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
Categorie Soggetti
Pharmacology & Pharmacy","Medicine, Research & Experimental
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.