| Literature DB >> 34524642 |
Keiko Wakabayashi1, Satoko Yamamoto2, Shigeo Hara3, Momoko Okawara2, Kumie Teramoto2, Natsuko Ikeda2, Yasuo Kusunoki2, Masanobu Takeji4.
Abstract
Immune check point inhibitors (ICIs) are now increasingly used for cancer therapy. At the same time, by activating the immune system, ICIs induce unique side effects, termed immune-related adverse events (irAEs). Renal irAEs, although uncommon, result in acute tubulointerstitial nephritis. Recently, because of an increase in ICI administration, renal irAEs, including glomerulonephritis, are being increasingly reported. A 69-year-old man presented with nephrotic syndrome after use of the ICI nivolumab. He underwent renal biopsy and was diagnosed with membranous nephropathy (MN) without acute tubulointerstitial nephritis. Immunofluorescence staining was negative for IgG4 and phospholipase A2 receptor (PLA2R), suggesting a malignancy-associated pattern. Oral glucocorticoid therapy was started as the standard treatment for irAEs, which resulted in complete remission of the nephrotic syndrome in 20 months. We suggest his MN was induced or accelerated by immune activation due to nivolumab. It means that ICIs possibly induce not only acute tubulointerstitial nephritis but also nephrotic syndrome due to MN as renal irAEs which is treatable with glucocorticoid.Entities:
Keywords: IgG subclass; Immune check point inhibitors (ICIs); Immune-related adverse events (irAEs); Membranous nephropathy (MN); Nephrotic syndrome; Nivolumab; Phospholipase A2 receptor (PLA2R)
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Year: 2021 PMID: 34524642 PMCID: PMC9061917 DOI: 10.1007/s13730-021-00645-3
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449