Evidence map›Paper›PMID 26257169›Full record

ArticleCell reports2015

Metabolic Damage and Premature Thymus Aging Caused by Stromal Catalase Deficiency.

Ann V Griffith, Thomas Venables, Jianjun Shi, Andrew Farr, Holly van Remmen, Luke Szweda, Mohammad Fallahi, Peter Rabinovitch, Howard T Petrie

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
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  9. Article
  10. Article
  11. Age-Related Thymic Involution.Advances in experimental medicine and biology · 2025
    Review
  12. Article
  13. Targeting catalase in cancer.Redox biology · 2024
    Review
  14. Review
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  16. Review
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  19. Article
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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

9 authors at 3 institutions in 1 country.

Ann V GriffithDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA.
Thomas VenablesDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA.
Jianjun ShiDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA.
Andrew FarrDepartments of Biological Structure and Immunology, The University of Washington, South Lake Union E-411, 750 Republican Street, Box 358059, Seattle, WA 98109, USA.
Holly van RemmenFree Radical Biology and Aging Research Program, The Oklahoma Medical Research Foundation, MS 21, 825 NE 13(th) Street, Oklahoma City, OK 73104, USA.
Luke SzwedaFree Radical Biology and Aging Research Program, The Oklahoma Medical Research Foundation, MS 21, 825 NE 13(th) Street, Oklahoma City, OK 73104, USA.
Mohammad FallahiDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA.
Peter RabinovitchDepartment of Pathology, The University of Washington, 1959 NE Pacific Avenue, HSB K-081, Box 357705, Seattle, WA 98195, USA.
Howard T PetrieDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA. Electronic address: htpetrie@scripps.edu.
Scripps Research Institute · USOklahoma Medical Research Foundation · USUniversity of Washington · US

Funding

Identification of stromal responses during castration-induced thymic regrowth.R01AG031576 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI PETRIE, HOWARD T. · 2009 to 2014
$2.0M
Stromal catalase deficiency as the causative factor in accelerated thymic atrophyR01AI103340 · NIAID · SCRIPPS FLORIDA · PI PETRIE, HOWARD T. · 2013 to 2016
$1.9M
Visualizing epithelial network connectivity in thymus biology, aging, and regenerationR01AI130303 · NIAID · SCRIPPS FLORIDA · PI CAI, DAWEN, PETRIE, HOWARD T. · 2017 to 2019
$1.4M
BLRD VA I01 BX002595NIAID NIH HHS AI103340NIAID NIH HHS R01 AI103340NIA NIH HHS AG031576NIA NIH HHS R01 AG031576
6 · The paper itself

Abstract

T lymphocytes are essential mediators of immunity that are produced by the thymus in proportion to its size. The thymus atrophies rapidly with age, resulting in progressive diminution of new T cell production. This decreased output is compensated by duplication of existing T cells, but it results in gradual dominance by memory T cells and decreased ability to respond to new pathogens or vaccines. Here, we show that accelerated and irreversible thymic atrophy results from stromal deficiency in the reducing enzyme catalase, leading to increased damage by hydrogen peroxide generated by aerobic metabolism. Genetic complementation of catalase in stromal cells diminished atrophy, as did chemical antioxidants, thus providing a mechanistic link between antioxidants, metabolism, and normal immune function. We propose that irreversible thymic atrophy represents a conventional aging process that is accelerated by stromal catalase deficiency in the context of an intensely anabolic (lymphoid) environment.

Indexed as

Aging, PrematureAnimalsCatalaseHumansHydrogen PeroxideMiceMice, Inbred C57BLMitochondriaThymus GlandT-LymphocytesCatalaseHydrogen Peroxide

Identifiers

PMID26257169
PMCPMC4797338
OpenAlexW1708735479

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.