Evidence map›Paper›PMID 37352115›Full record

ArticleeLife2023

Liver type 1 innate lymphoid cells lacking IL-7 receptor are a native killer cell subset fostered by parenchymal niches.

Takuma Asahi, Shinya Abe, Guangwei Cui, Akihiro Shimba, Tsukasa Nabekura, Hitoshi Miyachi, Satsuki Kitano, Keizo Ohira, Johannes M Dijkstra, Masaki Miyazaki and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Takuma AsahiLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.ORCID 0000-0001-6372-7563
Shinya AbeLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Guangwei CuiLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Akihiro ShimbaLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Tsukasa NabekuraLife Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Japan.
Hitoshi MiyachiReproductive Engineering Team, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Satsuki KitanoReproductive Engineering Team, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Keizo OhiraLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Johannes M DijkstraCenter for Medical Science, Fujita Health University, Aichi, Japan.ORCID 0000-0001-7097-3826
Masaki MiyazakiLaboratory of Immunology, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Akira ShibuyaLife Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Japan.ORCID 0000-0002-4480-4858
Hiroshi OhnoRIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Koichi IkutaLaboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.ORCID 0000-0003-1319-1021
Kyoto University · JPUniversity of Tsukuba · JPFujita Health University · JPRIKEN Center for Integrative Medical Sciences · JP

Funding

Japan Society for the Promotion of Science 19K16687Japan Society for the Promotion of Science 20H03501Japan Society for the Promotion of Science 20K21525Japan Society for the Promotion of Science 21K07067
6 · The paper itself

Abstract

Group 1 innate lymphoid cells (G1-ILCs), including circulating natural killer (NK) cells and tissue-resident type 1 ILCs (ILC1s), are innate immune sentinels critical for responses against infection and cancer. In contrast to relatively uniform NK cells through the body, diverse ILC1 subsets have been characterized across and within tissues in mice, but their developmental and functional heterogeneity remain unsolved. Here, using multimodal in vivo approaches including fate-mapping and targeting of the interleukin 15 (IL-15)-producing microenvironment, we demonstrate that liver parenchymal niches support the development of a cytotoxic ILC1 subset lacking IL-7 receptor (7 R

Indexed as

Interleukin-15LymphocytesAnimalsImmunity, InnateKiller Cells, NaturalLiverMiceReceptors, Interleukin-7Interleukin-15Receptors, Interleukin-7cytotoxicitydevelopmentILC1simmunologyinflammationInterleukin 15mousenicheNK cells

Identifiers

PMID37352115
PMCPMC10289810
OpenAlexW4381804149

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.