Immunological parameters in patients with chronic opisthorchiasis coupled to mutant genes associated with predisposition to arterial hypertension development
- Authors: Grigorieva S.A.1, Stepanova K.B.1, Stepanova T.F.1, Ozerova A.N.1, Bakshtanovskaya I.V.1, Kalgina G.A.1, Kurlaeva L.V.1
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Affiliations:
- Tyumen Region Infection Pathology Research Institute
- Issue: Vol 15, No 1 (2025)
- Pages: 71-78
- Section: ORIGINAL ARTICLES
- URL: https://journals.rcsi.science/2220-7619/article/view/292130
- DOI: https://doi.org/10.15789/2220-7619-IPI-17711
- ID: 292130
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Abstract
To identify the features of immune system functioning in patients with chronic opisthorchiasis coupled to mutant gene loci associated with arterial hypertension predisposition, comprehensive studies on innate and adaptive immunity were conducted. The state of neutrophil engulfment and bactericidal activity was assessed. The phenotype of lymphocytes was determined by flow cytometry. The humoral arm of the immune system was assessed by quantitating total immunoglobulins of classes M, G, A and E. Gene polymorphisms were detected by pyrosequencing. The predisposition to arterial hypertension development was assessed by assessing polymorphisms in the gene loci: ARDB2 rs1042713; AGT rs4762; AGT rs699; AGTR1 rs5186; NOS3 rs1799983. In patients with chronic opisthorchiasis with and without polymorphisms AGT rs4762 and AGTR1 rs5186, had no difference in immune response. Patients with vs. without ARDB2 rs1042713 had suppressed humoral (reduced total IgE) along with activated innate immune response in chronic opisthorchiasis (increased absolute count of leukocytes and monocytes). In the group with the rare AGT rs699 vs. common allele there was a decrease in the percentage of lymphocytes, a lower total IgM level and increased percentage of B lymphocytes. Immune indicators in patients with chronic opisthorchiasis with vs. without rs1799983 mutation in the NOS3 gene had higher neutrophil bactericidal potential (stimulated nitrosine tetrazolium test (NST test)) along with percentage of T-helper cells (CD4+).
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##article.viewOnOriginalSite##About the authors
Svetlana A. Grigorieva
Tyumen Region Infection Pathology Research Institute
Author for correspondence.
Email: info@Tniikip.rospotrebnadzor.ru
Researcher, Clinical and Experimental Immunology Group
Russian Federation, TyumenK. B. Stepanova
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
PhD (Medicine), Associate Professor, Director
Russian Federation, TyumenT. F. Stepanova
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
DSc (Medicine), Professor, Head Researcher
Russian Federation, TyumenA. N. Ozerova
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
Researcher, Molecular Genetic and Parasitological Research Group
Russian Federation, TyumenI. V. Bakshtanovskaya
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
PhD (Biology), Head of the Molecular Genetic and Parasitological Research Group, Scientific Secretary
Russian Federation, TyumenG. A. Kalgina
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
PhD (Biology), Leading Researcher, Head of the Clinical and Experimental Immunology Group
Russian Federation, TyumenL. V. Kurlaeva
Tyumen Region Infection Pathology Research Institute
Email: info@Tniikip.rospotrebnadzor.ru
Junior Researcher, Clinical and Experimental Immunology Group
Russian Federation, TyumenReferences
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