Abstract | AIM: Accumulating evidence has indicated that hyperthermia using magnetite nanoparticles induces antitumor immunity. This study investigated the diversity of T-cell receptors (TCRs) in tumor-infiltrating lymphocytes after hyperthermia using magnetite nanoparticles. MATERIALS & METHODS: Functionalized magnetite nanoparticles, N-propionyl-4-S-cysteaminylphenol (NPrCAP)/ magnetite, were synthesized by conjugating the melanogenesis substrate NPrCAP with magnetite nanoparticles. NPrCAP/magnetite nanoparticles were injected into B16 melanomas in C57BL/6 mice, which were subjected to an alternating magnetic field for hyperthermia treatment. RESULTS: Enlargement of the tumor-draining lymph nodes was observed after hyperthermia. The TCR repertoire was restricted in tumor-infiltrating lymphocytes, and expansion of Vβ11(+) T cells was preferentially found. DNA sequences of the third complementaritydetermining regions revealed the presence of clonally expanded T cells. CONCLUSION: These results indicate that the T-cell response in B16 melanomas after hyperthermia is dominated by T cells directed toward a limited number of epitopes and that epitope-specific T cells frequently use a restricted TCR repertoire.
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Authors | Akira Ito, Masaki Yamaguchi, Noriaki Okamoto, Yuji Sanematsu, Yoshinori Kawabe, Kazumasa Wakamatsu, Shosuke Ito, Hiroyuki Honda, Takeshi Kobayashi, Eiichi Nakayama, Yasuaki Tamura, Masae Okura, Toshiharu Yamashita, Kowichi Jimbow, Masamichi Kamihira |
Journal | Nanomedicine (London, England)
(Nanomedicine (Lond))
Vol. 8
Issue 6
Pg. 891-902
(Jun 2013)
ISSN: 1748-6963 [Electronic] England |
PMID | 23066648
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Magnetite Nanoparticles
- Receptors, Antigen, T-Cell
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Topics |
- Animals
- Female
- Hyperthermia, Induced
(methods)
- Lymph Nodes
(immunology, pathology)
- Lymphocytes, Tumor-Infiltrating
(immunology, pathology)
- Magnetic Fields
- Magnetite Nanoparticles
(chemistry, therapeutic use)
- Melanoma, Experimental
(immunology, pathology, therapy)
- Mice
- Mice, Inbred C57BL
- Receptors, Antigen, T-Cell
(immunology)
- T-Lymphocytes
(immunology, pathology)
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