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在鼠皮肤移植物抗宿主病中 T 细胞的体内动力学及其与树突状细胞的相互作用。

In vivo dynamics of T cells and their interactions with dendritic cells in mouse cutaneous graft-versus-host disease.

机构信息

Division of Hematology, Department of Oncology, Hôpitaux Universitaires de Genève, Geneva, Switzerland.

Department of Medicine, University of Texas Southwestern, Dallas, TX.

出版信息

Blood Adv. 2019 Jul 23;3(14):2082-2092. doi: 10.1182/bloodadvances.2019000227.

Abstract

Graft-versus-host disease (GVHD) is a major cause of morbidity and mortality in allogeneic hematopoietic stem cell transplantation (alloSCT). By static microscopy, cutaneous GVHD lesions contain a mix of T cells and myeloid cells. We used 2-photon intravital microscopy to investigate the dynamics of CD4 and CD8 T cells and donor dendritic cells (DCs) in cutaneous GVHD lesions in an MHC-matched, multiple minor histocompatibility antigen-mismatched (miHA) model. The majority of CD4 and CD8 cells were stationary, and few cells entered and stopped or were stopped and left the imaged volumes. CD8 cells made TCR:MHCI-dependent interactions with CD11c cells, as measured by the durations that CD8 cells contacted MHCI vs MHCI DCs. The acute deletion of LangerinCD103 DCs, which were relatively rare, did not affect CD8 cell motility and DC contact times, indicating that LangerinCD103 DCs provide stop signals to CD8 cells. CD4 cells, in contrast, had similar contact durations with MHCII and MHCII DCs. However, CD4 motility rapidly increased after the infusion of an MHCII-blocking antibody, indicating that TCR signaling actively suppressed CD4 movements. Many CD4 cells still were stationary after anti-MHCII antibody infusion, suggesting CD4 cell heterogeneity within the lesion. These data support a model of local GVHD maintenance within target tissues.

摘要

移植物抗宿主病(GVHD)是异基因造血干细胞移植(alloSCT)中发病率和死亡率的主要原因。通过静态显微镜观察,皮肤 GVHD 病变包含 T 细胞和髓样细胞的混合物。我们使用双光子活体显微镜在 MHC 匹配、多个次要组织相容性抗原不匹配(miHA)模型中研究皮肤 GVHD 病变中 CD4 和 CD8 T 细胞和供体树突状细胞(DC)的动力学。大多数 CD4 和 CD8 细胞处于静止状态,很少有细胞进入并停止或停止并离开成像体积。CD8 细胞与 CD11c 细胞进行 TCR:MHCI 依赖性相互作用,这是通过 CD8 细胞与 MHCI 相比与 MHCI DC 接触的持续时间来衡量的。相对较少的 LangerinCD103 DC 的急性缺失不会影响 CD8 细胞的迁移率和 DC 接触时间,表明 LangerinCD103 DC 向 CD8 细胞提供停止信号。相比之下,CD4 细胞与 MHCII 和 MHCII DC 具有相似的接触持续时间。然而,在输注 MHCII 阻断抗体后,CD4 细胞的迁移率迅速增加,表明 TCR 信号积极抑制 CD4 运动。许多 CD4 细胞在抗 MHCII 抗体输注后仍然处于静止状态,这表明病变内 CD4 细胞存在异质性。这些数据支持局部 GVHD 在靶组织内维持的模型。

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