Open AccessLow‐dose paclitaxel improves the therapeutic efficacy of recombinant adenovirus encoding CCL21 chemokine against murine cancer
Author(s) -
Chen Ping,
Luo Shan,
Wen YanJun,
Li YuHua,
Li Jiong,
Wang YongSheng,
Du LiCheng,
Zhang Ping,
Tang Jiao,
Yang DaBing,
Hu HuoZhen,
Zhao Xia,
Wei YuQuan
Publication year - 2014
Publication title -
cancer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 1347-9032
DOI - 10.1111/cas.12537
Subject(s) - paclitaxel , cancer research , chemokine , medicine , oncolytic virus , melanoma , immunotherapy , ccl21 , cd8 , adenoviridae , cancer , immunology , ccl17 , chemokine receptor , pharmacology , immune system , biology , genetic enhancement , biochemistry , gene
Secondary lymphoid tissue chemokine (SLC/CCL21), one of the CC chemokines, exerts potent antitumor immunity by co‐localizing T cells and dendritic cells at the tumor site and is currently tested against human solid tumors. Here, we investigated whether the combination of recombinant adenovirus encoding murine CCL21 (Ad‐ mCCL 21) with low‐dose paclitaxel would improve therapeutic efficacy against murine cancer. Immunocompetent mice bearing B16‐F10 melanoma or 4T1 breast carcinoma were treated with either Ad‐ mCCL 21, paclitaxel, or both agents together. Our results showed that Ad‐ mCCL 21 + low‐dose paclitaxel more effectively reduced the growth of tumors as compared with either treatment alone and significantly prolonged survival time of the tumor‐bearing animals. These antitumor effects of the combined therapy were linked to altered cytokine network at the tumor site, enhanced apoptosis of tumor cells, and decreased formation of new vessels in tumors. Importantly, the combined therapy elicited a strong therapeutic antitumor immunity, which could be partly abrogated by the depletion of CD4 + or CD8 + T lymphocytes. Collectively, these preclinical evaluations may provide a combined strategy for antitumor immunity and should be considered for testing in clinical trials.