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排序方式: 共有2861条查询结果,搜索用时 15 毫秒
41.
Emmanuel de Billy Marsha Pellegrino Domenico Orlando Giulia Pericoli Roberta Ferretti Pietro Businaro Maria Antonietta Ajmone-Cat Sabrina Rossi Lucia Lisa Petrilli Nicola Maestro Francesca Diomedi-Camassei Marco Pezzullo Cristiano De Stefanis Paola Bencivenga Alessia Palma Rossella Rota Francesca Del Bufalo Luca Massimi Gerrit Weber Chris Jones Andrea Carai Simona Caruso Biagio De Angelis Ignazio Caruana Concetta Quintarelli Angela Mastronuzzi Franco Locatelli Maria Vinci 《Neuro-oncology》2022,24(7):1150
BackgroundDiffuse midline gliomas (DMG) H3K27M-mutant, including diffuse intrinsic pontine glioma (DIPG), are pediatric brain tumors associated with grim prognosis. Although GD2-CAR T-cells demonstrated significant anti-tumor activity against DMG H3K27M-mutant in vivo, a multimodal approach may be needed to more effectively treat patients. We investigated GD2 expression in DMG/DIPG and other pediatric high-grade gliomas (pHGG) and sought to identify chemical compounds that would enhance GD2-CAR T-cell anti-tumor efficacy.MethodsImmunohistochemistry in tumor tissue samples and immunofluorescence in primary patient-derived cell lines were performed to study GD2 expression. We developed a high-throughput cell-based assay to screen 42 kinase inhibitors in combination with GD2-CAR T-cells. Cell viability, western blots, flow-cytometry, real time PCR experiments, DIPG 3D culture models, and orthotopic xenograft model were applied to investigate the effect of selected compounds on DIPG cell death and CAR T-cell function.ResultsGD2 was heterogeneously, but widely, expressed in the tissue tested, while its expression was homogeneous and restricted to DMG/DIPG H3K27M-mutant cell lines. We identified dual IGF1R/IR antagonists, BMS-754807 and linsitinib, able to inhibit tumor cell viability at concentrations that do not affect CAR T-cells. Linsitinib, but not BMS-754807, decreases activation/exhaustion of GD2-CAR T-cells and increases their central memory profile. The enhanced anti-tumor activity of linsitinib/GD2-CAR T-cell combination was confirmed in DIPG models in vitro, ex vivo, and in vivo.ConclusionOur study supports the development of IGF1R/IR inhibitors to be used in combination with GD2-CAR T-cells for treating patients affected by DMG/DIPG and, potentially, by pHGG. 相似文献
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Gastric duplication cyst: CT and MRI findings in a case 总被引:1,自引:0,他引:1
44.
Filippo Monelli Francesco Venturelli Lisa Bonilauri Elisa Manicardi Valeria Manicardi Paolo Giorgi Rossi Marco Massari Guido Ligabue Nicoletta Riva Susanna Schianchi Efrem Bonelli Pierpaolo Pattacini Maria Chiara Bassi Giulia Besutti 《肝癌研究(英文版)》2021,7(4):13-24
Aim: In this systematic review, guidelines on non-alcoholic fatty liver disease (NAFLD) were evaluated, aiming at a guideline synthesis focusing on diagnosis an... 相似文献
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N. Bassi S. Zampieri A. Ghirardello M. Tonon M. Zen F. Cozzi A. Doria 《Clinical reviews in allergy & immunology》2009,37(1):36-43
Atherosclerosis is a disease of the vascular wall, which predominantly affects large and medium-sized arteries. It represents
a leading cause of morbidity and mortality in the Western world. In the last few decades, it has been clearly shown that immune
system plays a relevant role in atherogenesis. The effectors of both innate and adaptive immunity, including immune cells,
cell or soluble receptors, cytokines, chemokines, complement components or coagulation systems, and autoantibodies are able
to modulate atherosclerosis. Among proteins belonging to innate immunity, the highly conserved pentraxin family, which encompass
C-reactive protein (CRP), serum amyloid P (SAP), and the long pentraxin 3 (PTX3) seems to be directly involved in the induction
and progression of atherosclerosis. By immunohistochemical staining, pentraxins were found within the atherosclerotic plaques
where they could play a key role interacting with atherogenic-modified lipoproteins, favoring the formation of foam cells,
and exerting a proinflammatory action. Pentraxin serum levels have been shown to be associated with clinical and subclinical
atherosclerosis in general population. Antibodies against pentraxins have been demonstrated in patients with autoimmune diseases,
but their role in atherogenesis is still controversial. 相似文献
49.
