Evidence map›Paper›PMID 30068650›Full record

ArticleJournal of virology2018

Complement C3 Plays a Key Role in Inducing Humoral and Cellular Immune Responses to Influenza Virus Strain-Specific Hemagglutinin-Based or Cross-Protective M2 Extracellular Domain-Based Vaccination.

Yu-Jin Kim, Ki-Hye Kim, Eun-Ju Ko, Min-Chul Kim, Yu-Na Lee, Yu-Jin Jung, Young-Tae Lee, Young-Man Kwon, Jae-Min Song, Sang-Moo Kang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  18. The Quest for a Truly Universal Influenza Vaccine.Frontiers in cellular and infection microbiology · 2019
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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

10 authors at 4 institutions in 2 countries.

Yu-Jin KimInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Ki-Hye KimInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Eun-Ju KoInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Min-Chul KimInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Yu-Na LeeInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Yu-Jin JungInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Young-Tae LeeInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Young-Man KwonInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Jae-Min SongDepartment of Global Medical Science, Sungshin Women's University, Seoul, Republic of Korea.
Sang-Moo KangInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA skang24@gsu.edu.
Georgia State University · USAnimal and Plant Quarantine Agency · KRNational Institutes of Health · USSungshin Women's University · KR

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
LAIV Inducing Cross ProtectionR21AI119366 · NIAID · GEORGIA STATE UNIVERSITY · PI KANG, SANG-MOO · 2015 to 2016
$415k
NIAID NIH HHS R01 AI093772NIAID NIH HHS R01 AI105170NIAID NIH HHS R21 AI119366
6 · The paper itself

Abstract

The complement pathway is involved in eliminating antigen immune complexes. However, the role of the C3 complement system remains largely unknown in influenza virus M2 extracellular (M2e) domain or hemagglutinin (HA) vaccine-mediated protection after vaccination. Using a C3 knockout (C3 KO) mouse model, we found that complement protein C3 was required for effective induction of immune responses to vaccination with M2e-based or HA-based vaccines, which include isotype class-switched antibodies and effector CD4 and CD8 T cell responses. C3 KO mice after active immunization with cross-protective nonneutralizing M2e-based vaccine were not protected against influenza virus, although low levels of M2e-specific antibodies were protective after passive coadministration with virus in wild-type mice. In contrast, C3 KO mice that were immunized with strain-specific neutralizing HA-based vaccine were protected against homologous virus challenge despite lower levels of HA antibody responses. C3 KO mice showed impaired maintenance of innate immune cells and a defect in innate immune responses upon exposure to antigens. The findings in this study suggest that C3 is required for effective induction of humoral and cellular adaptive immune responses as well as protective immunity after nonneutralizing influenza M2e vaccination.

Indexed as

Immunity, CellularImmunity, HeterologousImmunity, HumoralAnimalsAntibodies, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesComplement C3Cross ProtectionHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesMice, Inbred C57BLMice, KnockoutViral Matrix ProteinsViroporin ProteinsAntibodies, ViralComplement C3Hemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesM2 protein, Influenza A virusViral Matrix ProteinsViroporin ProteinsCD4+ T cellsCD8+ T cellscomplementinfluenza vaccineinfluenza virusisotype-switched IgG antibodiesM2e5x VLPM2e virus-like particles

Identifiers

PMID30068650
PMCPMC6158440
OpenAlexW2886084202

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.