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Endometriotic tissue-derived exosomes downregulate NKg2D-mediated cytotoxicity and promote apoptosis : mechanisms for survival of ectopic endometrial tissue in endometriosis

Björk, Emma, 1977- (författare)
Umeå universitet,Obstetrik och gynekologi,Immunologi/immunkemi,Division of Obstetrics and Gynecology, Örnsköldsvik Hospital, Örnsköldsvik, Sweden
Israelsson, Pernilla (författare)
Umeå universitet,Institutionen för diagnostik och intervention,Onkologi
Nagaev, Ivan (författare)
Umeå universitet,Klinisk immunologi
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Nagaeva, Olga, 1958- (författare)
Umeå universitet,Klinisk immunologi
Lundin, Eva (författare)
Umeå universitet,Patologi
Ottander, Ulrika (författare)
Umeå universitet,Obstetrik och gynekologi
Mincheva-Nilsson, Lucia (författare)
Umeå universitet,Klinisk immunologi
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 (creator_code:org_t)
The American Association of Immunologists, 2024
2024
Engelska.
Ingår i: Journal of Immunology. - : The American Association of Immunologists. - 0022-1767 .- 1550-6606. ; 213:5, s. 567-576
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Endometriosis, affecting 10% of women, is defined as implantation, survival, and growth of endometrium-like/endometriotic tissue outside the uterine cavity, causing inflammation, infertility, pain, and susceptibility to ovarian cancer. Despite extensive studies, its etiology and pathogenesis are poorly understood and largely unknown. The prevailing view is that the immune system of endometriosis patients fails to clear ectopically disseminated endometrium from retrograde menstruation. Exosomes are small extracellular vesicles that exhibit immunomodulatory properties. We studied the role of endometriotic tissue-secreted exosomes in the pathophysiology of endometriosis. Two exosome-mediated mechanisms known to impair the immune response were investigated: 1) downregulation of NKG2D-mediated cytotoxicity and 2) FasL- and TRAIL-induced apoptosis of activated immune cells. We showed that secreted endometriotic exosomes isolated from supernatants of short-term explant cultures carry the NKG2D ligands MICA/B and ULBP1-3 and the proapoptotic molecules FasL and TRAIL on their surface, i.e., signature molecules of exosome-mediated immune suppression. Acting as decoys, these exosomes downregulate the NKG2D receptor, impair NKG2D-mediated cytotoxicity, and induce apoptosis of activated PBMCs and Jurkat cells through the FasL- and TRAIL pathway. The secreted endometriotic exosomes create an immunosuppressive gradient at the ectopic site, forming a “protective shield” around the endometriotic lesions. This gradient guards the endometriotic lesions against clearance by a cytotoxic attack and creates immunologic privilege by induction of apoptosis in activated immune cells. Taken together, our results provide a plausible, exosome-based mechanistic explanation for the immune dysfunction and the compromised immune surveillance in endometriosis and contribute novel insights into the pathogenesis of this enigmatic disease.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

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