共 54 条
IL-15 ex vivo overcomes CD4+ T cell deficiency for the induction of human antigen-specific CD8+ T cell responses
被引:8
作者:
Yu, Huifeng
[1
]
Tawab-Amiri, Abdul
[2
]
Dzutsev, Amiran
[1
]
Sabatino, Marianna
[2
]
Aleman, Karen
[3
]
Yarchoan, Robert
[3
]
Terabe, Masaki
[1
]
Sui, Yongjun
[1
]
Berzofsky, Jay A.
[1
]
机构:
[1] Natl Canc Inst, Vaccine Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[2] Natl Canc Inst, Ctr Clin, Dept Transfus Med, Bethesda, MD 20892 USA
[3] Natl Canc Inst, HIV & AIDS Malignancy Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
关键词:
primary cells;
dendritic cells;
lymphoid cell-mediated immunity;
MATURE DENDRITIC CELLS;
INTERLEUKIN-15;
HELP;
VACCINE;
MEMORY;
HIV;
INFECTION;
EXPANSION;
CYTOKINE;
LYMPHOCYTES;
D O I:
10.1189/jlb.1010579
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
CD4(+) Th cells are important for the induction and maintenance of antigen-specific CD8(+) T cell function, so their loss or dysfunction in HIV-infected or cancer patients could reduce the patients' ability to control viral infection. Previous work in murine systems indicated that IL-15 codelivered with vaccines could overcome CD4(+) Th cell deficiency for induction of functionally efficient CD8(+) T cells and maintenance of viral-specific CTLs, but its efficacy in helping primary human CD8(+) T cell responses is unknown. In the present study, a peptide-pulsed, DC-based human coculture ex vivo system was used to study the role of IL-15 in overcoming CD4(+) Th deficiency to elicit CD8(+) T cell responses in CD4-depleted PBMCs from healthy individuals and PBMCs from HIV-1-infected patients. We found that IL-15 could overcome CD4(+) Th deficiency to induce primary and recall memory CD8(+) T cell responses in healthy individuals. Moreover, in CD4-deficient, HIV-1-infected patients with diminished CD8(+) T cell responses, IL-15 greatly enhanced CD8(+) T cell responses to alloantigen. These results suggest that IL-15 may be useful in the development of therapeutic and preventive vaccines against cancers and viral infections in patients defective in CD4(+) Th cell. J. Leukoc. Biol. 90: 205-214; 2011.
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页码:205 / 214
页数:10
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