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免疫循环与介入治疗:T淋巴细胞向肿瘤浸润

时间:2021-01-30 15:57来源:未知 作者:admin
RFA (or TACE) + Anti-CTLA4 Checkpoint Inhibitor for HCC 12/14 HCV Reduced viral load Reduced AFP,6 week biopsy: CD8 up only if response 57% PFS @ 6 mo heavily pre-treated pts 消融和Anti-CTLA4后远处肿瘤的镜下表现 Baseline Immune infiltrate


RFA (or TACE) + Anti-CTLA4 Checkpoint Inhibitor for HCC


基线 9个月后


   
12/14 HCV Reduced viral load  Reduced AFP,6 week biopsy: CD8 up only if response 57% PFS @ 6 mo – heavily pre-treated pts
 

消融和Anti-CTLA4后远处肿瘤的镜下表现
Baseline
Immune infiltrate
Remote tumor Post Anti-CTLA4 & Ablation


Can see pseudoprogression on  CT / MRI as a result of an  immunologic infiltrate,More robust T cell infiltration in  responders
 


Greten & Duffy  ASCO 2015, ASCO GI 2016, J Heptology 2016


Antigen Presentation at Margin of RFA
 
CD11C→ APC (green)
DAPI→nuclei (blue)

RFA plus DC CD11C IF staining
 
Fusion image
APC’s = Green



对照 射频消融 树突细胞 射频+树突细胞

荧光显微镜下可见CD11c抗原提呈细胞(DC)在射频消融、ITDC和联合治疗后用FITC标记的CD11c抗体进行免疫组化检测。治疗后11天,取肿瘤,纵向分离,进行免疫组织化学分析。抗原提呈细胞(绿色),用4‘,6-二胺-2-苯基吲哚(蓝色)染色.对照组肿瘤中抗原提呈细胞较少。相反,射频消融、ITDC和联合治疗的肿瘤CD11c染色水平均较高,提示治疗可增强肿瘤的DC浸润。
 

Dromi et al. Radiology 2009; 251: 58-66
 
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