A case of autosomal dominant polycystic kidney disease with systemic lupus erythematosus developing after SARS-CoV-2 vaccination
- PMID: 40392435
- DOI: 10.1007/s13730-025-00999-y
A case of autosomal dominant polycystic kidney disease with systemic lupus erythematosus developing after SARS-CoV-2 vaccination
Erratum in
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Correction: A case of autosomal dominant polycystic kidney disease with systemic lupus erythematosus developing after SARS‑CoV‑2 vaccination.CEN Case Rep. 2025 Jul 15. doi: 10.1007/s13730-025-01021-1. Online ahead of print. CEN Case Rep. 2025. PMID: 40659940 No abstract available.
Abstract
Although SARS-CoV-2 vaccines, particularly mRNA-based formulations, have demonstrated high efficacy and safety, adverse events including autoimmune activity have been reported. We report a case of systemic lupus erythematosus (SLE) following SARS-CoV-2 vaccination in a 52-year-old Japanese female with autosomal dominant polycystic kidney disease (ADPKD). The patient presented with nephrotic syndrome and severe thrombocytopenia and fulfilled the following four criteria for SLE classification: positive antinuclear antibodies, positive anti-ds-DNA antibodies, renal involvement, and reductions in two blood cell lines (leukopenia and thrombocytopenia). The patient responded favorably to prednisolone therapy, although hydroxychloroquine was avoided because of a suspected allergic predisposition. This case underscores the potential for exogenous triggers such as vaccination to induce SLE, highlighting the need for vigilance in managing autoimmune responses, particularly in patients with chronic conditions such as ADPKD. Despite the patient's history of ADPKD, no previous reports have linked this condition to post-vaccine SLE. Concurrent nephrotic syndrome in patients with ADPKD is rare, and the possibility of other treatable glomerular diseases should be considered when this is seen.
Keywords: Autosomal dominant polycystic kidney disease (ADPKD); Coronavirus disease 2019 (COVID-19); SARS-CoV-2 vaccination; Systemic lupus erythematosus (SLE).
© 2025. The Author(s).
Conflict of interest statement
Declarations. Conflict of interest: The authors declare no conflicts of interest. Ethical standards: This article does not contain any studies with human participants or animals performed by any of the authors. Consent for publication: Written informed consent to publish the case (concerning personal or clinical details to be published in this case report) was obtained from the patient.
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