TY - JOUR
T1 - Leveraging the immune system during chemotherapy
T2 - Moving calreticulin to the cell surface converts apoptotic death from "silent" to immunogenic
AU - Obeid, Michel
AU - Panaretakis, Theocharis
AU - Tesniere, Antoine
AU - Joza, Nick
AU - Tufi, Roberta
AU - Apetoh, Lionel
AU - Ghiringhelli, François
AU - Zitvogel, Laurence
AU - Kroemer, Guido
PY - 2007/9/1
Y1 - 2007/9/1
N2 - In contrast to prior belief, tumor cell apoptosis is not necessarily silent but can be immunogenic. By tracing how anthracyclines and γ-irradiation trigger immunogenic cell deaths, we found that they were causally connected to the exposure of calreticulin on the tumor cell surface, before apoptosis in the tumor cell itself occurred. Furthermore, we showed that calreticulin exposure was necessary and sufficient to increase proimmunogenic killing by other chemotherapies. Our findings suggest that calreticulin could serve as a biomarker to predict therapy-associated immune responses, and that tactics to expose calreticulin might improve the clinical efficacy of many cancer therapies.
AB - In contrast to prior belief, tumor cell apoptosis is not necessarily silent but can be immunogenic. By tracing how anthracyclines and γ-irradiation trigger immunogenic cell deaths, we found that they were causally connected to the exposure of calreticulin on the tumor cell surface, before apoptosis in the tumor cell itself occurred. Furthermore, we showed that calreticulin exposure was necessary and sufficient to increase proimmunogenic killing by other chemotherapies. Our findings suggest that calreticulin could serve as a biomarker to predict therapy-associated immune responses, and that tactics to expose calreticulin might improve the clinical efficacy of many cancer therapies.
UR - http://www.scopus.com/inward/record.url?scp=34548570079&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-07-1622
DO - 10.1158/0008-5472.CAN-07-1622
M3 - Review article
C2 - 17804698
AN - SCOPUS:34548570079
SN - 0008-5472
VL - 67
SP - 7941
EP - 7944
JO - Cancer Research
JF - Cancer Research
IS - 17
ER -