2002
Interleukin-2 Activation of Haematopoietic Stem Cells
HÁJEK, Roman; Zdeněk KOŘÍSTEK; Jana VINKLÁRKOVÁ; Eva JANOVSKÁ; Martin KLABUSAY et. al.Základní údaje
Originální název
Interleukin-2 Activation of Haematopoietic Stem Cells
Autoři
HÁJEK, Roman; Zdeněk KOŘÍSTEK; Jana VINKLÁRKOVÁ; Eva JANOVSKÁ; Martin KLABUSAY; Michael DOUBEK; D. DVOŘÁKOVÁ; Ludmila BOURKOVÁ; L. DUŠEK; Tomáš BÜCHLER; J. ADLER; Z. ADAM; Miroslav PENKA; Jiří MAYER a Jiří VORLÍČEK
Vydání
Acta Medica Austriaca, Berlin, BLACKWELL VERLAG GMBH, 2002, 0303-8173
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 0.293
Kód RIV
RIV/00216224:14110/02:00007781
Organizační jednotka
Lékařská fakulta
UT WoS
000175683600006
Klíčová slova anglicky
Immunotherapy; interleukin 2
Štítky
Změněno: 19. 5. 2003 15:49, Jana Mamulová
Anotace
V originále
BACKGROUND: Recent findings concerning the role of immunity in the eradication of residual malignant disease after autologous haematopoietic stem cell transplantation have led to extensive studies of T-cell and natural killer (NK) mediated anti-tumour effects. Interleukin 2 (IL-2) activation of autologous bone marrow (BM) or peripheral blood stem cells (PBSC) before transplantation is one of the methods of adoptive cell therapy. METHODS: Autologous BM of patients with chronic myelogenous leukaemia (n = 11) and PBSC of patients with multiple myeloma (n = 14) were activated by IL-2 in laboratory conditions with the aim of evaluating the feasibility of this method, the activation of T and NK cells, recovery of active progenitor cells, microbial contamination, and reduction of malignant cell content. RESULTS: Samples of BM (mean 2.6 x 10(6) cells) and PBSC (mean 10.3 x 10(6) cells) were cultured in complete culture medium with IL-2 (6000 Ul/ml) for 24 h. The recovery of CD34+ cells and CFU-GM was 82.5% and 51.5%, respectively, for BM, and 85% and 86%, respectively, for PBSC (mean values). No purging effect was detected by flow cytometry and a small decline in malignant cell contamination was observed by quantitative PCR in BM samples. No microbial contamination occurred during the sample processing. CONCLUSIONS: The described in vitro activation of BM and peripheral blood stem cells using IL-2 was evaluated as a safe and reliable method suitable for clinical application.
Návaznosti
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