard J WebbyDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38195, USA.ORCID https://orcid.org/0000-0002-4397-7132
Young-Ran LeeBio-Convergence R&D Division, Korea Institute of Ceramic Engineering and Technology, Cheongju 28160, Korea.ORCID https://orcid.org/0000-0001-8696-5513
Chan-Su ParkDepartment of Pharmaceutics, College of Pharmacy, Chungbuk National University, Cheongju 28644, Korea.ORCID https://orcid.org/0000-0003-4968-8304
Jeong-Ki KimDepartment of Pharmacy, Korea University College of Pharmacy, Sejong 30019, Korea.ORCID https://orcid.org/0000-0003-1520-1377

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The influenza virus poses a global health burden. Currently, an annual vaccine is used to reduce influenza virus-associated morbidity and mortality. Most influenza vaccines have been developed to elicit neutralizing Abs against influenza virus. These Abs primarily target immunodominant epitopes derived from hemagglutinin (HA) or neuraminidase (NA) of the influenza virus incorporated in vaccines. However, HA and NA are highly variable proteins that are prone to antigenic changes, which can reduce vaccine efficacy. Therefore, it is essential to develop universal vaccines that target immunodominant epitopes derived from conserved regions of the influenza virus, enabling cross-protection among different virus variants. The internal proteins of the influenza virus serve as ideal targets for universal vaccines. These internal proteins are presented by MHC class I molecules on Ag-presenting cells, such as dendritic cells, and recognized by CD8 T cells, which elicit CD8 T cell responses, reducing the likelihood of disease and influenza viral spread by inducing virus-infected cell apoptosis. In this review, we highlight the importance of CD8 T cell-mediated immunity against influenza viruses and that of viral epitopes for developing CD8 T cell-based influenza vaccines.

Indexed as

Cytotoxic T lymphocytesInfluenza A virusInfluenza vaccinesT cell-based vaccinesT cell epitopes

Identifiers

PMID38974213
PMCPMC11224667

What OpenQuestion holds

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LicenceCC BY-NC
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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.