PATHOGENETIC JUSTIFICATION OF THE USE OF PROBIOTICS IN PREPARATION PROGRAMS FOR ASSISTED REPRODUCTIVE TECHNOLOGIES IN WOMEN WITH ENDOMETRIOSIS BASED ON STUDYING INDICATORS OF THE LEVEL OF MESOTHELIN, mRNA IL1β, HMGB1, NLRP3-INFLAMMASOME

In: Proceeding of the Shevchenko Scientific Society. Medical Sciences · 2024 · vol. 76(2) · doi:10.25040/ntsh2024.02.14 · W4406807584
article OA: diamond CC0
AI-generated summary by claude@2026-06, 2026-06-08

This study measured higher serum mesothelin, NLRP3, IL-1β, and HMGB1 mRNA expression in women with endometriosis-associated infertility, suggesting probiotics' potential in ART preparation.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-10 · read from full text

This paper studied 88 women with endometriosis-associated infertility and 68 women with tubal infertility to assess whether biomarkers linked to inflammation and mesothelin differed between groups, using serum and peritoneal fluid measurements plus RT-PCR for NLRP3 inflammasome gene expression (NLRP3, IL1β, HMGB1) and ELISA for mesothelin. It found significantly higher mesothelin levels in the endometriosis-associated group than controls, along with markedly elevated serum and peritoneal-fluid expression of NLRP3, IL-1β, and HMGB1, with primary infertility showing higher levels than secondary infertility. A key limitation noted by the study design is that it does not experimentally test probiotics during ART preparation; instead it frames probiotics as a pathogenetic rationale. Relevance to endometriosis: the entire study is focused on endometriosis-associated infertility and specifically evaluates NLRP3/IL1β/HMGB1 inflammation-related markers and mesothelin in that context to justify probiotic use in ART preparation.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Introduction. Treatment of infertility in women with endometriosis is an important and unsolved problem both in Ukraine and in the world. Along with this, in this cohort of patients, the efficiency of using assisted reproductive technologies (ART) remains low. The optimal approach in the program of preparation for ART of women with endometriosis is precisely probiotics with the content of lactobacilli as potential factors for reducing the production of provoking mediators of endometriosis and increasing the chances of a successful pregnancy. Aim: To justify the feasibility of including probiotics in the program of preparation for intrauterine reproductive technologies in women with endometriosis-associated infertility. Methods and materials. The study included 88 women with endometriosis associated with infertility (the main group) and 68 women with tubal infertility (the control group). To analyze the expression of the NLPP3-inflammasome gene, HMGB1, IL1β and determine the relative normalized expression of NLRP3, HMGB1, IL1β mRNA, we used the polymerase chain reaction with reverse transcription in real-time (RT-PCR). The mesothelin level in blood serum was determined using the solid-phase enzyme-linked immunosorbent assay (ELISA). Results. In earlier stages of the work, the levels of pro-inflammatory markers such as the peritoneal damage marker mesothelin and the expression of NLRP3, IL-1β and HMGB1 in serum and locally in the peritoneal fluid were investigated in women with endometriosis associated with infertility, and results were obtained indicating a probable increase all the indicators listed above. In particular, a significantly higher average level of mesothelin concentration in blood plasma was observed in the main group compared to the control group (0,73±0,01 ng/ml and 0,49±0,01 ng/ml) (p<0,05); NLRP3-inflammasome mRNA expression level (44,43±3,72 c.u. and 0,85±0,03 c.u.) (p˂0,001); IL1β mRNA gene expression (26,47±0,01 c.u. and 0,45±0,01 c.u.) (p˂0,001) and HMGB1 mRNA expression (11,91±0,01 c.u. and 1,00±0,01 c.u.) (р˂0,001). When evaluating these parameters depending on the nature of infertility (primary or secondary), results were also obtained, which indicate that women with endometriosis and primary infertility had significantly higher levels of mesothelin, NLRP3, IL-1β, and HMGB1 inflammasome activity. In particular, the level of mesothelin in women of the main group with primary infertility was significantly higher compared to women with secondary infertility both in blood serum and peritoneal fluid, respectively (0,86±0,001 ng/ml and 0,69±0,001 ng/ ml) (p<0,01) to (0,67±0,001 ng/ml and 0,42±0,001 ng/ml) (p<0,001). Conclusions. The study confirmed that the mRNA expression levels of NLRP3, IL-1β, HMGB1 and mesothelin correlate with the severity of endometriosis and can be potential markers of disease progression. These molecules are promising targets for further therapeutic strategies in the treatment of infertility-associated endometriosis. The study showed that the level of mesothelin in blood serum is 1,25 times higher in women with primary infertility than with secondary infertility and correlates with the severity of the disease, which indicates its possibility to be an independent marker for the diagnosis of endometriosis. The literature data indicates that the use of probiotics in programs of preparation for assisted reproductive technologies (ART) in women with endometriosis is appropriate.
Full text 11,810 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Methods

