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Updated: Jan 20, 2026

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Interleukin-17 receptor C gene polymorphism reduces treatment effect and promotes poor prognosis of ischemic stroke
Jing Tian1, Yongjie Bai2, Aimin You3
1Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan Province, China.
Insights
Ischemic stroke (IS) is linked to increased Interleukin-17 receptor C (IL-17RC) gene expression and specific polymorphisms. The IL-17RC re37511 variant is associated with poorer treatment outcomes and prognosis in IS patients.
Area of Science:
- Genetics and Molecular Biology
- Neurology
- Immunology
Background:
- Interleukin-17 receptor C (IL-17RC) plays a role in inflammatory responses.
- Gene polymorphisms can influence susceptibility and outcomes in various diseases.
- Ischemic stroke (IS) is a significant global health concern with complex underlying mechanisms.
Purpose of the Study:
- To investigate the association between Interleukin-17 receptor C (IL-17RC) gene polymorphism and ischemic stroke (IS).
- To evaluate the correlation between IL-17RC gene variants and clinical outcomes in IS patients.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and Western blotting were used to measure mRNA and protein levels of IL-17 and IL-17RC.
- Polymerase chain reaction (PCR) amplification was employed for IL-17RC genotyping.
- Case-control study involving 300 IS patients and 300 healthy controls.
Main Results:
- Elevated mRNA and protein levels of IL-17 and IL-17RC were observed in IS patients compared to controls.
- A significantly higher proportion of the IL-17RC re37511 polymorphism was found in the IS group.
- The IL-17RC re37511 variant was associated with poorer treatment effects, higher mortality, and recurrence rates.
Conclusions:
- Ischemic stroke is associated with upregulated IL-17 and IL-17RC expression.
- The IL-17RC re37511 polymorphism serves as a potential indicator of poor prognosis and treatment response in IS.
Objective:
To study the relationship between Interleukin-17 receptor C (IL-17RC) gene polymorphism and ischemic stroke (IS).
Methods:
Three hundred cases of IS patients and 300 cases of the healthy controls were selected. Serum of IS patients and the controls was collected. The relative mRNA levels of IL-17, IL-17RC, IL-6, IL-8, G-CSF and granulocyte-macrophage colony stimulating factor (GM-CSF) by qRT-PCR. The protein expression of IL-17 and IL-17RC was determined by Western blotting. IL-17RC genotype was identified by PCR amplification. The proportion of IL-17RC, SNP and re37511 in IS and control group was determined. The treatment effect on IS and prognosis of patients with IL-17RC, SNP and re37511 was compared.
Results:
The relative mRNA levels of IL-17, IL-17RC, IL-6, IL-8, G-CSF and GM-CSF in IS group were significantly higher than the control group. The protein expression of IL-17 and IL-17RC in IS group was also markedly higher than the control group. The proportion of IL-17RC re37511 in IS group was much larger than control group and proportion of IL-17RC much less. The percent of poor treatment effect in re37511 was much larger than IL-17RC. The percent of death and recrudescence in patients with IL-17RC re37511 was the highest.
Conclusion:
IS up-regulates the expression of IL-17 and IL-17RC. IL-17RC re37511 indicates the patients have a poorer treatment effect and prognosis.
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