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Review
. 2024 Jun 6;25(11):6266.
doi: 10.3390/ijms25116266.

Immune Checkpoints in Endometriosis-A New Insight in the Pathogenesis

Affiliations
Review

Immune Checkpoints in Endometriosis-A New Insight in the Pathogenesis

Dorota Suszczyk et al. Int J Mol Sci. .

Abstract

Endometriosis (EMS) is an oestrogen-dependent, chronic disease affecting women of a reproductive age. One of the important factors involved in the development of this disease is the complex disorders associated with the functioning of the immune system. Recent evidence has shown that EMS development is associated with changes in systemic and local immunity, including functional disturbances of effector and antigen-presenting cells. One of the reasons for immune imbalance can be the improper expression of immune checkpoints (ICPs). ICPs and their ligands are responsible for maintaining self-tolerance and the modulation of the initiation, duration, and magnitude of the immune response of effector cells in normal tissues to avoid tissue damage. Considering the complex nature of co-stimulatory or co-inhibitory ICPs and the signalling between effector cells and APCs, we hypothesise that changes in cells' activity caused by ICPs may lead to serious immune system disturbances in patients with endometriosis. Moreover, both upregulation and downregulation in the expression of ICPs may be implicated in this process, including the reduced activity of effector cells against endometrial implants and disturbances in the antigen-presenting process. In this narrative review, we discuss, for the first time, key findings from the emerging literature, describing the associations between ICPs and their possible implication in the pathogenesis of endometriosis.

Keywords: endometriosis; immune cells; immune checkpoints; immunosuppression.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
The possible role of ICPs in the pathogenesis and progression of endometriosis.
Figure 2
Figure 2
The future perspectives of ICPs in the pathogenesis of endometriosis.

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