Despite the progress made to improve therapeutic outcomes for acute myeloid leukemia(AML),many unmet clinical needs remain to be resolved.Unlike existing anti-AML strategies,here we developed a biomimetic nanocomposit...Despite the progress made to improve therapeutic outcomes for acute myeloid leukemia(AML),many unmet clinical needs remain to be resolved.Unlike existing anti-AML strategies,here we developed a biomimetic nanocomposite to efficiently eliminate the leukemia cells in the bone marrow and prevent the homing of AML.To fulfill our design,the ultra-small nanozyme was conjugated onto the surface of an oxygen-carrying nanoparticle,which was further coated with bone marrow stromal cell membrane.After entering the blood,this biomimetic nanocomposite got actively internalized by the leukemia cells in the blood and released the loaded chemotherapeutics and nanozyme inside the leukemia cells to achieve a synergistic antitumor efficacy.Meanwhile,the adhesive properties of the stromal cell membrane enabled the nanocomposite to home to the bone marrow,where the nanocomposite effectively killed the retained leukemia cells.More importantly,the biomimetic cell membrane also acted as a CXCR4 antagonism to block the CXCR4/CXCL12-mediated homing of leukemia cells to the bone marrow and infiltration to other organs like the liver and spleen.In conclusion,this proof-of-concept study demonstrated that our designed platform effectively kills leukemia cells while preventing their infiltration,thus providing a promising prospect for resolving the clinical challenges in current AML treatment.展开更多
基金the National Key Research and Development Program of China[No.2017YFA0205502]National Natural Science Foundation of China[No.82072067,61821002]the Fundamental Research Funds for the Central Universities.We acknowledge Prof.Haiyan Xu at the Institute of Basic Medical Sciences,Chinese Academy of Medical Sciences&Peking Union Medical College for assistance in the design of the animal study.
文摘Despite the progress made to improve therapeutic outcomes for acute myeloid leukemia(AML),many unmet clinical needs remain to be resolved.Unlike existing anti-AML strategies,here we developed a biomimetic nanocomposite to efficiently eliminate the leukemia cells in the bone marrow and prevent the homing of AML.To fulfill our design,the ultra-small nanozyme was conjugated onto the surface of an oxygen-carrying nanoparticle,which was further coated with bone marrow stromal cell membrane.After entering the blood,this biomimetic nanocomposite got actively internalized by the leukemia cells in the blood and released the loaded chemotherapeutics and nanozyme inside the leukemia cells to achieve a synergistic antitumor efficacy.Meanwhile,the adhesive properties of the stromal cell membrane enabled the nanocomposite to home to the bone marrow,where the nanocomposite effectively killed the retained leukemia cells.More importantly,the biomimetic cell membrane also acted as a CXCR4 antagonism to block the CXCR4/CXCL12-mediated homing of leukemia cells to the bone marrow and infiltration to other organs like the liver and spleen.In conclusion,this proof-of-concept study demonstrated that our designed platform effectively kills leukemia cells while preventing their infiltration,thus providing a promising prospect for resolving the clinical challenges in current AML treatment.
