A FEASIBLE METHOD FOR EXPANSION OF PERIPHERAL-BLOOD LYMPHOCYTES BY CULTURE WITH IMMOBILIZED ANTI-CD3 MONOCLONAL-ANTIBODY AND INTERLEUKIN-2 FOR USE IN ADOPTIVE IMMUNOTHERAPY OF CANCER-PATIENTS

Citation
T. Sekine et al., A FEASIBLE METHOD FOR EXPANSION OF PERIPHERAL-BLOOD LYMPHOCYTES BY CULTURE WITH IMMOBILIZED ANTI-CD3 MONOCLONAL-ANTIBODY AND INTERLEUKIN-2 FOR USE IN ADOPTIVE IMMUNOTHERAPY OF CANCER-PATIENTS, Biomedicine & pharmacotherapy, 47(2-3), 1993, pp. 73-78
Citations number
12
Categorie Soggetti
Pharmacology & Pharmacy","Medicine, Research & Experimental
ISSN journal
07533322
Volume
47
Issue
2-3
Year of publication
1993
Pages
73 - 78
Database
ISI
SICI code
0753-3322(1993)47:2-3<73:AFMFEO>2.0.ZU;2-1
Abstract
Cultivation of T lymphocytes with immobilized anti-CD3 monoclonal anti body and human recombinant interleukin-2 induced a rapid proliferative response. This procedure was applied to expansion culture of peripher al blood lymphocytes obtained from cancer patients for use in adoptive immunotherapy. Peripheral blood mononuclear cells were separated from 20 ml of blood and cultured in anti-CD3 coated flasks with rIL-2 for 6 days, then transferred to a gas-permeable culture bag and culture co ntinued for an additional 8 days with an increasing volume of medium. Cell numbers increased about 2000-fold during this 2-week culture. The final population contained about 30% CD4+ and 60% CD8+ cells. and all were CD3+ & HLA-DR+. NK cells comprised less than 5%. In clinical tri als involving 12 cases receiving 35 infusions, the mean number of harv ested T cells after 14 days culture was 3.5 x 10(10) (R = 1.6-6.8 x 10 (10)), and the mean expansion index was 1560-fold (R = 409-4091). This method could be of benefit not only in immunotherapy but also for obt aining somatic cells from a small volume of blood for use in molecular or genetic analysis instead of having to perform EB virus transformat ion of B cells.