Increased frequency of human leukocyte antigen-E inhibitory receptor CD94/NKG2A-expressing peritoneal natural killer cells in patients with endometriosis
- PMID: 17706207
- DOI: 10.1016/j.fertnstert.2007.05.018
Increased frequency of human leukocyte antigen-E inhibitory receptor CD94/NKG2A-expressing peritoneal natural killer cells in patients with endometriosis
Abstract
Objective: To analyze the frequency of peritoneal natural killer (NK) cells expressing the human leukocyte antigen (HLA)-E receptor CD94/NKG2A in patients with endometriosis.
Design: Case-control study.
Setting: University hospital.
Patient(s): Stage III and stage IV endometriosis, according to the revised American Society for Reproductive Medicine classification, was laparoscopically and histologically confirmed in 11 and 9 patients, respectively; 13 subjects without endometriosis were selected for the control group.
Intervention(s): Collection of peripheral venous blood, peritoneal fluid, endometriotic tissue, and normal endometrium in subjects undergoing laparoscopy.
Main outcome measure(s): Surface expression levels of CD94/NKG2A and CD94/NKG2C were detected by three-color cytofluorometric analysis. Semiquantitative HLA-E messenger RNA expression analysis was performed in endometriotic lesions and in eutopic endometrium. NK cell-mediated cytotoxic activity toward HLA-E positive target, DT360 cell line, was also determined.
Result(s): In women with endometriosis, the percentage of CD94/NKG2A-positive peritoneal NK cells was significantly higher than in the control group. The CD94/NKG2A ligand, HLA-E, was detected at high levels in endometriotic tissue as messenger RNA transcript. Target cells bearing HLA-E were resistant to NK cell-mediated lysis in a CD94/NKG2A-dependent manner.
Conclusion(s): Increased expression of CD94/NKG2A in peritoneal NK cells may mediate the resistance of endometriotic tissue to NK cell-mediated lysis, thus contributing to the progression of the disease.
Similar articles
-
HLA-E binds to natural killer cell receptors CD94/NKG2A, B and C.Nature. 1998 Feb 19;391(6669):795-9. doi: 10.1038/35869. Nature. 1998. PMID: 9486650
-
Association of CD94/NKG2A, CD94/NKG2C, and its ligand HLA-E polymorphisms with Behcet's disease.Tissue Antigens. 2007 Oct;70(4):307-13. doi: 10.1111/j.1399-0039.2007.00907.x. Tissue Antigens. 2007. PMID: 17767552
-
HLA-G recognition by human natural killer cells. Involvement of CD94 both as inhibitory and as activating receptor complex.Eur J Immunol. 1997 Aug;27(8):1875-80. doi: 10.1002/eji.1830270809. Eur J Immunol. 1997. PMID: 9295021
-
The cell biology of the human natural killer cell CD94/NKG2A inhibitory receptor.Mol Immunol. 2005 Feb;42(4):485-8. doi: 10.1016/j.molimm.2004.07.031. Mol Immunol. 2005. PMID: 15607803 Review.
-
[CD94/NKG2A--a kind of inhibitory receptor belonging to C-type lectin superfamily].Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002 Dec;24(6):653-5. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002. PMID: 12905700 Review. Chinese.
Cited by
-
A higher number of exhausted local PD1+, but not TIM3+, NK cells in advanced endometriosis.Heliyon. 2023 Dec 10;10(1):e23294. doi: 10.1016/j.heliyon.2023.e23294. eCollection 2024 Jan 15. Heliyon. 2023. PMID: 38173487 Free PMC article.
-
Efficacy of N-Acetylcysteine on Endometriosis-Related Pain, Size Reduction of Ovarian Endometriomas, and Fertility Outcomes.Int J Environ Res Public Health. 2023 Mar 7;20(6):4686. doi: 10.3390/ijerph20064686. Int J Environ Res Public Health. 2023. PMID: 36981595 Free PMC article.
-
Single-Cell RNA Sequencing of PBMCs Identified Junction Plakoglobin (JUP) as Stratification Biomarker for Endometriosis.Int J Mol Sci. 2024 Dec 5;25(23):13071. doi: 10.3390/ijms252313071. Int J Mol Sci. 2024. PMID: 39684780 Free PMC article.
-
Endometriosis in Adolescents: A Closer Look at the Pain Characteristics and Atypical Symptoms: A Prospective Cohort Study.J Clin Med. 2025 Feb 19;14(4):1392. doi: 10.3390/jcm14041392. J Clin Med. 2025. PMID: 40004922 Free PMC article.
-
Endometriosis: A Disease with Few Direct Treatment Options.Molecules. 2022 Jun 23;27(13):4034. doi: 10.3390/molecules27134034. Molecules. 2022. PMID: 35807280 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials