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泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用

OBJECTIVE: To observe the cytotoxity of CD138-CAR-T cells on human multiple myeloma cell RPMI8226 and U266 cells and explore the impact of pomalidomide on the cytotoxity of CD138-CAR-T on RPMI8226 and U266 cells. METHODS: The cytotoxity of CD138-CAR-T and CD138-CAR-T combined pomalidomide on RPMI822...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343067/
https://www.ncbi.nlm.nih.gov/pubmed/26134016
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.06.011
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collection PubMed
description OBJECTIVE: To observe the cytotoxity of CD138-CAR-T cells on human multiple myeloma cell RPMI8226 and U266 cells and explore the impact of pomalidomide on the cytotoxity of CD138-CAR-T on RPMI8226 and U266 cells. METHODS: The cytotoxity of CD138-CAR-T and CD138-CAR-T combined pomalidomide on RPMI8226 and U266 was detected by CFSE/7AAD. The effctor cells were co-cultured with target cells at 5:1 for 18 h, and then the supernatant were collected and used for ELISA assays. RESULTS: After 18 h co-culture, the cytotoxity of CD138-CAR-T on RPMI8226 and U266 was significantiy higher than control (P<0.01). There was no significant change on the cytotoxity of pomalidoide combined with CD138-CAR-T on RPMI8226 and U266. The results showed that co-cultured system contribted to a markedly increased production of IFN-γ, after adding pomalidomide to the cocultured system. It can significantly enhance the production of IFN-γ, compared with CD138-CAR-T alone. CONCLUSION: CD138-CAR-T had significantly cytotoxity on U266 and RPMI8226. Pomalidomide could promote CD138-CAR-T cells IFN-γ production.
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spelling pubmed-73430672020-07-16 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To observe the cytotoxity of CD138-CAR-T cells on human multiple myeloma cell RPMI8226 and U266 cells and explore the impact of pomalidomide on the cytotoxity of CD138-CAR-T on RPMI8226 and U266 cells. METHODS: The cytotoxity of CD138-CAR-T and CD138-CAR-T combined pomalidomide on RPMI8226 and U266 was detected by CFSE/7AAD. The effctor cells were co-cultured with target cells at 5:1 for 18 h, and then the supernatant were collected and used for ELISA assays. RESULTS: After 18 h co-culture, the cytotoxity of CD138-CAR-T on RPMI8226 and U266 was significantiy higher than control (P<0.01). There was no significant change on the cytotoxity of pomalidoide combined with CD138-CAR-T on RPMI8226 and U266. The results showed that co-cultured system contribted to a markedly increased production of IFN-γ, after adding pomalidomide to the cocultured system. It can significantly enhance the production of IFN-γ, compared with CD138-CAR-T alone. CONCLUSION: CD138-CAR-T had significantly cytotoxity on U266 and RPMI8226. Pomalidomide could promote CD138-CAR-T cells IFN-γ production. Editorial office of Chinese Journal of Hematology 2015-06 /pmc/articles/PMC7343067/ /pubmed/26134016 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.06.011 Text en 2015年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title_full 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title_fullStr 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title_full_unstemmed 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title_short 泊马度胺联合CAR-T细胞对多发性骨髓瘤细胞株RPMI8226、U266细胞的体外杀伤作用
title_sort 泊马度胺联合car-t细胞对多发性骨髓瘤细胞株rpmi8226、u266细胞的体外杀伤作用
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343067/
https://www.ncbi.nlm.nih.gov/pubmed/26134016
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.06.011
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