Evidence map›Paper›PMID 29484187›Full record

ReviewClinical & translational immunology2018

Vaccinating for natural killer cell effector functions.

Helen R Wagstaffe, Jason P Mooney, Eleanor M Riley, Martin R Goodier

Open access · goldAbstract readReview
In one paragraph

Review in Clinical & translational immunology, 2018. 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
2.2field-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, 37 citations in OpenAlex.

  1. Article
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  10. Targeting natural killer cells to enhance vaccine responses.Trends in pharmacological sciences · 2021
    Review
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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.

Helen R WagstaffeDepartment of Immunology and Infection London School of Hygiene and Tropical Medicine London UK.ORCID 0000-0002-4462-7484
Jason P MooneyDepartment of Immunology and Infection London School of Hygiene and Tropical Medicine London UK.
Eleanor M RileyDepartment of Immunology and Infection London School of Hygiene and Tropical Medicine London UK.
Martin R GoodierDepartment of Immunology and Infection London School of Hygiene and Tropical Medicine London UK.ORCID 0000-0002-8963-4768
London School of Hygiene & Tropical Medicine · GBRoslin Institute · GB

Funding

Medical Research Council G1000808Medical Research Council MR/P000959/1
6 · The paper itself

Abstract

Vaccination has proved to be highly effective in reducing global mortality and eliminating infectious diseases. Building on this success will depend on the development of new and improved vaccines, new methods to determine efficacy and optimum dosing and new or refined adjuvant systems. NK cells are innate lymphoid cells that respond rapidly during primary infection but also have adaptive characteristics enabling them to integrate innate and acquired immune responses. NK cells are activated after vaccination against pathogens including influenza, yellow fever and tuberculosis, and their subsequent maturation, proliferation and effector function is dependent on myeloid accessory cell-derived cytokines such as IL-12, IL-18 and type I interferons. Activation of antigen-presenting cells by live attenuated or whole inactivated vaccines, or by the use of adjuvants, leads to enhanced and sustained NK cell activity, which in turn contributes to T cell recruitment and memory cell formation. This review explores the role of cytokine-activated NK cells as vaccine-induced effector cells and in recall responses and their potential contribution to vaccine and adjuvant development.

Indexed as

accessory cellcytokinesNK cellvaccination

Identifiers

PMID29484187
PMCPMC5822400
OpenAlexW2790173384

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.