€
ss*
ffiffi*xftg.zE,
-#F,1
nfrffift,trtatrS*
-
gtJ.lHH#t+E
BJFR+t€€F=fEf4f+eDt
ffi
EEf
ffi
*H
ftifrW^
r
oz
€f
ffi
ff
llEt(
#plt*fftr+,u'€H^
'
HEre*
.
Ezffiffin*ry€a
"
+4?G=FE
ffinEryffi*,
a.ffifrEnF
-
ffiffi
wnffifrH.BBoffim
"
ft&fr'€^w
ffi.*?Nn;F...4
Sto..y
Brook
HfEEf
ffi
ErE
F,rl.
.
W+EiXJbte#4
ff
*ffi
re+ffi
Rffi
fr,
t:+F'
fr+*re#ffiffi
nE4*6tr
F0tr
X
"
E.ffiffifr-EffrffiffJffif-+
'
$fiilfmfiFl
"#e'ffffi"
ffi
"
MffilbtF"
o
E$Ct#fFfiff#€,*fi1'
E#"
+ffi&.U
4,Wfflffifu+F0ffi4*4ffifr*"
;
&+#*.&lmtH'
I&8
"
U
nErfr#Hffi
n0ffi
elF
ffiE
*,
ffi#fr.8*e#8,6ffi
Fi
"E
#"
"
EiltgE*ff ffifr.fgffi"B€-HilIn"
FoFHU'
P]&."8
T
ffiN*#ftEfr
ffi
ffif|]${
NffifrHB
NOffi
M'
+#
EI
##
j*#HruJYB
ffiWq.3o7
€f
ffi
ffi
ffi
tuEWXffi
,
F'sj#.#M.
+Bb
'ff*HAffi##tt
"
ffi
Ffi
gI
+T
fg,fEl
H
tr F *, F,i6F.
Z
ffi@ft,E)AH
' E+HiE,E6+E€-i{f!trt
'
ffiB
d,#*ltH,\
We
HtuEAffi
, l*FtJilr#ild#)HtrtgffiBAH!
-E)6ffit
i*
"
rF,.ft
Ht
wg
ft,E
ElH
f.,t
f! tr
tg
tuE
.
rH.ft
fr,
E
e
ffi
+_wJ
'afrf,ht={n
-WilrEWJ
'
EEien,\EgEE-}I '
4*EHt*lnf
{EtuEeE
h
"
tft1
e
I
3
+44*)
|E+E
H
4
Wr
F.re{6EAt
(biologic response modifiers)
tr-{ffe
,
rH,ftHtEtgftF-)e
HE,ffi
trtr
7
g+
++^tr#tr*
Hlf
E,
6,ffii9t$Eitf-nlf,
.
ffi
flEtr
+'
+n)Ei{G*HflE'
i-n,E}iF€'
tgHE
Etr)hFS6
'fEtm
H!fiff
4AF€-R
H
Ht
Etrr,
lEEffi
fl
ffi
ft
6ff
f;
ffi''fEttri
fi]ry€
7
EJE
FIFIR'
HE-i{
H!
Fffi
ft DE'9fr,tr'6HFE
7
IE
ffifflH,EEffi
"
)EEF.
r+ml
Fung Kwong Chuen
A
RISING STAR
FOR
CANCER THERAPY:
INTERVIEW
WITH
PROF LIU
GUANGXIAN,
CANCER
IMMUNOTHERAPY
SPECIALIST
Cancer immunotherapy,
a
fast
developing modality,
involves cell
factors
controlling
cell
growth and
development, e.9.,
growth
factors
and interferons. Tumor-associated
antigens
(TAAs) are
cell surface pro-
teins of
immature host tissues, e.9.,
alpha
fetal
protein
(AFP)
and
carcinoembryonic antigen (CEA); tu-
mor specific antigens (TSAs)
are
novel and specific
antigens
of the
tumor itself and "foreign"
to
the
host.
Antigen-presenting cells
(APC), no-
tably
dendritic
cells
(DC)
are
promising. Development
of cancer-
specific cytotoxic
T
lymphocyte
(CTL) clones are also feasible
and
are exploited in
the
process of
ac-
quiring specific antigens. CTL
and
tumor infiltrating lymphocytes
(TlL)
work on specific mechanisms whilst
cytokine-induced killer (ClK)
cells
work in a non-specific yet effective
manner. Lymphokine-activated killer
(LAK) cells of
the
Natural killer (NK)
category
have
a broad spectrum
of
cell
kill. As
a
promising
modality,
methods of tumor vaccines
vary.
Vaccines derived from tumors are
often
modified
genetically.
Short
pep-
tides fitting
into a
groove
in
the
ma-
jor histocompatibility complex (MHC)
molecule
are also
exploited
as
vaccines. Nucleic acid (DNA & RNA)
vaccines also hold promise.
--Ph
gil
-il|
glj