Inhibition of acute myeloid leukemia cell growth by mono-specific and bi-specific anti-CD33 x anti-CD64 antibodies.

Abstract:

:Bi-specific anti-CD33 x anti-CD64 antibodies (BsAb) mediated more potent and longer-lasting inhibition of proliferation of human leukemia cell lines and primary acute myeloid leukemia (AML) samples compared to mono-specific anti-CD33 mAb. There were no differences between these two antibodies in cellular internalization over time. The inhibitory effect of BsAb was mimicked by a mouse IgG2a subclass mono-specific anti-CD33 mAb. These findings indicate that enhanced inhibition of proliferation was caused by simultaneous ligation of both CD33 and CD64 molecules. We conclude that inhibition of leukemia cell growth initiated by BsAb during prolonged exposure may have therapeutic value for the treatment of AML.

journal_name

Leuk Res

journal_title

Leukemia research

authors

Balaian L,Ball ED

doi

10.1016/j.leukres.2003.12.001

keywords:

subject

Has Abstract

pub_date

2004-08-01 00:00:00

pages

821-9

issue

8

eissn

0145-2126

issn

1873-5835

pii

S0145212603004120

journal_volume

28

pub_type

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