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CD1介导的树突状细胞γ/δ T细胞成熟

CD1-mediated gamma/delta T cell maturation of dendritic cells.

作者信息

Leslie David S, Vincent Michael S, Spada Franca M, Das Hiranmoy, Sugita Masahiko, Morita Craig T, Brenner Michael B

机构信息

Division of Rheumatology, Immunology and Allergy, Department of Medicine, Brigham and Women's Hospital at Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Exp Med. 2002 Dec 16;196(12):1575-84. doi: 10.1084/jem.20021515.

DOI:10.1084/jem.20021515
PMID:12486100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2196072/
Abstract

Immature myeloid dendritic cells (DCs) express only low levels of major histocompatibility complex (MHC) class II but express high levels of CD1 a, b, and c antigen-presenting molecules at the cell surface. As Vdelta1+ gamma/delta T cells are the main tissue subset of gamma/delta T cells and they are known to recognize CD1c in the absence of specific foreign antigen recognition, we examined the possible interaction of these T cells with immature DCs. We show that CD1-restricted gamma/delta T cells can mediate the maturation of DCs. DC maturation required cell-cell contact and could be blocked by antibodies against CD1c. The maturation process was partially mediated by tumor necrosis factor alpha. Importantly, immature DCs matured in the presence of lipopolysaccharide and CD1-restricted gamma/delta T cells produced bioactive interleukin-12p70. In addition, these DCs were able to efficiently present peptide antigens to naive CD4+ T cells. CD1-restricted gamma/delta T cell recognition of immature DCs provides the human immune system with the capacity to rapidly generate a pool of mature DCs early during microbial invasion. This may be an important source of critical host signals for T helper type 1 polarization of antigen-specific naive T cells and the subsequent adaptive immune response.

摘要

未成熟髓样树突状细胞(DCs)仅低水平表达主要组织相容性复合体(MHC)II类分子,但在细胞表面高水平表达CD1a、b和c抗原呈递分子。由于Vδ1 + γ/δ T细胞是γ/δ T细胞的主要组织亚群,并且已知它们在缺乏特异性外来抗原识别的情况下可识别CD1c,因此我们研究了这些T细胞与未成熟DCs之间可能的相互作用。我们发现,CD1限制性γ/δ T细胞可介导DCs的成熟。DC成熟需要细胞间接触,并且可被抗CD1c抗体阻断。成熟过程部分由肿瘤坏死因子α介导。重要的是,在脂多糖存在下成熟的未成熟DCs以及CD1限制性γ/δ T细胞可产生具有生物活性的白细胞介素-12p70。此外,这些DCs能够有效地将肽抗原呈递给初始CD4 + T细胞。未成熟DCs的CD1限制性γ/δ T细胞识别为人类免疫系统提供了在微生物入侵早期快速产生成熟DCs池的能力。这可能是抗原特异性初始T细胞向1型辅助性T细胞极化以及随后的适应性免疫反应的关键宿主信号的重要来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94c9/2196072/a291b1d311e8/20021515f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94c9/2196072/1e83d14ae583/20021515f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94c9/2196072/a291b1d311e8/20021515f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94c9/2196072/1e83d14ae583/20021515f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94c9/2196072/a291b1d311e8/20021515f2.jpg

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