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Updated: May 16, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
[Correlation between CTLA-4 gene polymorphism and systemic lupus erythematosus: a meta-analysis]
Shui-lian Chen1, Fei Deng, Feng Jiang
1Department of Epidemiology, School of Public Health, Key Laboratory of Public Health Safety, Ministry of Education, Fudan University, Shanghai 200032, China.
Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) gene polymorphisms at -1722 and -318 loci are linked to systemic lupus erythematosus (SLE) susceptibility, particularly in Asian populations. Further research is warranted to explore these genetic associations.
Area of Science:
- Genetics
- Immunology
- Rheumatology
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease with a significant genetic component.
- The role of specific gene polymorphisms in SLE susceptibility requires further elucidation.
Purpose of the Study:
- To investigate the association between Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) gene polymorphisms and the risk of developing SLE.
- To analyze the correlation across different populations.
Main Methods:
- A comprehensive meta-analysis was conducted on 12 published studies.
- Searches were performed across major scientific databases (PubMed, Web of Knowledge, Embase, etc.) up to May 20, 2012.
- Data from three CTLA-4 gene loci (-1722, -1661, -318) were analyzed.
Main Results:
- Significant associations were found between CTLA-4 gene polymorphisms at the -1722 locus (dominant model) and -318 locus (recessive model) and SLE risk.
- These associations were particularly evident in the Asian population.
- No significant correlation was observed in European or African populations.
Conclusions:
- The CTLA-4 gene polymorphisms at the -1722T/C and -318T/C loci are associated with an increased susceptibility to SLE.
- The findings highlight a significant role for these specific CTLA-4 polymorphisms in SLE pathogenesis, especially within Asian ethnic groups.
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