Generation of Functional CLL-Specific Cord Blood CTL Using CD40-Ligated CLL APC

被引:6
作者
Decker, William K. [1 ]
Shah, Nina [2 ]
Xing, Dongxia [2 ]
Lapushin, Ruth [3 ]
Li, Sufang [2 ]
Robinson, Simon N. [2 ]
Yang, Hong [2 ]
Parmar, Simrit [2 ]
Halpert, Matthew M. [1 ]
Keating, Michael J. [3 ]
Gribben, John G. [4 ]
Molldrem, Jeffrey J. [2 ]
Shpall, Elizabeth J. [2 ]
Wierda, William G. [3 ]
机构
[1] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[4] Barts & London Queen Marys Sch Med & Dent, Inst Canc, London, England
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; STEM-CELL TRANSPLANTATION; IMMUNOLOGICAL SYNAPSE FORMATION; GRAFT-VERSUS-LEUKEMIA; ALLOREACTIVE T-CELLS; CLASS-I; B-CLL; THERAPY; IMMUNODEFICIENCY; IMMUNOTHERAPY;
D O I
10.1371/journal.pone.0051390
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced requirements for stringent HLA matching between graft and recipient; however, disease relapse remains a concern with this modality. The generation of CLL-specific CTL from UCB T-cells, primed and expanded against the leukemic clone, might enhance the GVL effect and improve outcomes with UCB transplantation. Here we report the generation of functional, CLL-specific CTL using CD40-ligated CLL cells to prime partially-HLA matched UCB T-cells. Functionality and specificity were demonstrated by immune synapse assay, IFN-gamma ELISpot, multi-parametric intracellular cytokine flow cytometry, and Cr-51 release assay. The use of patient-specific, non-CLL controls demonstrated the generation of both alloantigen and CLL-specific responses. Subsequently, we developed a clinically-applicable procedure permitting separation of alloreactive CTL from leukemia-specific CTL. Leukemia-specific CTL were able to mediate in vivo killing of CLL in humanized mice without concurrent or subsequent development of xenoGVHD. Our results demonstrate that generation of CLL-specific effectors from UCB is feasible and practical, and the results support further exploration of this strategy as a treatment modality for CLL.
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页数:14
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