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◆ JACC. Advances2026-09-24

Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Pathway in High-Risk Lymphocytic Acute Myocarditis.

Enrico Ammirati, Guglielmo Gallone, Giacomo Veronese, Eric D Adler, Mikko I Mäyränpää, Emanuela Bonoldi, Duccio Petrella, Paul J Kim, Michela Brambatti, Matteo Pio Vaira, Meike Rybczynski, Hendrik Milting, Ina Michel-Behnke, Fernando Gatto, Florian Schlotter, Holger Thiele, Jose Benjamin Cruz Rodriguez, Andreas Luchner, Ulrich Grabmaier, Steffen Massberg, Herwig Schuchlenz, Christian Ebner, Tienush Rassaf, Axel Linke, Bettina Heidecker, Tatiana Manuylova, Andrea Garascia, Javid J Moslehi, Jukka Y Lehtonen, Karin Klingel

一句话结论 · In one sentence

PD-L1 is overexpressed in cardiomyocytes of patients with LAM compared with non-Infl-CMP or focal non-lymphocytic myocarditis, such as CS, suggesting that cardiac PD-L1 expression is likely a response to T-cell-mediated injury. PD-1 expression is blunted in infiltrating inflammatory cells in LAM compared with ACR, suggesting a disruption of the PD-L1/PD-1 axis in LAM.

原始摘要(英文原文)· Original abstract
BACKGROUND: The programmed cell death-1 (PD-1)/programmed cell death-ligand-1 (PD-L1) pathway is affected in immune checkpoint inhibitor (ICI)-associated acute myocarditis (AM), while this pathway in non-ICI-associated lymphocytic AM (LAM) is unexplored. OBJECTIVES: This study aimed to assess cardiac levels of PD-L1/PD-1 in patients with high-risk LAM, compared with cardiac sarcoidosis (CS), non-inflammatory cardiomyopathy (non-Infl CMP), ICI-AM, and acute cellular rejection (ACR). METHODS: PD-L1 expression was measured with a visual semiquantitative scale from 0 (0%) to 5 (≥75% of cardiomyocytes), and PD-1 from 0 (0%) to 5 (≥75% of inflammatory cells) in 142 patients with cardiac histology. We compared patients with LAM (n = 39), CS (n = 26), non-InflCMP (n = 11). As an additional group, we included 8 patients with ICI-AM. Finally, the expression of PD-L1/PD-1 was also evaluated in heart transplant recipients with ACR of grade ≥2R (n = 28) or no ACR (n = 30). RESULTS: Patients with LAM had increased median levels of PD-L1 compared with CS or non-Infl-CMP: 2 (first to third quartile: 2-3) vs 1 (1-2) vs 0 (0-0), respectively; P < 0.0001. Likewise, PD-L1 expression was higher in those with ACR ≥2R vs no ACR. Conversely, PD-1 was blunted in LAM compared to ACR ≥2R. Patients with LAM had similar cardiac PD-L1 expression but reduced cardiac PD-1 expression compared with ICI-AM. CONCLUSIONS: PD-L1 is overexpressed in cardiomyocytes of patients with LAM compared with non-Infl-CMP or focal non-lymphocytic myocarditis, such as CS, suggesting that cardiac PD-L1 expression is likely a response to T-cell-mediated injury. PD-1 expression is blunted in infiltrating inflammatory cells in LAM compared with ACR, suggesting a disruption of the PD-L1/PD-1 axis in LAM.
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Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Pathway in High-Risk Lymphocytic Acute Myocarditis. — 科研速览 Science Skim