and materials. The study included 88 women with endometriosis associated with infertility (the main group) and 68 women with tubal infertility (the control group). To analyze the expression of the NLPP3-inflammasome gene, HMGB1, IL1β and determine the relative normalized expression of NLRP3, HMGB1, IL1β mRNA, we used the polymerase chain reaction with reverse transcription in real-time (RT-PCR). The mesothelin level in blood serum was determined using the solid-phase enzyme-linked immunosorbent assay (ELISA). Results. In earlier stages of the work, the levels of pro-inflammatory markers such as the peritoneal damage marker mesothelin and the expression of NLRP3, IL-1β and HMGB1 in serum and locally in the peritoneal fluid were investigated in women with endometriosis associated with infertility, and results were obtained indicating a probable increase all the indicators listed above. In particular, a significantly higher average level of mesothelin concentration in blood plasma was observed in the main group compared to the control group (0,73±0,01 ng/ml and 0,49±0,01 ng/ml) (p<0,05); NLRP3-inflammasome mRNA expression level (44,43±3,72 c.u. and 0,85±0,03 c.u.) (p˂0,001); IL1β mRNA gene expression (26,47±0,01 c.u. and 0,45±0,01 c.u.) (p˂0,001) and HMGB1 mRNA expression (11,91±0,01 c.u. and 1,00±0,01 c.u.) (р˂0,001). When evaluating these parameters depending on the nature of infertility (primary or secondary), results were also obtained, which indicate that women with endometriosis and primary infertility had significantly higher levels of mesothelin, NLRP3, IL-1β, and HMGB1 inflammasome activity. In particular, the level of mesothelin in women of the main group with primary infertility was significantly higher compared to women with secondary infertility both in blood serum and peritoneal fluid, respectively (0,86±0,001 ng/ml and 0,69±0,001 ng/ ml) (p<0,01) to (0,67±0,001 ng/ml and 0,42±0,001 ng/ml) (p<0,001). Conclusions. - The study confirmed that the mRNA expression levels of NLRP3, IL-1β, HMGB1 and mesothelin correlate with the severity of endometriosis and can be potential markers of disease progression. These molecules are promising targets for further therapeutic strategies in the treatment of infertility-associated endometriosis. - The study showed that the level of mesothelin in blood serum is 1,25 times higher in women with primary infertility than with secondary infertility and correlates with the severity of the disease, which indicates its possibility to be an independent marker for the diagnosis of endometriosis. - The literature data indicates that the use of probiotics in programs of preparation for assisted reproductive technologies (ART) in women with endometriosis is appropriate. Downloads

