Evidence map›Paper›PMID 25876176›Full record

ReviewHuman vaccines & immunotherapeutics2015

Progress on adenovirus-vectored universal influenza vaccines.

Kui Xiang, Guan Ying, Zhou Yan, Yan Shanshan, Zhang Lei, Li Hongjun, Sun Maosheng

Open access · bronzeAbstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Construction and application of adenoviral vectors.Molecular therapy. Nucleic acids · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. SARS-CoV-2 vaccine candidates in rapid development.Human vaccines & immunotherapeutics · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 at 3 institutions in 3 countries.

Kui Xianga Department of Molecular Biology; Institute of Medical Biology; Chinese Academy of Medical Sciences; Peking Union Medical College ; Kunming , Yunnan , PR China.
Guan Ying
Zhou Yan
Yan Shanshan
Zhang Lei
Li Hongjun
Sun Maosheng
Academy of Medical Sciences · GBInstitute of Medical Biology · SGChina Tobacco · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza virus (IFV) infection causes serious health problems and heavy financial burdens each year worldwide. The classical inactivated influenza virus vaccine (IIVV) and live attenuated influenza vaccine (LAIV) must be updated regularly to match the new strains that evolve due to antigenic drift and antigenic shift. However, with the discovery of broadly neutralizing antibodies that recognize conserved antigens, and the CD8(+) T cell responses targeting viral internal proteins nucleoprotein (NP), matrix protein 1 (M1) and polymerase basic 1 (PB1), it is possible to develop a universal influenza vaccine based on the conserved hemagglutinin (HA) stem, NP, and matrix proteins. Recombinant adenovirus (rAd) is an ideal influenza vaccine vector because it has an ideal stability and safety profile, induces balanced humoral and cell-mediated immune responses due to activation of innate immunity, provides 'self-adjuvanting' activity, can mimic natural IFV infection, and confers seamless protection against mucosal pathogens. Moreover, this vector can be developed as a low-cost, rapid-response vaccine that can be quickly manufactured. Therefore, an adenovirus vector encoding conserved influenza antigens holds promise in the development of a universal influenza vaccine. This review will summarize the progress in adenovirus-vectored universal flu vaccines and discuss future novel approaches.

Indexed as

Drug CarriersGenetic VectorsAdenoviridaeAnimalsDrug DiscoveryHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza VaccinesNucleocapsid ProteinsOrthomyxoviridaeRNA-Binding ProteinsVaccines, SyntheticViral Core ProteinsViral Matrix ProteinsDrug CarriersHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesNP protein, Influenza A virusNucleocapsid Proteinsnucleoprotein, influenza B virusRNA-Binding ProteinsVaccines, SyntheticViral Core ProteinsViral Matrix ProteinsAd: adenovirusADCC, antibody-dependent cell-mediated cytotoxicityadenovirus vectorAPC, antigen-presenting cellbroadly neutralizing antibodiesCAR, Coxsackie-Adenovirus Receptorcellular immunityCTLs, cytotoxic T lymphocytesDC, lung dendritic cellsDVD, drug–vaccine duoFcγRs, Fc receptors for IgGflu, influenzaHA, hemagglutininHDAd, helper-dependent adenoviralHEK293, human embryonic kidney 293 cellhemagglutininHI, hemagglutination inhibitionHLA, human leukocyte antigenhumoral immunityIFV, Influenza virusIF-γ, interferon-γIIVV, inactivated influenza virus vaccineIL-2, interleukin-2influenzaITRs, inverted terminal repeatsLAIV, live attenuated influenza vaccineM1, matrix protein 1M2, matrix protein 2mAbs, monoclonal antibodiesMHC-I, major histocompatibility complex class Imucosal immunityNA, neuraminidaseNP, nucleoproteinrAd, recombinant adenovirusRCA, replication competent adenovirusuniversal vaccineVAERD, vaccine-associated enhanced respiratory disease

Identifiers

PMID25876176
PMCPMC4514376
OpenAlexW1847838282

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.