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Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Antiphospholipid Syndrome and the Kidney
Savino Sciascia1, Simone Baldovino2, Karen Schreiber3
1Center of Research of Immunopathology and Rare Diseases, Department of Clinical and Biological Sciences, University of Turin, Turin, Italy; Louise Coote Lupus Unit, Guy's and St Thomas' National Health Service (NHS) Foundation Trust, St Thomas' Hospital, London, UK.
Antiphospholipid syndrome (APS) involves blood clots and pregnancy issues, often linked with lupus. Understanding antiphospholipid antibodies (aPL) is key for managing kidney complications in these patients.
Area of Science:
- Rheumatology
- Nephrology
- Immunology
Background:
- Antiphospholipid syndrome (APS) is an autoimmune disorder causing thrombosis and pregnancy complications.
- APS can be primary or secondary to other autoimmune diseases, notably systemic lupus erythematosus (SLE).
- A significant overlap exists between SLE and APS, with 40% of SLE patients having antiphospholipid antibodies (aPL).
Purpose of the Study:
- To review renal manifestations in SLE patients with aPL.
- To discuss the impact of aPL on kidney disease in SLE.
- To highlight the importance of differentiating inflammatory from thrombotic kidney lesions.
Main Methods:
- Literature review of renal manifestations in APS and SLE.
- Analysis of the role of aPL in lupus nephritis.
- Discussion of aPL's impact on end-stage renal disease and pregnancy in SLE.
Main Results:
- APS is characterized by thrombosis, pregnancy morbidity, and aPL.
- SLE patients with aPL face specific renal challenges.
- Distinguishing thrombotic from inflammatory kidney damage is vital for treatment.
Conclusions:
- Renal involvement in SLE patients with aPL requires careful evaluation.
- aPL significantly influences the course of lupus nephritis and other renal outcomes.
- Therapeutic strategies must consider both autoimmune and thrombotic aspects.
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