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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
A case of lupus nephritis flare-up in severe COVID-19 infection
A S Yusuf1, X K Cheong2, M Rozita3
1Universiti Kebangsaan Malaysia Medical Centre, Faculty of Medicine, Department of Internal Medicine, Nephrology Unit, Kuala Lumpur, Malaysia. mdyusuf@ppukm.ukm.edu.my.
Insights
This case study shows that treating severe COVID-19 in lupus nephritis patients with immunosuppressants two weeks after illness onset is safe. Kidney function stabilized, demonstrating a viable treatment approach for immune-mediated glomerulonephritis during viral infection.
Area of Science:
- Nephrology
- Infectious Diseases
- Rheumatology
Background:
- COVID-19 poses significant risks, especially for patients with comorbidities like lupus nephritis (LN).
- Management of severe COVID-19 often involves supportive care, antivirals, and immunosuppressants.
- Lupus nephritis flares can cause acute kidney injury (AKI), complicating COVID-19 treatment.
Observation:
- A patient with lupus nephritis presented with severe COVID-19 and an LN flare with AKI.
- Initial treatment included Favipiravir, low-dose methylprednisolone, and hydroxychloroquine.
- Despite initial recovery from COVID-19, the patient had a prolonged positive RT-PCR swab (29 days) and persistent proteinuria.
Findings:
- High-dose intravenous methylprednisolone was administered two weeks after illness onset, despite persistent viral shedding.
- The patient's condition improved, and kidney function stabilized with ongoing proteinuria.
- This approach suggests safety in using high-dose immunosuppressants in recovered COVID-19 patients.
Implications:
- This case provides evidence for managing COVID-19 in patients with active immune-mediated glomerulonephritis.
- It suggests that high-dose immunosuppressive therapy can be safely initiated two weeks post-illness in selected recovered COVID-19 patients.
- This approach may offer a therapeutic option for patients with concurrent severe infections and autoimmune kidney diseases.
Abstract:
The novel Coronavirus disease 2019 (COVID-19) had rapidly spread and became a worldwide pandemic since its detection in Wuhan, China. The disease has caused significant morbidity and mortality, particularly among patients with comorbidities. The current treatment involves supportive management alongside antiviral therapy and immunosuppressant therapy in severely affected patients. We describe a case of a patient with underlying lupus nephritis (LN) who presented with severe COVID-19 infection and concomitant LN flare with acute kidney injury (AKI). The patient was treated with antiviral therapy, Favipiravir, considering his risk of developing severe COVID-19 infection. As the patients would usually have AKI alongside LN flare, we administered initial steroid therapy at a lower dose (Methylprednisolone 50mg daily) and oral hydroxychloroquine despite the initial concerns on immunosuppressant usage in COVID-19 infections. Although our patient recovered relatively well from COVID- 19 infection, he continued to have positive reverse transcriptase-polymerase chain reaction (RT-PCR) nasopharyngeal swab for COVID-19 up to 29 days of illness. His kidney function stabilised despite having persistent nephrotic range proteinuria. Hence, the attending team decided to pulse the patient with a high dose steroid (IV Methylprednisolone 250mg OD for three days) after two weeks of illness despite the persistent positive swab. The patient's condition continued to improve, and this case illustrates an approach in treating COVID-19 with concomitant active immune-mediated glomerulonephritis. We find that it is safe to institute high dose immunosuppressant in recovered COVID-19 patients two weeks after the illness.
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