Abstract | BACKGROUND AND OBJECTIVE: DESIGN AND SETTING: Animal study conducted in the First Affiliated Hospital of Xi'an Jiaotong University from January 2009 to January 2010. PATIENTS AND METHODS:
Lymphopenia was induced by cyclophosphamide. A reconstituted immune system with different syngeneic lymphocytes was employed, including lymphocytes from naïve rats (unsensitized group), tumor-bearing rats ( tumor-bearing group), and tumor-bearing rats activated in vitro (activated group). All rats were immunized with granulocyte-macrophage colony-stimulating factor ( GM-CSF)-modified NuTu-19 ovarian cancer ( GM-CSF/NuTu-19) cells. Tumor vaccine-draining lymph nodes (TVDLNs) were harvested, and then stimulated to induce effector T cells (T(E)). T(E) were then adoptively transferred to rats bearing a 3-day pre-established abdominal tumor (NuTu-19), and the survival rate was calculated. RESULTS: Compared with the unsensitized group, the levels of interleukin-2 (IL-2) were significantly lower in the tumor-bearing group, whereas that of IL-4 were significantly higher (P<.05). The number of CD4+ T cells secreting interferon-γ and the specific cytotoxicity of CD8+ cytotoxic T lymphocytes were significantly lower (P<.05). The survival was significantly higher in the activated group compared with the other groups. CONCLUSIONS: Lymphocytes from tumor-bearing rats activated in vitro can effectively reverse the immunosuppressive effects of tumor-bearing hosts.
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Authors | Qi-ling Li, Shang-feng Gao, Yun-ping Wang, Jun Ma, Cai-xia Feng, Ying Wang, Yue-ling Wang |
Journal | Annals of Saudi medicine
(Ann Saudi Med)
2012 Mar-Apr
Vol. 32
Issue 2
Pg. 162-8
ISSN: 0975-4466 [Electronic] Saudi Arabia |
PMID | 22366830
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cancer Vaccines
- Cytokines
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Topics |
- Animals
- Cancer Vaccines
(immunology)
- Cytokines
(immunology)
- Female
- Immunotherapy, Adoptive
(methods)
- Lymphocytes, Tumor-Infiltrating
(immunology)
- Lymphopenia
(immunology, therapy)
- Ovarian Neoplasms
(immunology, therapy)
- Rats
- T-Lymphocytes
(immunology)
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