Transitional Lesions, One More Step Towards Understanding the Pathogenesis of Adenomyosis
Emilie Wacheul1,2, Marie-Madeleine Dolmans1,3, Jérôme Ambroise4
1Gynecology Research Unit, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, 1200 Brussels, Belgium.
Journal of Clinical Medicine
|July 12, 2025
Summary
Mast cells are elevated in adenomyosis transitional lesions, suggesting their role in disease development and pain. Immune cell infiltrates were generally reduced in adenomyotic tissues, supporting the tissue injury and repair hypothesis.
Area of Science:
- Gynecology
- Immunology
- Pathology
Background:
- Adenomyosis is a benign gynecological disorder linked to abnormal uterine bleeding, dysmenorrhea, and subfertility.
- Its pathogenesis remains unclear, with the tissue injury and repair (TIAR) mechanism widely accepted.
- Immune system involvement is suspected but requires clarification due to inconsistent findings.
Purpose of the Study:
- To investigate immune cell phenotypes in adenomyotic uteri using a novel multiplex technique.
- To analyze immune cell distribution across different menstrual cycle phases in adenomyosis.
- To elucidate the role of immune cells in adenomyosis pathogenesis.
Main Methods:
- Immunohistochemistry and multiplex immunofluorescence were employed.
- Immune cell populations were analyzed in 30 adenomyotic and 15 healthy hysterectomy samples.
- Samples were evaluated based on menstrual cycle phase.
Main Results:
- Adenomyotic and transitional lesions showed reduced immune infiltrates (T cells, NK cells, B cells, macrophages, dendritic cells) compared to eutopic endometrium.
- Mast cells were significantly increased in transitional adenomyotic lesions.
- Transitional lesions indicated the progressive nature of adenomyosis.
Conclusions:
- Mast cells are implicated in adenomyosis development, pain, tissue remodeling, angiogenesis, and neurogenic inflammation.
- Findings support the TIAR hypothesis and highlight the progressive nature of adenomyosis.
- Further research into immune-targeted therapies for adenomyosis is warranted.
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