Study on the relationship between CXCR3 and its ligands and tubal tuberculosis

Life Sci. 2021 May 1:272:119047. doi: 10.1016/j.lfs.2021.119047. Epub 2021 Jan 14.

Abstract

Objective: Chemokines play an important role in Mycobacterium tuberculosis infection. We aimed to investigate CXCR3, CXCL9, CXCL10 and CXCL11 to explore the correlation between the severity of tubal tuberculosis and chemokines.

Methods: 26 patients with tubal tuberculosis diagnosed in our hospital from 2016 to 2019 were selected as the experimental group, and 18 female patients who underwent high-risk pregnancy supervision in our hospital from 2016 to 2018 were selected as the control group. The pathological manifestations of tubal tuberculosis were observed by HE staining, the expressions of CXCR3 and its ligands in fallopian tubes were detected by immunohistochemistry.

Results: Typical granulomatous structure of tubal tuberculosis was observed by HE staining and most of them were accompanied by massive necrosis in the experimental group, while no granulomatous lesions were found in the control group. The results of immunohistochemical staining showed that CXCR3 and its ligands were expressed in the cytoplasm and nucleus of oviduct epithelial cells and inflammatory cells, in the granuloma area. CXCL9, CXCL10 and CXCL11 were related to the severity of the disease.

Key findings: CXCR3 and its ligands were positively expressed in tubal tuberculosis, especially CXCL9, CXCL10 and CXCL11 were positively correlated with the severity of fallopian tube disease.

Significance: It is helpful for clinical diagnosis and treatment detection, and provides a new therapeutic target for the study of female genital tuberculosis in the future.

Keywords: CXCL10; CXCL11; CXCL9; CXCR3; Tubal tuberculosis.

MeSH terms

  • Adult
  • Chemokine CXCL10 / metabolism
  • Chemokine CXCL11 / metabolism
  • Chemokine CXCL9 / metabolism
  • Chemokines
  • China
  • Epithelial Cells / metabolism
  • Fallopian Tubes / microbiology*
  • Fallopian Tubes / pathology
  • Female
  • Granuloma / metabolism
  • Humans
  • Ligands
  • Middle Aged
  • Receptors, CXCR3 / metabolism*
  • Receptors, CXCR3 / physiology
  • Tuberculosis / metabolism
  • Tuberculosis, Female Genital / metabolism*
  • Tuberculosis, Female Genital / physiopathology

Substances

  • CXCL10 protein, human
  • CXCL11 protein, human
  • CXCL9 protein, human
  • CXCR3 protein, human
  • Chemokine CXCL10
  • Chemokine CXCL11
  • Chemokine CXCL9
  • Chemokines
  • Ligands
  • Receptors, CXCR3