COVER STORY
32 THE WEEK · JULY 29, 2018
HEALTH
C
ancer vaccines are
back in the headlines
with research teams
from Stanford Uni-
versity School of Medicine pub-
lishing breakthrough results of
immunotherapy studies. Cancer
research seems to be experienc-
ing a tidal wave of immuno-
therapy treatment options; the
excitement around the US Food
and Drug Administration ap-
proval of the fi rst CAR T-cell
therapy and then a second one
within months, is still afresh.
The Stanford teams are taking
this to a new level by pressing
all the right buttons for a cancer
vaccine.
This February, an interest-
ing study led by researchers
at the university has shown
experimental vaccines as pos-
sible treatments for cancers in
mice, and the university is start-
ing human trials soon.
Stimulating immune system
against solid tumours
The study injected minute
amounts of two immune-stim-
ulating agents directly into solid
Taking it to
the next level
Human trials will soon begin for a cancer vaccine
developed by Stanford researchers
BY PRIYA MENON to attack the tumour. However,
as the tumour grows, it devises
ways to suppress this activity of
the T-cells.
The new method reactivates T-
cells and harnesses a much stron-
ger immune response against
the tumour. It uses a combina-
tion of two molecules; the fi rst
is a short piece of DNA or the
CpG oligonucleotide causing
the T-cells to increase expression
of receptor molecules, OX40,
and the other is an antibody that
binds with the OX40, which
activates the T-cells to amplify
the anti-cancer response. Dr
Idit Sagiv-Barfi , the lead author
of the study, explains, “We use
a combination of two reagents.
The fi rst, CpG, is a small DNA
sequence that has properties of
microbial/bacterial DNA un-
like human DNA. When it is in-
jected into the tumour, immune
cells in the tumour sense it as
foreign DNA and begin a sig-
naling cascade eventually lead-
ing to a local immune response.
T-cells are among the cells that
are activated, as a result of this
activation they increase the ex-
pression of a protein known
as OX40 on their surface. The
DR IDIT SAGIV-BARFI
tumours in mice and found that
this could eliminate all traces of
cancer in the animals, including
distant, untreated metastases.
“When we use these two
agents together, we see the elim-
ination of tumours all over the
body,” said Ronald Levy, MD,
professor of oncology and se-
nior author of the study, in the
Stanford press release.
The cancer environment dis-
plays a strange kind of relation-
ship with the immune system.
Immune cells like T-cells rec-
ognise the abnormal proteins
present on the surface of can-
cer cells and infi ltrate the cells