Dendritic Cell-Triggered Immune Activation Goes along with Provision of (Leukemia-Specific) Integrin Beta 7-Expressing Immune Cells and Improved Antileukemic Processes

被引:6
作者
Rackl, Elias [1 ]
Li, Lin [1 ]
Klauer, Lara Kristina [1 ]
Ugur, Selda [1 ]
Pepeldjiyska, Elena [1 ]
Seidel, Corinna L. [2 ]
Gunsilius, Carina [1 ]
Weinmann, Melanie [1 ]
Doraneh-Gard, Fatemeh [1 ]
Reiter, Nina [1 ]
Plett, Caroline [1 ]
Amberger, Daniel Christoph [1 ]
Bojko, Peter [3 ]
Kraemer, Doris [4 ]
Schmohl, Joerg [5 ]
Rank, Andreas [6 ]
Schmid, Christoph [6 ]
Schmetzer, Helga Maria [1 ]
机构
[1] Univ Hosp Munich, Dept Med 3, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Orthodont & Dentofacial Orthoped, D-80336 Munich, Germany
[3] Rotkreuzklinikum Munich, Dept Hematol & Oncol, D-80634 Munich, Germany
[4] St Josefs Hosp, Dept Hematol & Oncol, D-58097 Hagen, Germany
[5] Diakonieklinikum Stuttgart, Dept Hematol & Oncol, D-70176 Stuttgart, Germany
[6] Univ Hosp Augsburg, Dept Hematol & Oncol, D-86156 Augsburg, Germany
关键词
integrin beta 7; leukemia-derived dendritic cells; immune therapy; AML; MDS; ACUTE MYELOID-LEUKEMIA; T-CELL; MYELODYSPLASTIC SYNDROME; CIK CELLS; AML; EXPRESSION; IDENTIFICATION; IMMUNOTHERAPY; VACCINATION; RESPONSES;
D O I
10.3390/ijms24010463
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Integrin beta 7 (beta 7), a subunit of the integrin receptor, is expressed on the surface of immune cells and mediates cell-cell adhesions and interactions, e.g., antitumor or autoimmune reactions. Here, we analyzed, whether the stimulation of immune cells by dendritic cells (of leukemic derivation in AML patients or of monocyte derivation in healthy donors) leads to increased/leukemia-specific beta 7 expression in immune cells after T-cell-enriched mixed lymphocyte culture-finally leading to improved antileukemic cytotoxicity. Healthy, as well as AML and MDS patients' whole blood (WB) was treated with Kit-M (granulocyte-macrophage colony-stimulating factor (GM-CSF) + prostaglandin E1 (PGE1)) or Kit-I (GM-CSF + Picibanil) in order to generate DCs (DCleu or monocyte-derived DC), which were then used as stimulator cells in MLC. To quantify antigen/leukemia-specific/antileukemic functionality, a degranulation assay (DEG), an intracellular cytokine assay (INTCYT) and a cytotoxicity fluorolysis assay (CTX) were used. (Leukemia-specific) cell subtypes were quantified via flow cytometry. The Kit treatment of WB (compared to the control) resulted in the generation of DC/DCleu, which induced increased activation of innate and adaptive cells after MLC. Kit-pretreated WB (vs. the control) led to significantly increased frequencies of beta 7-expressing T-cells, degranulating and intracellular cytokine-producing beta 7-expressing immune cells and, in patients' samples, increased blast lysis. Positive correlations were found between the Kit-M-mediated improvement of blast lysis (vs. the control) and frequencies of beta 7-expressing T-cells. Our findings indicate that DC-based immune therapies might be able to specifically activate the immune system against blasts going along with increased frequencies of (leukemia-specific) beta 7-expressing immune cells. Furthermore, beta 7 might qualify as a predictor for the efficiency and the success of AML and/or MDS therapies.
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页数:23
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