References

Endometriosis Associated Infertility: A Critical Review and Analysis on Etiopathogenesis and Therapeutic Approaches/ L.Filip et al.Medicina. 2020. Vol.56, no.9. P. 460. doi: https://doi.org/10.3390/medicina56090460 Endometriosis-Associated Infertility / E.-S. Nada et al. Medicina Moderna - Modern Medicine. 2018. Vol.25, no.3. P.131–136. doi: https://doi.org/10.31689/rmm.2018.25.3.131 Dunselman GA, Vermeulen N, Becker C, Calhaz-Jorge C, D'Hooghe T, De Bie B, et al. ESHRE guideline: management of women with endometriosis. Hum Reprod. 2014;29:400–12. doi: https://doi.org/10.1093/humrep/det457 Management of endometriosis-related infertility: Considerations and treatment options / D. Lee et al. Clinical and Experimental Reproductive Medicine. 2020. Vol. 47, no. 1. P.1–11. doi: https://doi.org/10.5653/cerm.2019.02971 Ata B., Telek SB Assisted reproductive technology for women with endometriosis, a clinically oriented review. Current Opinion in Obstetrics & Gynecology. 2021. Vol. 33, no. 3. P. 225–231. doi: https://doi.org/10.1097/gco.0000000000000710 Endometriosis and Assisted Reproductive Technology: A Review Article / A. Ajayi et al. Medical & Clinical Reviews. 2017. Vol.03, no.01. doi: https://doi.org/10.21767/2471-299x.1000046 Nanda AKT, Banerjee P., Dutta M., Wangdi T., Sharma P., Chaudhury K., Jana SK Cytokines, Angiogenesis, and Extracellular Matrix Degradation are Augmented by Oxidative Stress in Endometriosis. Ann. Lab. Med. 2020;40:390–397. doi: https://doi.org/10.3343/alm.2020.40.5.390 Hypothetical roadmap towards endometriosis: prenatal endocrine-disrupting chemical pollutant exposure, anogenital distance, gut-genital microbiota and subclinical infections / P. García-Peñarrubia et al. Human Reproduction Update. 2020. Vol. 26, no. 2. P. 214–246. doi: https://doi.org/10.1093/humupd/dmz044 Gruber TM, Mechsner S. Pathogenesis of Endometriosis: The Origin of Pain and Subfertility. Cells. 2021. Vol.10, no.6. P.1381. doi: https://doi.org/10.3390/cells10061381 Zheng D., Liwinski T., Elinav E. Interaction between microbiota and immunity in health and disease. Cell Research. 2020. Vol. 30, no. 6. P.492–506. doi: https://doi.org/10.1038/s41422-020-0332-7 Gut microbiota and systemic immunity in health and disease / BC Lo et al. International Immunology. 2020. doi: https://doi.org/10.1093/intimm/dxaa079 Punzón-Jiménez P., Labarta E. The impact of the female genital tract microbiome in women’s health and reproduction: a review. Journal of Assisted Reproduction and Genetics. 2021. doi: https://doi.org/10.1007/s10815-021-02247-5 Microbiota and Human Reproduction: The Case of Female Infertility / R. Tomaiuolo et al. High-Throughput. 2020. Vol.9, no.2. P.12. doi: https://doi.org/10.3390/ht9020012 Wee BA, Thomas M, Sweeney EL, Frentiu FD, Samios M, Ravel J, et al. A retrospective pilot study to determine whether the reproductive tract microbiota differs between women with a history of infertility and fertile women. Aust New Zeal J Obstet Gynaecol. 2018;58:341–348. doi: https://doi.org/10.1111/ajo.12754 The Vaginal Microbiome as a Tool to Predict rASRM Stage of Disease in Endometriosis: a Pilot Study / AR Perrotta et al. Reproductive Sciences. 2020. Vol. 27, no. 4. P.1064–1073. doi: https://doi.org/10.1007/s43032-019-00113-5 Schoenmakers S., Laven J. The vaginal microbiome as a tool to predict IVF success. Current Opinion in Obstetrics and Gynecology. 2020. Vol. 32, no. 3. P.169–178. doi: https://doi.org/10.1097/gco.0000000000000626 P–399 Temporal dynamics of an IVF/ICSI success prediction test based on the vaginal microbiome / A. Bielfeld et al. Human Reproduction. 2021. Vol. 36, Supplement_1. doi: https://doi.org/10.1093/humrep/deab130.398 García-Velasco JA, Budding D, Campe H, Malfertheiner SF, Hamamah S, Santjohanser C, et al. The reproductive microbiome – clinical practice recommendations for fertility specialists. Reprod BioMed Online. 2020;41:443–453. doi: https://doi.org/10.1016/j.rbmo.2020.06.014 Giordano G., Ferioli E., Tafuni A. The Role of Mesothelin Expression in Serous Ovarian Carcinoma: Impacts on Diagnosis, Prognosis, and Therapeutic Targets. Cancers. 