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The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice
Published on: November 1, 2015
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Towards Precision Medicine in Systemic Lupus Erythematosus
Elliott Lever1, Marta R Alves2, David A Isenberg1
1Centre for Rheumatology, Division of Medicine, University College Hospital London, London, UK.
Pharmacogenomics and Personalized Medicine
|February 27, 2020
Summary
Systemic lupus erythematosus (SLE) presents diverse clinical and immunological features. Precision medicine is challenging due to varying organ-specific immune abnormalities in SLE patients, delaying personalized treatment approaches.
Area of Science:
- Immunology
- Rheumatology
- Genetics
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease.
- SLE is characterized by diverse clinical manifestations and immunological dysregulation.
- Current treatments for SLE include steroids, immunosuppressives, and hydroxychloroquine, often used broadly across patient groups.
Purpose of the Study:
- To review the major immunological changes involved in SLE pathophysiology.
- To discuss the challenges in applying precision medicine to SLE.
- To explore the potential for future personalized treatment strategies in SLE.
Main Methods:
- This is a review article.
- The review synthesizes current literature on SLE immunology and pathophysiology.
- It discusses the implications of immunological diversity for treatment.
Main Results:
- SLE exhibits significant heterogeneity in its immunological abnormalities.
- These diverse immunopathological profiles vary across different organs and systems affected by the disease.
- The broad application of similar drugs may not be optimal for all SLE patients.
Conclusions:
- The heterogeneity of SLE pathophysiology presents a significant hurdle for implementing precision medicine.
- Tailoring treatments based on precise immunopathological profiles will require further research.
- Achieving true precision medicine in SLE is a long-term goal.

