Evidence map›Paper›PMID 12452827›Full record

ArticleClinical and experimental immunology2002

Characteristics of immunity induced by viral antigen or conferred by antibody via different administration routes.

T Matsuoka, Y Okamoto, Z Matsuzaki, S Endo, E Ito, H Tsutsumi, R A Williamson, H Sakurai, D R Burton, I Saito

Open access · greenAbstract readComparative Study
In one paragraph

Article in Clinical and experimental immunology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

T MatsuokaDepartment of Otolaryngology, Yamanashi Medical University, Japan.
Y Okamoto
Z Matsuzaki
S Endo
E Ito
H Tsutsumi
R A Williamson
H Sakurai
D R Burton
I Saito
Scripps Research Institute · USUniversity of Yamanashi · JPAkita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The characteristics of the immunity induced by viral antigens or conferred by antiviral antibody via different routes of administration were evaluated comparatively. C57BL/6 mice were immunized via intranasal, intradermal or enteric routes with a live recombinant vaccinia virus expressing the respiratory syncytial virus (RSV) F glycoprotein (F.rVV) or RSV, and then challenged intranasally with RSV. Inhibition of RSV replication was observed in the lungs of all the mice; however, only intranasal immunization hindered virus replication in the nose. Lung inflammation, characterized by infiltration of neutrophils and of mononuclear cells was strongest in the intradermally immunized mice, but was observed in all F.rVV immunized mice to various degrees. Intranasal administration of a potently neutralizing human anti-RSV antibody Fab fragment to infected mice inhibited RSV replication in the nose and, when combined with intraperitoneal administration, protected both the lung and the nose in the absence of deleterious lung pathology. These data suggest that intranasal immunization with F.rVV reduces RSV replication in the respiratory tract, but still induces pathological lung inflammation, even though this is milder than that observed following intradermal immunization. Local neutralizing antibody is indispensable for protection in the nose.

Indexed as

Administration, CutaneousAdministration, IntranasalAnimalsAntibodies, ViralAntigens, ViralHumansImmunoglobulin Fab FragmentsInjections, IntraperitonealLungMaleMiceMice, Inbred C57BLRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsViral Fusion ProteinsVirus ReplicationAntibodies, ViralAntigens, ViralImmunoglobulin Fab FragmentsViral Fusion Proteins

Identifiers

PMID12452827
PMCPMC1906556
OpenAlexW2041732844

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.