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Upregulation of NKG2D ligands in acute lymphoblastic leukemia and non-Hodgkin lymphoma cells by romidepsin and enhanced in vitro and in vivo natural killer cell cytotoxicity.
[severe combined immunodeficiency]
There
is
a
critical
need
to
prevent
and
/
or
treat
hematological
relapse
after
allogeneic
hematopoietic
stem
cell
transplantation
.
The
activating
NKG
2
D
receptor
expressed
on
natural
killer
(
NK
)
cells
,
when
engaged
by
its
corresponding
ligands
(
MIC
A
/
B
)
,
activates
NK
cells
to
become
cytotoxic
against
malignant
cells
.
We
incubated
acute
lymphoblastic
leukemia
and
non-
Hodgkin
lymphoma
cells
for
24
h
with
10
ng
/
mL
of
romidepsin
.
Flow
cytometry
was
performed
to
demonstrate
changes
in
surface
expression
of
NKG
2
D
ligands
MIC
A
/
B
.
In
vitro
and
in
vivo
cytotoxicity
was
measured
by
means
of
modified
Europium
assay
,
and
non-obese
diabetic
/
severe
combined
immunodeficiency
mice
were
xenografted
with
RS
4
:
11
cells
.
We
demonstrated
an
approximately
50
,
200
,
1300
and
180
-
fold
increase
in
the
number
of
cells
positive
for
the
surface
expression
of
MIC
A
/
B
in
RS
4
:
11
(
P
Â
<
0
.
001
)
,
REH
(
P
Â
<
0
.
001
)
,
Ramos
(
P
Â
<
Â
0
.
001
)
and
Jurkat
cells
(
P
Â
<
0
.
001
)
,
respectively
.
We
further
demonstrated
a
significant
increase
in
NK
cell-mediated
in
vitro
cytotoxicity
against
RS
4
:
11
(
P
Â
<
0
.
004
)
,
Ramos
(
P
Â
<
0
.
05
)
,
Jurkat
(
P
Â
<
0
.
001
)
and
REH
cells
(
P
Â
<
0
.
01
)
,
respectively
.
Romidepsin-mediated
NK
cytotoxicity
was
blocked
by
pre-incubating
NK
cells
with
anti-
NKG
2
D
-Fc
in
RS
4
:
11
(
P
Â
<
0
.
03
)
and
Ramos
cells
(
P
Â
<
0
.
01
)
,
respectively
.
Finally
,
non-obese
diabetic
/
severe
combined
immunodeficiency
mice
xenografted
with
RS
4
:
11
cells
had
a
significant
increase
in
survival
(
P
Â
<
0
.
02
)
in
mice
treated
with
romidepsin
and
interleukin-
2
-
activated
NK
cells
compared
with
each
of
these
other
treatment
groups
.
Romidepsin
significantly
enhanced
in
vitro
and
in
vivo
NK
cell
cytotoxicity
mediated
in
part
by
increased
MIC
A
/
B
expression
on
malignant
cells
.
This
translational
approach
of
the
use
of
romidepsin
and
interleukin-
2
-
activated
NK
cells
should
be
considered
in
patients
with
relapsed
/
refractory
leukemia
or
lymphoma
.
Diseases
Validation
Diseases presenting
"malignant cells"
symptom
focal myositis
hodgkin lymphoma, classical
oral submucous fibrosis
pleomorphic liposarcoma
severe combined immunodeficiency
systemic capillary leak syndrome
waldenström macroglobulinemia
werner syndrome
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