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健康供体中针对因子VIII的CD4 T细胞高频存在,且包括初始细胞和记忆细胞。

CD4 T cells specific for factor VIII are present at high frequency in healthy donors and comprise naïve and memory cells.

作者信息

Meunier Sylvain, Menier Catherine, Marcon Elodie, Lacroix-Desmazes Sébastien, Maillère Bernard

机构信息

CEA-Saclay, Institute Frederic Joliot, Service d'Ingénierie Moléculaire des Protéines, Gif-sur-Yvette, France; and.

INSERM Unité Mixte de Recherche S 1138, Centre de Recherche des Cordeliers, Paris, France.

出版信息

Blood Adv. 2017 Sep 25;1(21):1842-1847. doi: 10.1182/bloodadvances.2017008706. eCollection 2017 Sep 26.

DOI:10.1182/bloodadvances.2017008706
PMID:29296830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5728100/
Abstract

We investigated the frequency and subset origin of circulating factor VIII (FVIII)-specific CD4 T cells in healthy donors. Total CD4 T cells and purified CD4 T-cell subsets were stimulated with FVIII-loaded autologous dendritic cells and challenged for specificity in interferon-γ enzyme-linked immunospots. The number of specific T-cell lines allowed estimation of the frequency of T cells circulating in the blood of the donors. All the 16 healthy donors generated strong in vitro T-cell responses, leading to the generation of 154 FVIII-specific T-cell lines. The mean frequency of FVIII-specific CD4 T cells in healthy donors was similar to that of T cells specific for foreign antigens and greater than that of T cells specific for known immunogenic therapeutic proteins. Normal levels of endogenous FVIII in healthy donors therefore do not prevent a significant escape of FVIII-specific CD4 T cells from negative thymic selection. FVIII-specific T cells mainly originated from both the naïve and central memory cell subsets, but their frequencies remained low as compared with those of cells specific for foreign antigens in immunized donors. The observation of a spontaneous generation of FVIII-specific memory T cells without a global expansion suggests peculiar peripheral tolerance mechanisms to FVIII in healthy donors.

摘要

我们研究了健康供体中循环的凝血因子VIII(FVIII)特异性CD4 T细胞的频率和亚群来源。用负载FVIII的自体树突状细胞刺激总CD4 T细胞和纯化的CD4 T细胞亚群,并在干扰素-γ酶联免疫斑点试验中检测其特异性。通过特异性T细胞系的数量可估计供体血液中循环T细胞的频率。所有16名健康供体均产生了强烈的体外T细胞应答,共产生了154个FVIII特异性T细胞系。健康供体中FVIII特异性CD4 T细胞的平均频率与针对外来抗原的T细胞相似,且高于针对已知免疫原性治疗蛋白的T细胞。因此,健康供体中内源性FVIII的正常水平并不能阻止FVIII特异性CD4 T细胞从阴性胸腺选择中显著逃逸。FVIII特异性T细胞主要来源于初始和中枢记忆细胞亚群,但与免疫供体中针对外来抗原的细胞相比,其频率仍然较低。在没有整体扩增的情况下自发产生FVIII特异性记忆T细胞这一现象表明,健康供体中存在针对FVIII的特殊外周耐受机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/997c/5728100/084c43533479/advances008706absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/997c/5728100/084c43533479/advances008706absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/997c/5728100/084c43533479/advances008706absf1.jpg

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本文引用的文献

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The Contained Self-Reactive Peripheral T Cell Repertoire: Size, Diversity, and Cellular Composition.受限的自身反应性外周T细胞库:大小、多样性和细胞组成。
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The Tumor Antigen Cyclin B1 Hosts Multiple CD4 T Cell Epitopes Differently Recognized by Pre-Existing Naive and Memory Cells in Both Healthy and Cancer Donors.
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Acquired hemophilia A (AHA) due to anti-SARS-CoV-2 vaccination: A systematic review.抗SARS-CoV-2疫苗接种所致获得性甲型血友病(AHA):一项系统评价。
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