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Bowman’s capsule provides a protective niche for podocytes from cytotoxic CD8+ T cells
Anqun Chen, Kyung Lee, Vivette D. D’Agati, Chengguo Wei, Jia Fu, Tian-Jun Guan, John Cijiang He, Detlef Schlondorff, Judith Agudo
Anqun Chen, Kyung Lee, Vivette D. D’Agati, Chengguo Wei, Jia Fu, Tian-Jun Guan, John Cijiang He, Detlef Schlondorff, Judith Agudo
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Concise Communication Immunology Nephrology

Bowman’s capsule provides a protective niche for podocytes from cytotoxic CD8+ T cells

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Abstract

T cells play a key role in immune-mediated glomerulonephritis, but how cytotoxic T cells interact with podocytes remains unclear. To address this, we injected EGFP-specific CD8+ T cells from just EGFP death inducing (Jedi) mice into transgenic mice with podocyte-specific expression of EGFP. In healthy mice, Jedi T cells could not access EGFP+ podocytes. Conversely, when we induced nephrotoxic serum nephritis (NTSN) and injected Jedi T cells, EGFP+ podocyte transgenic mice showed enhanced proteinuria and higher blood urea levels. Morphometric analysis showed greater loss of EGFP+ podocytes, which was associated with severe crescentic and necrotizing glomerulonephritis. Notably, only glomeruli with disrupted Bowman’s capsule displayed massive CD8+ T cell infiltrates that were in direct contact with EGFP+ podocytes, causing their apoptosis. Thus, under control conditions with intact Bowman’s capsule, podocytes are not accessible to CD8+ T cells. However, breaches in Bowman’s capsule, as also noted in human crescentic glomerulonephritis, allow access of CD8+ T cells to the glomerular tuft and podocytes, resulting in their destruction. Through these mechanisms, a potentially reversible glomerulonephritis undergoes an augmentation process to a rapidly progressive glomerulonephritis, leading to end-stage kidney disease. Translating these mechanistic insights to human crescentic nephritis should direct future therapeutic interventions at blocking CD8+ T cells, especially in progressive stages of rapidly progressive glomerulonephritis.

Authors

Anqun Chen, Kyung Lee, Vivette D. D’Agati, Chengguo Wei, Jia Fu, Tian-Jun Guan, John Cijiang He, Detlef Schlondorff, Judith Agudo

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Figure 7

Immunohistologic analysis of CD8 in human biopsies with anti-GBM nephritis and ANCA-GN.

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Immunohistologic analysis of CD8 in human biopsies with anti-GBM nephrit...
(A–F) Representative images of CD8 immunohistochemistry. (A) CD8+ cells originating from the periglomerular interstitium infiltrate a cellular crescent through discrete ruptures of BC (arrow). PAS counterstain. Original magnification, ×600. (B) CD8+ cells (arrows) penetrate a cellular crescent through multiple small breaks in BC, which appears fragmented and discontinuous. PAS counterstain. Original magnification, ×600. (C) A CD8+ cell located deep within a crescent overlies a GBM, suggesting direct podocyte contact (arrow). PAS counterstain. Original magnification, ×600. (D) BC has a broad rupture involving more than half the glomerular circumference, associated with abundant CD8+ cells infiltrating the crescent from the adjacent interstitium. PAS counterstain. Original magnification, ×400. (E) A glomerulus with complete destruction of BC shows circumferential infiltration of its cellular crescent by numerous CD8+ cells and merging of the crescent with the adjacent interstitium. PAS counterstain. Original magnification, ×400. (F) A glomerulus with intact BC has no infiltrating CD8+ cells within its cellular crescent despite many CD8+ cells in the periglomerular interstitium. A single circulating CD8+ cell is present in a glomerular capillary. PAS counterstain. Original magnification, ×400. (G) Quantification of percentage of glomeruli with crescents, with ruptured BC with CD8 cells in the crescents, or with intact BC with CD8 cells in the crescents. APIGN, acute postinfectious glomerulonephritis; MGN, membranous glomerulonephritis. ****P < 0.0001.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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