Platelet reactivity in patients and recurrent events post-stenting: results of the PREPARE POST-STENTING Study. 总被引:7,自引:0,他引:7
Paul A Gurbel Kevin P Bliden Kirk Guyer Peter W Cho Kazi A Zaman Rolf P Kreutz Ashwani K Bassi Udaya S Tantry 《Journal of the American College of Cardiology》2005,46(10):1820-1826
OBJECTIVES: We investigated the relation of high ex vivo platelet reactivity, rapid fibrin generation, and high thrombin-induced clot strength to postdischarge ischemic events in patients undergoing percutaneous coronary intervention (PCI). BACKGROUND: High platelet reactivity and rapid fibrin generation may affect the incidence of ischemic events after PCI. However, limited data is available to link these ex vivo markers to the occurrence of events. METHODS: We measured platelet reactivity to adenosine diphosphate (ADP) by light transmittance aggregometry (LTA) in patients undergoing PCI (n = 192). Clot strength, a measure of thrombin-induced fibrin and platelet interactions, and the time to initial fibrin generation, a marker of thrombin activity, were measured by thrombelastography. The relation of these measurements to ischemic event occurrence was prospectively examined over six months. RESULTS: A total of 100% and 84% of patients were on aspirin and clopidogrel therapy, respectively, at the time of the initial event. Posttreatment ADP-induced aggregation by LTA (63 +/- 12% vs. 56 +/- 15%, p = 0.02) and clot strength (MA) were higher (74 +/- 5 mm vs. 65 +/- 4 mm, p < 0.001) and time to initial fibrin generation was shorter (4.3 +/- 1.3 min vs. 5.9 +/- 1.5 min, p < 0.001) in patients with events (n = 38). The event rates in the highest quartiles of LTA and MA were 32% and 58%, respectively. CONCLUSIONS: High platelet reactivity and clot strength, and rapid fibrin formation are novel risk factors for ischemic events after PCI. Clot strength is more predictive than ADP-induced platelet aggregation and may explain the occurrence of events despite treatment with cyclooxygenase-1 and P2Y12 inhibitors. 相似文献
50.
Elena Makovac Sarah N Garfinkel Andrea Bassi Barbara Basile Emiliano Macaluso Mara Cercignani Giovanni Calcagnini Eugenio Mattei Daniela Agalliu Pietro Cortelli Carlo Caltagirone Marco Bozzali Hugo Critchley 《Neuropsychopharmacology》2015,40(7):1649-1658
Autonomic nervous system activity is an important component of human emotion. Mental processes influence bodily physiology, which in turn feeds back to influence thoughts and feelings. Afferent cardiovascular signals from arterial baroreceptors in the carotid sinuses are processed within the brain and contribute to this two-way communication with the body. These carotid baroreceptors can be stimulated non-invasively by externally applying focal negative pressure bilaterally to the neck. In an experiment combining functional neuroimaging (fMRI) with carotid stimulation in healthy participants, we tested the hypothesis that manipulating afferent cardiovascular signals alters the central processing of emotional information (fearful and neutral facial expressions). Carotid stimulation, compared with sham stimulation, broadly attenuated activity across cortical and brainstem regions. Modulation of emotional processing was apparent as a significant expression-by-stimulation interaction within left amygdala, where responses during appraisal of fearful faces were selectively reduced by carotid stimulation. Moreover, activity reductions within insula, amygdala, and hippocampus correlated with the degree of stimulation-evoked change in the explicit emotional ratings of fearful faces. Across participants, individual differences in autonomic state (heart rate variability, a proxy measure of autonomic balance toward parasympathetic activity) predicted the extent to which carotid stimulation influenced neural (amygdala) responses during appraisal and subjective rating of fearful faces. Together our results provide mechanistic insight into the visceral component of emotion by identifying the neural substrates mediating cardiovascular influences on the processing of fear signals, potentially implicating central baroreflex mechanisms for anxiolytic treatment targets. 相似文献