Evidence map›Paper›PMID 41929480›Full record

Observational studyFrontiers in immunology2026

Impact of testosterone-based gender-affirming hormone therapy on toll-like receptor transcript levels and peripheral blood leukocyte counts in transmasculine individuals.

Hüseyin Cihan, Özge Güngör, Gökcen Ünal Kocabas, Esma Pehlivan Köroglu, Kübra Gülpinar, Erhan Pariltay, Ömür Ardeniz, Guy T'Sjoen, Jonatan Leffler, Bettina Winzeler and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

11 authors.

Hüseyin CihanFaculty of Medicine, Zurich University, Zurich, Switzerland.
Özge GüngörDepartment of Medical Genetics, Ege University Hospital, Izmir, Türkiye.
Gökcen Ünal KocabasDepartment of Endocrinology, Ege University Hospital, Izmir, Türkiye.
Esma Pehlivan KörogluDepartment of Endocrinology, Ege University Hospital, Izmir, Türkiye.
Kübra GülpinarDepartment of Endocrinology, Ege University Hospital, Izmir, Türkiye.
Erhan PariltayDepartment of Medical Genetics, Ege University Hospital, Izmir, Türkiye.
Ömür ArdenizDepartment of Allergy and Immunology, Ege University Hospital, Izmir, Türkiye.
Guy T'SjoenDepartment of Endocrinology, Ghent University Hospital, Ghent, Belgium.
Jonatan LefflerThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Bettina WinzelerZurich University Hospital, Zurich, Switzerland.
Banu Sarer YürekliDepartment of Endocrinology, Ege University Hospital, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sex differences in immune responses are partly attributed to sex hormones, with testosterone generally associated with dampened immune responses. However, the specific impact of testosterone on the innate immune system in humans remains unclear. We examined changes in toll-like receptor (TLR) transcript levels and peripheral blood leukocyte parameters during masculinizing hormone therapy in transmasculine individuals. Methods: We conducted a 6-month prospective observational study in 20 transmasculine individuals initiating testosterone-based gender-affirming hormone therapy. Peripheral blood mononuclear cells were collected at baseline and after 6 months of therapy. Gene transcript levels of TLR1-8, TLR10, MD2, and CD14 were quantified by RT-qPCR. Serum hormones and hematologic parameters were measured by standard assays. Results: After 6 months of testosterone therapy, serum testosterone levels rose to values comparable to the range in cisgender men. Lymphocyte and monocyte counts increased ( Conclusions: In this cohort, testosterone-based gender-affirming hormone therapy is associated with the upregulation of TLR8 and TLR10 transcripts, suggesting that sex hormone shifts (increased testosterone and decreased estradiol) may modulate certain innate immune receptors at the transcript level. These findings provide insights into how gender-affirming hormone therapy can influence the innate immune system in transmasculine individuals.

Indexed as

TestosteroneToll-Like ReceptorsTransgender PersonsAdultFemaleHumansImmunity, InnateLeukocyte CountMaleProspective StudiesRNA, MessengerYoung AdultRNA, MessengerTestosteroneToll-Like ReceptorsGAHTleukocytetestosteroneTLRstransgendertransmasculine

Identifiers

PMID41929480
PMCPMC13038929

What Socratic 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 Socratic graph.