Usefulness of IL-21, IL-7, and IL-15 conditioned media for expansion of antigen-specific CD8+T cells from healthy donor-PBMCs suitable for immunotherapy

被引:8
|
作者
Chamucero-Millares, Julian A. [1 ,2 ]
Bernal-Estevez, David A. [2 ]
Parra-Lopez, Carlos A. [1 ]
机构
[1] Univ Nacl Colombia, Sch Med, Dept Microbiol, Immunol & Translat Med Res Grp, Carrera 30 45-03, Bogota, South America, Colombia
[2] Fdn Salud Los Andes, Immunol & Clin Oncol Res Grp, Carrera 44 58-05, Bogota, South America, Colombia
关键词
Antigen-specific T cells; Monocyte-derived dendritic cells; Dendritic cell-based immunotherapy; Adoptive cell transfer; Cancer immunotherapy; Viral immunity; CD8 T cell; Immunological memory;
D O I
10.1016/j.cellimm.2020.104257
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clonal anergy and depletion of antigen-specific CD8+ T cells are characteristics of immunosuppressed patients such as cancer and post-transplant patients. This has promoted translational research on the adoptive transfer of T cells to restore the antigen-specific cellular immunity in these patients. In the present work, we compared the capability of PBMCs and two types of mature monocyte-derived DCs (moDCs) to prime and to expand ex-vivo antigen-specific CD8+ T cells using culture conditioned media supplemented with IL-7, IL-15, and IL-21. The data obtained suggest that protocols involving moDCs are as efficient as PBMCs-based cultures in expanding antigen-specific CD8+ T cell to ELA and CMV model epitopes. These three gamma common chain cytokines promote the expansion of naive-like and central memory CD8+ T cells in PBMCs-based cultures and the expansion of effector memory T cells when moDCs were used. Our results provide new insights into the use of media supplemented with IL-7, IL-15, and IL-21 for the in-vitro expansion of early-differentiated antigen-specific CD8+ T cells for immunotherapy purposes.y
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页数:11
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