Evidence map›Paper›PMID 27965471›Full record

ArticleOncotarget2017

Critical role of SP thymocyte motility in regulation of thymic output in neonatal Aire-/- mice.

Rong Jin, Abudureyimujiang Aili, Yuqing Wang, Jia Wu, Xiuyuan Sun, Yu Zhang, Qing Ge

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. 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 22% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Aire controls the recirculation of murine Foxp3European journal of immunology · 2018
    Article
  7. Article
  8. Twenty Years of AIRE.Frontiers in immunology · 2018
    Review
  9. Review
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

7 authors at 1 institution in 1 country.

Rong JinDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Abudureyimujiang AiliDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Yuqing WangDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Jia WuDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Xiuyuan SunDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Yu ZhangDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Qing GeDepartment of Immunology, Key Laboratory of Medical Immunology, Ministry of Health. Peking University Health Science Center, Beijing, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune regulator (Aire) is essential in the perinatal period to prevent the multiorgan autoimmunity. Here we show that Aire-regulated single positive thymocyte trafficking in neonatal period is critical for thymic egress. Reduced thymic emigration was found in Aire-/- mice during neonatal period, leading to enhanced homeostatic expansion of peripheral T cells as early as 2 weeks of age. In neonatal Aire-/- mice, thymic expression of CCR7 ligands were dramatically reduced, resulting in decreased thymocyte motility and thymocyte emigration. This reduction of thymic egress in Aire-/- mice was alleviated beyond 3 weeks of age by an early upregulation of S1P1 signaling. As the numbers and quality of thymic emigrants are essential for the establishment and maintenance of peripheral tolerance, the reduced thymic emigration during neonatal period may deteriorate autoimmunity caused by the emigration of autoreactive T cells.

Indexed as

AIRE ProteinAnimalsAnimals, NewbornAntigens, CDBiomarkersCell MovementHomeostasisLymphocyte ActivationLymphocyte CountMiceMice, KnockoutPhenotypeReceptors, CCR4Receptors, CCR7Receptors, LysosphingolipidThymocytesAIRE ProteinAntigens, CDBiomarkersReceptors, CCR4Receptors, CCR7Receptors, LysosphingolipidTranscription FactorsAire deficiencyCCR7Immune responseImmunityImmunology and Microbiology Sectionneonatal thymic emigrationthymocyte motility

Identifiers

PMID27965471
PMCPMC5352200
OpenAlexW2566271333

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.