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Preparation study of indocyanine green-rituximab: A new receptor-targeted tracer for sentinel lymph node in breast cancer

机译:吲哚菁绿-利妥昔单抗的制备研究:乳腺癌前哨淋巴结的新型受体靶向示踪剂

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摘要

An appropriate receptor-targeted tracer for sentinel lymph node biopsy (SLNB) was prepared. We combined the fluorescence tracer (Indocyanine green, ICG) with Rituximab (a chimeric human/murine monoclonal antibody targeting the CD20 antigen on the surface of lymphocyte) directly to produce a new tracer (ICG-Rituximab). When the new tracer drains to the lymph node, Rituximab will combine with CD20 receptor on the B-cell surface in the lymph node. If the statue of antibody-receptor connection does not reach saturation, the number of Rituximab is less than CD20. With this appropriate injection dose, the new tracer could only stay in sentinel lymph node (SLN) and make it imaging. Positive fluorescence SLN was detected 12 minutes after injection with no other organs imaging. The imaging of SLN was stable and clear for 20–24 hours. Due to SLN stained with more ICG than the lymphatic vessel, the fluorescence situation of SLN would be brighter than the vessel. The surgeon can detect the positive fluorescence SLN easily without following the fluorescence imaging lymphatic vessel. The results of our preliminary study showed that the new tracer might be useful for improving SLN imaging and worth further clinical study. SLNB with the new tracer could be a convenient method for detecting SLN and would become a standard performance in clinical practice.
机译:准备了合适的受体靶向示踪剂,用于前哨淋巴结活检(SLNB)。我们将荧光示踪剂(吲哚菁绿,ICG)与利妥昔单抗(靶向淋巴细胞表面CD20抗原的嵌合人/鼠单克隆抗体)直接结合,产生了新的示踪剂(ICG-利妥昔单抗)。当新的示踪剂排到淋巴结时,利妥昔单抗将与淋巴结B细胞表面的CD20受体结合。如果抗体-受体连接的状态未达到饱和,则利妥昔单抗的数量少于CD20。在适当的注射剂量下,新的示踪剂只能停留在前哨淋巴结(SLN)中并进行成像。注射后12分钟检测到阳性荧光SLN,没有其他器官成像。 SLN的成像在20-24小时内稳定且清晰。由于SLN染色的ICG比淋巴管的多,因此SLN的荧光情况会比血管亮。外科医生可以容易地检测出阳性荧光SLN,而无需跟踪荧光成像淋巴管。我们的初步研究结果表明,新的示踪剂可能对改善SLN成像有用,值得进一步的临床研究。带有新型示踪剂的SLNB可能是检测SLN的便捷方法,并将成为临床实践中的标准性能。

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