Clinical-grade functional dendritic cells from patients with multiple myeloma are not infected with Kaposi's sarcoma-associated herpesvirus

被引:58
作者
Tarte, K
Olsen, SJ
Lu, ZY
Legouffe, E
Rossi, JF
Chang, Y
Klein, B
机构
[1] CNRS, Inst Mol Genet, F-34033 Montpellier, France
[2] Columbia Univ, Sch Publ Hlth, Div Epidemiol, New York, NY USA
[3] CHU Montpellier, Hop St Eloi, Unit Cellular Therapy, Montpellier, France
[4] CHU Montpellier, Hop Lapeyronie, Serv Malad Sang B, Montpellier, France
[5] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY USA
关键词
D O I
10.1182/blood.V91.6.1852.1852_1852_1857
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone marrow dendritic cells (DC) from patients with multiple myeloma (MM) were recently reported to be infected with Kaposi's sarcoma-associated herpesvirus (KSHV). Because immunotherapy strategies using DC are very promising in this disease, we looked for KSHV DNA in clinical-grade DC generated in vitro from MM patients. Adherent apheresis cells from MM patients were maintained for 7 days in clinical-grade X-VIVO 15 culture medium supplemented with granulocyte-macrophage colony-stimulating factor, interleukin-4, or interleukin-13. Tumor necrosis factor alpha was added for the last 2 days. We obtained a cell population with a DC phenotype able to endocytose fluorescein isothiocyanate (FITC)-dextran and efficiently activate resting allogenic T lymphocytes. To detect KSHV DNA, we used polymerase chain reaction (PCR) followed by Southern blotting of PCR product with a sensitivity detecting a few copies of viral DNA, All the PCR were repeated in a blinded fashion three times, on 1 mu g and 0.2 mu g of genomic DNA, in two different laboratories. Clinical-grade DC from 10 (91%) of 11 patients were not infected with KSHV. The apheresis cells and the purified CD34(+) cells from the same patients were also negative, A very weak PCR hand was detected with DC from one patient, but the initial apheresis cells were negative. The detection of KSHV infection in 1 (9%) of 11 MM patients probably represents background seroprevalence. It seems likely that functional and clinical-grade DC from MM patients can safely be used in clinical trials. (C) 1998 by The American Society of Hematology.
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页码:1852 / 1857
页数:6
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