1.Target Selection of CAR-T Therapy in Acute Myeloid Leukemia——Review
Ruo-Nan SHAO ; Hong-Lei XIN ; Xiao-Feng SHI
Journal of Experimental Hematology 2024;32(3):965-969
Chimeric antigen receptor(CAR)T cell therapy,one of the most promising tumor treatments,combines the targeted recognition of antigen and antibody with the killing effect of T cells.CAR-T has shown a strong therapeutic effect in lymphoid tumors and been applied in clinical practice.However,in the treatment of acute myeloid leukemia(AML),no effective and specific target like CD 19 in lymphoid tumors has been found.Therefore,the key research direction is to try multiple probabilities and use optimization strategies to enhance efficacy and reduce toxicity.This review introduces the latest research progress of AML targets in CAR-T therapy in recent years,analyzes the related problems that need to be solved at present,and summarizes the optimization construction strategies mentioned in the research.Hope it can provide reference for related research and clinical application of related product.
2.A clarifying method that improves imaging of Aplysia ganglia.
Ting-Ting CHEN ; Wei YU ; Dan-Dan LIU ; Ke YU ; Song-An CHEN ; Ye WANG ; Shao-Zhong YANG ; Ruo-Nan JIA ; Yu-Tong ZHENG ; Zhen HUANG ; Ferdinand S VILIM ; Lei DONG ; Elizabeth C CROPPER ; Klaudiusz R WEISS ; Jian JING
Acta Physiologica Sinica 2017;69(4):461-466
Improvements in the imaging of neural circuits are essential for studies of network function in both invertebrates and vertebrates. Therefore, CLARITY, a new imaging enhancement technique developed for mouse brains has attracted broad interest from researchers working on other species. We studied the potential of a modified version of CLARITY to enhance the imaging of ganglia in an invertebrate Aplysia. For example, we have modified the hydrogel solution and designed a small container for the Aplysia ganglia. The ganglia were first processed for immunohistochemistry, and then for CLARITY. We examined the compatibility of these techniques and the extent to which the imaging of fluorescence improved using confocal microscopy. We found that CLARITY did indeed enhance the imaging of CP2 immunopositive neurons in Aplysia ganglia. For example, it improved visualization of small, weak immunoreactive neurons deep in the ganglia. Our modifications of CLARITY make this new method suitable for future use in Aplysia experiments. Furthermore, our techniques are likely to facilitate imaging in other invertebrate ganglia.

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