Evidence map›Paper›PMID 20220095›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

NK cells influence both innate and adaptive immune responses after mucosal immunization with antigen and mucosal adjuvant.

Lindsay J Hall, Simon Clare, Gordon Dougan

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Lindsay J HallWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom. l.hall@ucc.ie
Simon Clare
Gordon Dougan
Wellcome Sanger Institute · GB

Funding

Wellcome Trust 076962
6 · The paper itself

Abstract

NK cells were found to be recruited in a temporally controlled manner to the nasal-associated lymphoid tissue and the cervical lymph nodes of mice after intranasal immunization with Ag85B-early secreted antigenic target 6 kDa from Mycobacterium tuberculosis mixed with Escherichia coli heat-labile toxin as adjuvant. These NK cells were activated and secreted a diverse range of cytokines and other immunomodulators. Using Ab depletion targeting anti-asialo GM1, we found evidence for altered trafficking, impaired activation, and cytokine secretion of dendritic cells, macrophages, and neutrophils in immunized NK cell-depleted mice compared with control animals. Analysis of Ag-specific immune responses revealed an attenuated Ab and cytokine response in immunized NK cell-depleted animals. Systemic administration of rIL-6 but not rIFN-gamma significantly restored immune responses in mice depleted of NK cells. In conclusion, cytokine production, particularly IL-6, via NK cells and NK cell-activated immune populations plays an important role in the establishment of local innate immune responses and the consequent development of adaptive immunity after mucosal immunization.

Indexed as

Adaptive ImmunityImmunity, InnateAcyltransferasesAdjuvants, ImmunologicAdministration, IntranasalAnimalsAntigens, BacterialBacterial ProteinsFemaleG(M1) GangliosideImmunoglobulin GInterleukin-6Killer Cells, NaturalLymphocyte DepletionMiceMice, Inbred BALB CAcyltransferasesAdjuvants, Immunologicantigen 85B, Mycobacterium tuberculosisAntigens, Bacterialasialo GM1 gangliosideBacterial ProteinsESAT-6 protein, Mycobacterium tuberculosisG(M1) GangliosideImmunoglobulin GInterleukin-6

Identifiers

PMID20220095
PMCPMC3517975
OpenAlexW2104188180

What OpenQuestion holds

Textmetadata
LicenceTDM
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.