TY - JOUR
T1 - Local radiation therapy inhibits tumor growth through the generation of tumor-specific CTL
T2 - Its potentiation by combination with TH1 cell therapy
AU - Takeshima, Tsuguhide
AU - Chamoto, Kenji
AU - Wakita, Daiko
AU - Ohkuri, Takayuki
AU - Togashi, Yuji
AU - Shirato, Hiroki
AU - Kitamura, Hidemitsu
AU - Nishimura, Takashi
PY - 2010/4/1
Y1 - 2010/4/1
N2 - Radiation therapy is one of the primary treatment modalities for cancer along with chemotherapy and surgical therapy. The main mechanism of the tumor reduction after irradiation has been considered to be damage to the tumor DNA. However, we found that tumor-specific CTL, which were induced in the draining lymph nodes (DLN) and tumor tissue of tumor-bearing mice, play a crucial role in the inhibition of tumor growth by radiation. Indeed, the therapeutic effect of irradiation was almost completely abolished in tumor-bearing mice by depleting CD8+ T cells through anti-CD8 monoclonal antibody administration. In mice whose DLN were surgically ablated or genetically defective (Aly/Aly mice), the generation of tetramer+ tumor-specific CTL at the tumor site was greatly reduced in parallel with the attenuation of the radiation-induced therapeutic effect against the tumor. This indicates that DLN are essential for the activation and accumulation of radiationinduced CTL, which are essential for inhibition of the tumor. A combined therapy of local radiation with ThI cell therapy augmented the generation of tumor-specific CTL at the tumor site and induced a complete regression of the tumor, although radiation therapy alone did not exhibit such a pronounced therapeutic effect. Thus, we conclude that the combination treatment of local radiation therapy and Th1 cell therapy is a rational strategy to augment antitumor activity mediated by tumor-specific CTL.
AB - Radiation therapy is one of the primary treatment modalities for cancer along with chemotherapy and surgical therapy. The main mechanism of the tumor reduction after irradiation has been considered to be damage to the tumor DNA. However, we found that tumor-specific CTL, which were induced in the draining lymph nodes (DLN) and tumor tissue of tumor-bearing mice, play a crucial role in the inhibition of tumor growth by radiation. Indeed, the therapeutic effect of irradiation was almost completely abolished in tumor-bearing mice by depleting CD8+ T cells through anti-CD8 monoclonal antibody administration. In mice whose DLN were surgically ablated or genetically defective (Aly/Aly mice), the generation of tetramer+ tumor-specific CTL at the tumor site was greatly reduced in parallel with the attenuation of the radiation-induced therapeutic effect against the tumor. This indicates that DLN are essential for the activation and accumulation of radiationinduced CTL, which are essential for inhibition of the tumor. A combined therapy of local radiation with ThI cell therapy augmented the generation of tumor-specific CTL at the tumor site and induced a complete regression of the tumor, although radiation therapy alone did not exhibit such a pronounced therapeutic effect. Thus, we conclude that the combination treatment of local radiation therapy and Th1 cell therapy is a rational strategy to augment antitumor activity mediated by tumor-specific CTL.
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U2 - 10.1158/0008-5472.CAN-09-2982
DO - 10.1158/0008-5472.CAN-09-2982
M3 - Article
C2 - 20215523
AN - SCOPUS:77950829391
SN - 0008-5472
VL - 70
SP - 2697
EP - 2706
JO - Cancer Research
JF - Cancer Research
IS - 7
ER -