2022. Vol. 14, no. 9. P. 2283. doi: https://doi.org/10.3390/cancers14092283 Epithelial-Mesenchymal Transition in Endometriosis–When Does It Happen? / L. Konrad et al. Journal of Clinical Medicine. 2020. Vol.9, no.6. P. 1915. doi: https://doi.org/10.3390/jcm9061915 Mesothelial cells regulate immune responses in health and disease: role for immunotherapy in malignant mesothelioma / SE Mutsaers et al. Current Opinion in Immunology. 2020. Vol. 64. P.88–109. doi: https://doi.org/10.1016/j.coi.2020.04.005 Mesothelin-targeted CAR-T cell therapy for solid tumors. Expert Opinion on Biological Therapy. 2020. P. 1–14. doi: https://doi.org/10.1080/14712598.2021.1843628 NLRP3 inflammasome-mediated Pyroptosis induces Notch signal activation in endometriosis angiogenesis / M. Zhang et al. Molecular and Cellular Endocrinology. 2023. P. 111952. doi: https://doi.org/10.1016/j.mce.2023.111952 Effectiveness of NLRP3 Inhibitor as a Non-Hormonal Treatment for ovarian endometriosis / M. Murakami et al. Reproductive Biology and Endocrinology. 2022. Vol. 20, no. 1. doi: https://doi.org/10.1186/s12958-022-00924-3 Potential of Lactobacillus acidophilus to modulate cytokine production by peripheral blood monocytes in patients with endometriosis / F. Mehdizadeh Sari et al. Iranian Journal of Microbiology. 2022. doi: https://doi.org/10.18502/ijm.v14i5.10965 Baker JM, Chase DM, Herbst-Kralovetz MM. Uterine Microbiota: residents, tourists, or invaders? Front Immunol. 2018;9:1–16. doi: https://doi.org/10.3389/fimmu.2018.00208 Moreno I, Franasiak JM. Endometrial microbiota — a new player in town. Fertil Steril. 2017;108:32–39. doi: https://doi.org/10.1016/j.fertnstert.2017.05.034 Schoenmakers S, Laven J. The vaginal microbiome as a tool to predict IVF success. Curr Opin Obstet Gynecol. 2020;32:169–178. doi: https://doi.org/10.1097/GCO.0000000000000626 García-Velasco JA, Budding D, Campe H, Malfertheiner SF, Hamamah S, Santjohanser C, et al. The reproductive microbiome – clinical practice recommendations for fertility specialists. Reprod BioMed Online. 2020;41:443–453. doi: https://doi.org/10.1016/j.rbmo.2020.06.014 Sepideh Khodaverdi, Robabeh Mohammadbeigi, Mojdeh Khaledi et al., Beneficial Effects of Oral Lactobacillus on Pain Severity in Women Suffering from Endometriosis: A Pilot Placebo-Controlled Randomized Clinical Trial. 2019 Oct;13(3):178-183. doi: https://doi.org/10.22074/ijfs.2019.5584 Franasiak JM, Werner MD, Juneau CR, Tao X, Landis J, Zhan Y, et al. Endometrial microbiome at the time of embryo transfer: next-generation sequencing of the 16S ribosomal subunit. J Assist Reprod Genet. 2016;33:129–136. doi: https://doi.org/10.1007/s10815-015-0614-z Uterine deficiency of high-mobility group box-1 (HMGB1) protein causes implantation defects and adverse pregnancy outcomes / S. Aikawa et al. Cell Death & Differentiation. 2019. Vol. 27, no. 5. P. 1489–1504. doi: https://doi.org/10.1038/s41418-019-0429-z Regulatory mechanisms of HMGB1 and its receptors in polycystic ovary syndrome-driven gravid uterine inflammation / M. Hu et al. The FEBS Journal. 2022. doi: https://doi.org/10.1111/febs.16678 Koval H, Chopiak V, Kamyshnyi A. mRNA tlr2 and tlr4 expression in the endometrium tissue in women with endometriosis associated with infertility. Georgian Med News. 2015 Jul-Aug;(244-245):7-11. PMID: 26177128. Harris HE, Andersson U, Pisetsky DS. HMGB1: a multifunctional alarmin driving autoimmune and inflammatory disease. Nat Rev Rheumatol. 2012;8:195–202. doi: https://doi.org/10.1038/nrrheum.2011.222 Deng M, Tang Y, Li W, Wang X, Zhang R, Zhang X, et al. The endotoxin delivery protein HMGB1 mediates caspase-11-dependent lethality in sepsis. Immunity. 2018;49:740–53 e7. doi: https://doi.org/10.1016/j.immuni.2018.08.016

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosisinfertility

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (33)

Source provenance

openalex
last seen: 2026-06-04T00:00:01.174412+00:00
License: CC0 · commercial use OK