Histone deacetylase inhibitors prevent activation of tumour-reactive NK cells and T cells but do not interfere with their cytolytic effector functions.

Abstract:

:Histone deacetylase inhibitors (HDIs) exert direct tumour-toxic activity and sensitise tumour cells for other therapeutic regimens as well as the cytotoxic effects of activated immune cells. However, the HDI suberoylanilide hydroxamic acid (SAHA; vorinostat) interfered with the IL-2 activation of human NK cells and the priming of human tumour-specific T cells. In contrast, NK or T cells which were activated in the absence of HDIs became resistant to their immunosuppressive action. Therefore, as a therapeutic strategy, first the patient's immune system might be stimulated and then HDIs could sensitise the tumours for the attack of the pre-activated immune effector cells.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Schmudde M,Friebe E,Sonnemann J,Beck JF,Bröker BM

doi

10.1016/j.canlet.2010.02.024

subject

Has Abstract

pub_date

2010-09-28 00:00:00

pages

173-81

issue

2

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(10)00134-5

journal_volume

295

pub_type

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