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Immunogenic cell death effects induced by doxorubicin improved chemo-immunotherapy via restoration of granzyme B activity
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作者 Tao Huang Xiaofan Sun +9 位作者 Yingqiu Qi Xi Yang Linyao Fan Mengdie Chen Yale Yue Hong Ge Yiye Li Guangjun Nie Huan Min Xianfu Sun 《Nano Research》 SCIE EI CSCD 2023年第12期13250-13258,共9页
Chemotherapy remains one of the irreplaceable treatments for cancer therapy.The use of immunogenic cell death(ICD)-inducing chemotherapeutic drugs offers a practical strategy for killing cancer cells,simultaneously el... Chemotherapy remains one of the irreplaceable treatments for cancer therapy.The use of immunogenic cell death(ICD)-inducing chemotherapeutic drugs offers a practical strategy for killing cancer cells,simultaneously eliciting an antitumor immune response by promoting the recruitment of cytotoxic immune cells and production of granzyme B(GrB).However,numerous malignant cancers adaptively acquired the capacity of secreting serpinb9(Sb9),a physiological inhibitor of GrB,which can reversibly inhibit the biological activity of GrB.To circumvent this dilemma,in this study,an integrated tailor-made nanomedicine composed of tumor-targeting peptide(Arg-Gly-Asp,RGD)decorated liposome,doxorubicin(DOX,an effective ICD inducer),and the compound 3034(an inhibitor of Sb9),is developed(termed as D3RL)for breast cancer chemo-immunotherapy.In vitro and in vivo studies show that D3RL can directly kill tumor cells and trigger the host immune response by inducing ICD.Meanwhile,D3RL can competitively relieve the inhibition of Sb9 to GrB.The restored GrB can not only effectively induce tumor immunotherapy,but also degrade matrix components in the tumor microenvironment,consequently improving the infiltration of immune cells and the penetration of nanomedicines,which in return enhance the combined antitumor effect.Taken together,this work develops an integrated therapeutic solution for targeted production and restoration of GrB to achieve a combined chemo-immunotherapy for breast cancer. 展开更多
关键词 immunogenic cell death granzyme b serpinb9 CHEMO-IMMUNOTHERAPY NANOMEDICINE
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活动性结核病患者自然杀伤(NK)细胞CD160的表达及其与细胞功能的关系
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作者 杨秉芬 翟斐 +4 位作者 安红娟 曹志红 刘艳华 王若 程小星 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2022年第10期918-924,共7页
目的分析外周血单个核细胞(PBMC)中CD160 mRNA和蛋白的表达与结核病免疫的关系。方法使用荧光定量PCR检测PBMC中CD160 mRNA的表达,流式细胞术分析PBMC中主要细胞群(T细胞、B细胞、自然杀伤(NK)细胞和单核细胞)表面CD160蛋白表达情况,使... 目的分析外周血单个核细胞(PBMC)中CD160 mRNA和蛋白的表达与结核病免疫的关系。方法使用荧光定量PCR检测PBMC中CD160 mRNA的表达,流式细胞术分析PBMC中主要细胞群(T细胞、B细胞、自然杀伤(NK)细胞和单核细胞)表面CD160蛋白表达情况,使用流式细胞术分析NK细胞中CD160与穿孔素(perforin)、颗粒酶B(granzyme B)、颗粒溶素(granulysin)、CD69、CD107和γ干扰素(IFN-γ)的关系。结果活动性肺结核患者PBMC中CD160 mRNA表达显著性下调,且结核分枝杆菌(MTB)阳性患者显著低于MTB阴性患者;B细胞和单核细胞表面CD160表达比例低;CD3^(+)T细胞表面CD160表达在活动性肺结核患者和正常对照者之间差异不明显;活动性肺结核患者NK细胞表面CD160表达显著低于正常对照者;NK细胞与MTB抗原体外培养可下调NK细胞表面CD160的表达;活动性肺结核患者NK细胞表面活化标志CD69表达显著低于正常对照者;CD160^(+)NK细胞的perforin、granzyme B、granulysin、CD69和CD107表达都显著高于CD160^(-)NK细胞;但是CD160^(+)NK细胞的IFN-γ表达显著低于CD160^(-)NK细胞。结论活动性肺结核患者CD160 mRNA和蛋白表达显著下调,CD160促进NK细胞与结核抗原相关的活化和脱颗粒,抑制NK细胞的IFN-γ的表达,CD160可能成为结核病诊治的新靶标。 展开更多
关键词 肺结核 NK细胞 CD160 γ干扰素(IFN-γ) 穿孔素(perforin) 颗粒酶b(granzyme b) 颗粒溶素(granulysin) CD69 CD107
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