Publications by authors named "Dan Inoue"

Article Synopsis
  • The innate immune system plays a key role in acute kidney injury (AKI), but its specific involvement in sepsis-associated AKI (SA-AKI) in humans is still not fully understood.
  • A study analyzed 19 SA-AKI patients undergoing continuous renal replacement therapy, focusing on their serum cytokines, complement components, and innate immune cell types and functions.
  • Findings showed that while certain immune cell proportions were similar to healthy individuals, CD56 T cells exhibited increased FasL expression and a higher percentage of perforin-positive cells, indicating their active role in SA-AKI, along with significantly reduced immune functions of monocytes.
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A Japanese man in his early 70s was referred to our hospital because of massive proteinuria. Analysis of his kidney biopsy demonstrated glomerular subepithelial immune deposits containing immunoglobulin (Ig)G, which was dominant for the IgG1 subclass. Immunoperoxidase staining for neural epidermal growth factor-like 1 protein (NELL1) was positive on the glomerular capillary walls, whereas neither serum anti-phospholipase A2 receptor (PLAR) antibodies nor immunofluorescence staining for PLAR was positive.

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Proliferative glomerulonephritis with monoclonal immunoglobulin (Ig) G deposits (PGNMID) is a relatively uncommon entity of monoclonal gammopathy of renal significance, and its detailed pathogenesis is not well understood. We, herein, report two cases of patients with PGNMID; their renal biopsy showed glomerular histological features of membranoproliferative glomerulonephritis pattern with endocapillary proliferation accompanied by non-organized granular electron-dense deposits that consisted of monoclonal IgG3-lambda. Neither symptomatic episodes of preceding infection nor infection foci were found in both patients; however, glomerular positive staining for nephritis-associated plasmin receptor (NAPlr) and related plasmin activity were observed.

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Background: Anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (AAGN) is the fulminant glomerular diseases with poor renal prognosis. Activation of the complement system has recently been reported in the pathogenesis of AAGN, but it remains to be clarified as to which complement pathway is mainly involved.

Methods: 20 patients with myeloperoxidase (MPO)-AAGN were retrospectively evaluated.

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Background: To date, a few case reports have described the association between poststreptococcal acute glomerulonephritis (PSAGN) and hemolytic anemia/thrombocytopenia, both with or without a pathology similar to that of thrombotic microangiopathy (TMA). However, the detailed mechanism leading to the complication of TMA in PSAGN patients remains to be clarified. In contrast, infection with neuraminidase-producing Streptococcus pneumoniae is a well-known cause of TMA, and it has been reported that transient positivity of the direct Coombs test is observed in up to 90% of such patients.

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Background: Long-term peritoneal dialysis results in functional and histopathological alterations of the peritoneal membrane, leading to peritoneal fibrosis (PF). The mechanism of PF has not been fully elucidated, and at present there is no effective therapy for PF. Epimorphin is a mesenchymal protein that not only regulates morphogenesis in organ development but is implicated in tissue repair.

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Article Synopsis
  • A 74-year-old woman developed acute kidney injury (AKI) due to an infection with Capnocytophaga, a type of bacteria that produces neuraminidase.
  • A renal biopsy indicated tubulointerstitial damage and suggested the presence of Thomsen-Friedenreich antigen on tubular cells, possibly due to the neuraminidase's effect.
  • This case highlights a potential mechanism for AKI linked to Capnocytophaga infections, pointing to the need for more research on its causes and related damage.
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We report a case of pure red cell aplasia (PRCA) caused by parvovirus B19 (PVB19) infection, which was transmitted through a kidney allograft. The patient underwent a living-donor kidney transplant from his wife at the age of 60. Despite successful engraftment with a normal creatinine level, he developed severe anemia that required frequent blood transfusions 2 months after transplantation.

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We report a case of allergic acute tubulointerstitial nephritis (TIN) induced by acetaminophen in a 48-year-old Japanese man with no past medical history. Two days after receiving the non-steroidal anti-inflammatory drug (NSAID) loxoprofen for left shoulder pain, he developed cold symptoms such as fever and sore throat. He then took a 300 mg dose of acetaminophen three times a day and a 100 mg dose of minocycline hydrochloride twice a day for 7 days.

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