Evidence map›Paper›PMID 36548468›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Restored Thymic Output after Androgen Blockade Participates in Antitumor Immunity.

Fanny Polesso, Breanna Caruso, Scott A Hammond, Amy E Moran

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Sex Steroid Hormone Regulation of T-Cell Function and Antitumor Immunity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Thymic regeneration and tumor immunotherapy.Frontiers in immunology · 2026
    Review
  9. Review
  10. Age-Related Thymic Involution.Advances in experimental medicine and biology · 2025
    Review
  11. Article
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 3 countries.

Fanny PolessoCell, Developmental and Cancer Biology, Oregon Health and Science University, Portland, OR.
Breanna CarusoCell, Developmental and Cancer Biology, Oregon Health and Science University, Portland, OR.ORCID 0000-0001-6163-1023
Scott A HammondDiscovery Biosciences, R&D Oncology, AstraZeneca, Gaithersburg, MD; and.ORCID 0000-0001-5800-4328
Amy E MoranCell, Developmental and Cancer Biology, Oregon Health and Science University, Portland, OR.ORCID 0000-0003-1952-7737
Oregon Health & Science University · USAstraZeneca (Netherlands) · NL

Funding

Understanding how T cell intrinsic androgen receptor activity influences cell differentiation and dysfunctionR37CA263592 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Amy E Moran · 2021 to 2026
$3.2M
NCI NIH HHS R37 CA263592
6 · The paper itself

Abstract

The thymus is a hormone-sensitive organ, which involutes with age in response to production of sex steroids. Thymic involution leads to a decrease in the generation of recent thymic emigrants (RTEs), resulting in a reduced response to immune challenges such as cancer. Interestingly, the standard of care for prostate cancer patients is androgen deprivation therapy (ADT), which leads to thymic regeneration and an increase in thymic output. It remains unknown whether these newly produced T cells can contribute to the antitumor immune response. This study defines the kinetics of thymic regeneration in response to ADT in mice, determining that thymic epithelial cell proliferation is critical for the increase in RTE output. Using a mouse model to track RTE in vivo, we demonstrate that these newly generated RTEs can traffic to tumors, where they become activated and produce effector cytokines at levels similar to more mature T cells. Collectively, these data suggest that RTEs produced from ADT-induced thymic regeneration could be harnessed for the antitumor immune response.

Indexed as

Prostatic NeoplasmsThymus GlandAndrogen AntagonistsAndrogensHumansMaleT-LymphocytesAndrogen AntagonistsAndrogens

Identifiers

PMID36548468
PMCPMC9898132
OpenAlexW4312112954

What OpenQuestion holds

Textmetadata
LicenceTDM
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.