Evidence map›Paper›PMID 29860261›Full record

ReviewJournal of innate immunity2018

Mucosal Immune Response in Nasal-Associated Lymphoid Tissue upon Intranasal Administration by Adjuvants.

Hiromi Takaki, Shingo Ichimiya, Misako Matsumoto, Tsukasa Seya

Open access · goldAbstract readReview
In one paragraph

Review in Journal of innate immunity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Journal of microbiology and biotechnology · 2025
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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

4 authors at 2 institutions in 1 country.

Hiromi TakakiDepartment of Vaccine Immunology, Graduate School of Medicine, Hokkaido University, Sapporo, Japantakaki@sapmed.ac.jp.
Shingo IchimiyaDepartment of Human Immunology, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan.
Misako MatsumotoDepartment of Vaccine Immunology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Tsukasa SeyaDepartment of Vaccine Immunology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Hokkaido University · JPSapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nasal administration of vaccines directed against diseases caused by upper respiratory tract infections of pathogens, such as the influenza virus, mimics the natural infection of pathogens and induces immunoglobulin A (IgA) production in the nasal cavity to effectively protect viral entry. Therefore, the development of a nasally administered vaccine is a research objective. Because the antigenicity of influenza split vaccines is low, nasal inoculation with the vaccine alone does not induce strong IgA production in the nasal cavity. However, the addition of adjuvants activates the innate immune response, enhancing antigen-specific IgA production and the T-cell response. Although the development of suitable adjuvants for nasal vaccinations is in progress, the mechanism by which adjuvants promote the immune response is still unclear. In this review, we discuss the mucosal immune response, especially in the nasal-associated lymphoid tissue, induced in response to the intranasal inoculation of an influenza vaccine and adjuvants in animal models.

Indexed as

Adjuvants, ImmunologicAdministration, IntranasalAnimalsAntibodies, NeutralizingHumansImmunity, HumoralImmunity, MucosalInfluenza A virusInfluenza, HumanInfluenza VaccinesLymphoid TissueNasal MucosaOrthomyxoviridae InfectionsRespiratory Tract InfectionsT-LymphocytesAdjuvants, ImmunologicAntibodies, NeutralizingInfluenza VaccinesImmunoglobulin AInfluenza vaccineMucosal immunityNasal-associated lymphoid tissue

Identifiers

PMID29860261
PMCPMC6784108
OpenAlexW2807188525

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.