Granulocyte/macrophage-colony-stimulating factor released by adenovirally transduced CT26 cells leads to the local expression of macrophage inflammatory protein 1α and accumulation of dendritic cells at vaccination sites in vivo
Granulocyte/macrophage-colony-stimulating factor released by adenovirally transduced CT26 cells leads to the local expression of macrophage inflammatory protein 1α and accumulation of dendritic cells at vaccination sites in vivo
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腺病毒转导的 CT26 细胞释放的粒细胞/巨噬细胞集落刺激因子导致巨噬细胞炎症蛋白 1α 的局部表达以及树突状细胞在体内疫苗接种部位的积累
DOI:
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发表时间:
1999
期刊:
影响因子:
--
通讯作者:
Tsuneo Suzuki
中科院分区:
文献类型:
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作者:
T. Kielian;E. Nagai;A. Ikubo;C. Rasmussen;Tsuneo Suzuki
Abstract Antigen presenting cells (APC) play an essential role in the generation of tumor-specific immune responses. Dendritic cells are the most potent of APC, capable of activating both antigen-specific CD4+ and CD8+ T cells. Previously, we have described how vaccination of mice with irradiated tumor cells producing granulocyte/macrophage-colony-stimulating factor (GM-CSF) induces tumor-specific immunity capable of protecting mice from a subsequent tumor challenge. The present study extends these findings to examine the types of APC infiltrating vaccination sites and the chemokines responsible for their recruitment. GM-CSF released from genetically engineered tumor cells led to the local accumulation of dendritic cells in and around the vaccination site. Quantification revealed a significant ten-fold increase in the number of dendritic cells infiltrating GM-CSF-producing as opposed to β-galactosidase-producing (control) vaccination sites. Reverse transcription/polymerase chain reaction, enzyme-linked immunosorbent assay, and immunohistochemical analysis of vaccination sites revealed that MIP-1α may be responsible for dendritic cell infiltration into GM-CSF-producing tissues. These findings suggest that GM-CSF may indirectly recruit dendritic cells into vaccination sites through the local production of MIP-1α.
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DOI:
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发表时间:
1997-03
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
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作者:
D. Gabrilovich;Jadranco Corak;I. Ciernik;D. Kavanaugh;D. Carbone
通讯作者:
D. Gabrilovich;Jadranco Corak;I. Ciernik;D. Kavanaugh;D. Carbone
影响因子:
4.3
作者:
Gabrilovich, DI;Ciernik, IF;Carbone, DP
通讯作者:
Carbone, DP
影响因子:
11.2
作者:
C. Armstrong;R. Botella;T. H. Galloway;Nancy B. Murray;Jill Kramp;I. S. Song;J. Ansel
通讯作者:
C. Armstrong;R. Botella;T. H. Galloway;Nancy B. Murray;Jill Kramp;I. S. Song;J. Ansel
DOI:
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发表时间:
1996
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Levitsky,HI;Montgomery,J;Ahmadzadeh,M;Staveley-O'Carroll,K;Guarnieri,F;Longo,DL;Kwak,LW
通讯作者:
Kwak,LW