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白细胞介素-7通过作用于宿主细胞来调节抗肿瘤CD8 + T细胞反应。

Interleukin-7 Modulates Anti-Tumor CD8+ T Cell Responses via Its Action on Host Cells.

作者信息

Deiser Katrin, Stoycheva Diana, Bank Ute, Blankenstein Thomas, Schüler Thomas

机构信息

Institute of Molecular and Clinical Immunology, Medical Faculty, Otto-von-Guericke University, 39120 Magdeburg, Germany.

Institute of Immunology, Charité-Universitaetsmedizin Berlin, Campus Benjamin Franklin, 12200 Berlin, Germany.

出版信息

PLoS One. 2016 Jul 22;11(7):e0159690. doi: 10.1371/journal.pone.0159690. eCollection 2016.

Abstract

The adoptive transfer of antigen-specific CD8+ T cells is a promising approach for the treatment of chronic viral and malignant diseases. In order to improve adoptive T cell therapy (ATT) of cancer, recent strategies aim at the antibody-based blockade of immunosuppressive signaling pathways in CD8+ T cells. Alternatively, adjuvant effects of immunostimulatory cytokines might be exploited to improve therapeutic CD8+ T cell responses. For example, Interleukin-7 (IL-7) is a potent growth, activation and survival factor for CD8+ T cells that can be used to improve virus- and tumor-specific CD8+ T cell responses. Although direct IL-7 effects on CD8+ T cells were studied extensively in numerous models, the contribution of IL-7 receptor-competent (IL-7R+) host cells remained unclear. In the current study we provide evidence that CD8+ T cell-mediated tumor rejection in response to recombinant IL-7 (rIL-7) therapy is strictly dependent on IL-7R+ host cells. On the contrary, CD8+ T cell expansion is independent of host IL-7R expression. If, however, rIL-7 therapy and peptide vaccination are combined, host IL-7R signaling is crucial for CD8+ T cell expansion. Unexpectedly, maximum CD8+ T cell expansion relies mainly on IL-7R signaling in non-hematopoietic host cells, similar to the massive accumulation of dendritic cells and granulocytes. In summary, we provide evidence that IL-7R+ host cells are major targets of rIL-7 that modulate therapeutic CD8+ T cell responses and the outcome of rIL-7-assisted ATT. This knowledge may have important implications for the design and optimization of clinical ATT protocols.

摘要

抗原特异性CD8+ T细胞的过继性转移是治疗慢性病毒性疾病和恶性疾病的一种很有前景的方法。为了改善癌症的过继性T细胞疗法(ATT),最近的策略旨在基于抗体阻断CD8+ T细胞中的免疫抑制信号通路。另外,可以利用免疫刺激细胞因子的佐剂作用来改善治疗性CD8+ T细胞反应。例如,白细胞介素-7(IL-7)是CD8+ T细胞的一种有效的生长、激活和存活因子,可用于改善病毒特异性和肿瘤特异性CD8+ T细胞反应。尽管在众多模型中对IL-7对CD8+ T细胞的直接作用进行了广泛研究,但具有IL-7受体活性(IL-7R+)的宿主细胞的作用仍不清楚。在本研究中,我们提供证据表明,重组IL-7(rIL-7)治疗引起的CD8+ T细胞介导的肿瘤排斥反应严格依赖于IL-7R+宿主细胞。相反,CD8+ T细胞的扩增不依赖于宿主IL-7R的表达。然而,如果将rIL-7治疗与肽疫苗接种相结合,宿主IL-7R信号传导对于CD8+ T细胞的扩增至关重要。出乎意料的是,最大程度的CD8+ T细胞扩增主要依赖于非造血宿主细胞中的IL-7R信号传导,这与树突状细胞和粒细胞的大量积聚类似。总之,我们提供证据表明,IL-7R+宿主细胞是rIL-7的主要靶标,可调节治疗性CD8+ T细胞反应以及rIL-7辅助的ATT的结果。这一知识可能对临床ATT方案的设计和优化具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/715f/4957759/016d7186267a/pone.0159690.g001.jpg

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