Polyfunctionality of a DKK1 self-antigen-specific CD8+ T lymphocyte clone in lung cancer

被引:2
作者
Forget, Marie-Andree [1 ,2 ]
Reuben, Alexandre [1 ,2 ]
Turcotte, Simon [1 ,2 ]
Martin, Jocelyne [3 ]
Lapointe, Rejean [1 ,2 ]
机构
[1] Univ Montreal, Dept Med, Hop Notre Dame de Bon Secours, Ctr Rech,Ctr Hosp Univ Montreal CRCHUM, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Inst Canc Montreal, Montreal, PQ H2L 4M1, Canada
[3] CHUM, Hop Notre Dame de Bon Secours, Dept Surg, Div Thorac Surg, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
Dickkopf-1 (DKK1); Polyfunctionality; Lung cancer; CD8(+) T lymphocyte; TUMOR; CELLS; MULTIFUNCTIONALITY; IMMUNIZATION; EXPRESSION; VACCINE;
D O I
10.1007/s00262-011-1055-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Polyfunctionality is the capacity of a T-cell to execute a variety of effector functions mainly mediated by production of cytokines, chemokines, and cytolytic enzymes. Studies in anti-viral immunity have acknowledged the importance of polyfunctionality in the clearance of infections and maintenance of protection. Although accepted in the field, this concept has not been as well characterized in cancer immunology. Here, we report the polyfunctionality profile analysis of a CD8(+) T-cell clone isolated from a lung cancer patient and directed against Dickkopf-1, a potentially new tumor-associated antigen (TAA). The clone showed Tc1/Th1 effector tendencies confirmed by secretion of cytokines such as IFN-gamma, IP-10, MIP-1 beta, MIP-1 alpha, IL-2, GM-CSF, and expression of cytolytic enzyme granzyme B. This secretion profile is of particular interest in the context of an anti-tumor response. Although secretion of IL-5 and IL-13 was also detected, absence of IL-4 and IL-10 opposes the idea of cytokine-dependent Th1 inhibition. Establishing a comprehensive cytokine secretion profile may help predict T cells' specific response against a novel TAA in a peptide vaccination context. It may further help in selecting clones with an optimal functional profile from the peripheral blood of cancer patients for expansion and adoptive cell transfer therapy.
引用
收藏
页码:1119 / 1125
页数:7
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