FIELD: medicine.
SUBSTANCE: invention refers to biotechnology. The method includes the first phase of tumour-responsive CD4+ helpers and/or CD8+ T-lymphocytes stimulation by a tumour antigen together with at least one substance characterised as IL-2 receptor agonist, for increasing the viability of in viability tumour-responsive CD4+ helpers and/or CD8+ T-lymphocytes; and the second phase of tumour-responsive CD4+ helpers and/or CD8+ T-lymphocytes activation and growth intensification where the second phase is initiated by CD25 surface marker (or IL-2R marker) inhibition on CD4+ T-helpers and/or CD8+ T-lymphocytes. This method ensures a great quantity of tumour-responsive T-lymphocytes in a short span of time, and enables the directed evolution of tumour-responsive CD4+ helpers and/or CD8+ T-lymphocytes to specific subpopulations.
EFFECT: improved method for increasing tumour-responsive lymphocyte count and activating, particularly CD4+ helpers and/or CD8+ T-lymphocytes which can be applied in cancer treatment and/or prevention.
18 cl, 28 dwg, 1 tbl, 2 ex
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Authors
Dates
2010-09-20—Published
2006-12-20—Filed