Evidence map›Paper›PMID 27738345›Full record

ReviewOncotarget2017

Friend or foe: the dichotomous impact of T cells on neuro-de/re-generation during aging.

Brandon Coder, Weikan Wang, Liefeng Wang, Zhongdao Wu, Qichuan Zhuge, Dong-Ming Su

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. T cell aging and Alzheimer's disease.Frontiers in immunology · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Conditional Silencing of H-2DJournal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  10. Review
  11. Review
  12. Article
  13. Potential immunotherapies for traumatic brain and spinal cord injury.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2018
    Review
  14. Extracellular vesicles extracted from young donor serum attenuate inflammaging via partially rejuvenating aged T-cell immunotolerance.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  15. Review
  16. 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

6 authors at 4 institutions in 2 countries.

Brandon CoderInstitute of Molecular Medicine, University of North Texas Health Science Center, Fort Worth, TX, USA.
Weikan WangInstitute of Molecular Medicine, University of North Texas Health Science Center, Fort Worth, TX, USA.
Liefeng WangInstitute of Molecular Medicine, University of North Texas Health Science Center, Fort Worth, TX, USA.
Zhongdao WuZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, P. R. China.
Qichuan ZhugeZhejiang Provincial Key Laboratory of Aging and Neurological Disease Research, First Affiliated Hospital, Wenzhou Medical University, Wenzhou City, Zhejiang, P. R. China.
Dong-Ming SuInstitute of Molecular Medicine, University of North Texas Health Science Center, Fort Worth, TX, USA.
University of North Texas Health Science Center · USFirst Affiliated Hospital of Wenzhou Medical University · CNUniversity of North Texas · USWenzhou Medical University · CN

Funding

Training in the Neurobiology of Aging and Alzheimer's DiseaseT32AG020494 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI ROBERT Clinton BARBER, NATHALIE SUMIEN · 2002 to 2026
$6.9M
Balance of Thymic Negative Selection vs. Treg Cell Generation in the ElderlyR01AI121147 · NIAID · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI SU, DONG-MING · 2016 to 2020
$1.7M
NIAID NIH HHS R01 AI121147NIA NIH HHS T32 AG020494
6 · The paper itself

Abstract

The interaction between T cells and the central nervous system (CNS) in homeostasis and injury has been recognized being both pathogenic (CD4+ T-helper 1 - Th1, Th17 and γδT) and ameliorative (Th2 and regulatory T cells - Tregs). However, in-depth studies aimed to elucidate the precise in the aged microenvironment and the dichotomous role of Tregs have just begun and many aspects remain unclear. This is due, not only to a mutual dependency and reciprocal causation of alterations and diseases between the nervous and T cell immune systems, but also to an inconsistent aging of the two systems, which dynamically changes with CNS injury/recovery and/or aging process. Cellular immune system aging, particularly immunosenescence and T cell aging initiated by thymic involution - sources of chronic inflammation in the elderly (termed inflammaging), potentially induces an acceleration of brain aging and memory loss. In turn, aging of the brain via neuro-endocrine-immune network drives total body systemic aging, including that of the immune system. Therefore, immunotherapeutics including vaccination and "protective autoimmunity" provide promising means to rejuvenate neuro-inflammatory disorders and repair CNS acute injury and chronic neuro-degeneration. We review the current understanding and recent discoveries linking the aging immune system with CNS injury and neuro-degeneration. Additionally, we discuss potential recovery and rejuvenation strategies, focusing on targeting the aging T cell immune system in an effort to alleviate acute brain injury and chronic neuro-degeneration during aging, via the "thymus-inflammaging-neurodegeneration axis".

Indexed as

AgingCellular SenescenceCentral Nervous SystemHumansTh17 CellsTh1 CellsT-LymphocytesT-Lymphocytes, RegulatoryagingimmunotherapyneurodegenerationT-cell immunity

Identifiers

PMID27738345
PMCPMC5351694
OpenAlexW2530540379

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.