The Serum Level of CXCL9, CXCL10, and CXCL11 and the Expression of CXCR3 of Peripheral Blood Mononuclear Cells in Brucellosis Patients

被引:2
作者
Hassanshahi, Farzaneh [1 ]
Karimabad, Mojgan Noroozi [2 ]
Miranzadeh, Elahe [1 ]
Hassanshahi, Gholamhossein [2 ]
Torabizadeh, Seyedeh Atekeh [3 ]
Jebali, Ali [2 ]
机构
[1] Islamic Azad Univ, Fac Vet Med, Shahr Ekord Branch, Shahr Ekord, Iran
[2] Rafsanjan Univ Med Sci, Res Inst Basic Med Sci, Mol Med Res Ctr, Rafsanjan, Iran
[3] Kerman Univ Med Sci, Inst Neuropharmacol, Pharmaceut Res Ctr, Kerman, Iran
关键词
GENETIC-VARIATION; INTERFERON-GAMMA; EPITHELIAL-CELLS; BETA-DEFENSINS; T-CELLS; CCL20; CHEMOKINES; INNATE; TISSUE; CCR6;
D O I
10.1007/s00284-023-03230-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Brucella spp. can replicate in human endothelial cells, inducing an inflammatory response with increased expression of chemokines. Although Brucella infects humans, its ability to induce the production of chemokines by lung cells is unknown. Therefore, the current investigation was designed to examine the association between brucellosis and CXCL9, 10, and 11 chemokines. The patient group included 71 patients suffering from Brucella infection and the control group consisted of 50 healthy ranchers from the same geographical area. Serum levels of CXCL9, CXCL10, and CXCL11 were analyzed by ELISA. The fold changes of CXCR3 expression against beta-actin were determined by real-time-PCR technique. Western blotting analysis was also applied for evaluating the expression of CXCR3 at protein level. The results of this study showed that the serum levels of CXCL9, CXCL10, and CXCL11 are significantly increased in acute brucellosis patients in comparison to control as indicated by ELISA test, mRNA levels of CXCR3 by Real-time PCR as well as protein levels of CXCR3 by Western blot analysis. According to findings, these chemokines have the potential to serve as markers for brucellosis patients. Taken together, cytokine/chemokine network was active in acute brucellosis patients, and it is suggested to evaluate other cytokines in future studies.
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