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使用包被抗原的磁珠进行体外再刺激以灵敏检测抗原特异性T细胞。

Sensitive detection of antigen-specific T-cells using bead-bound antigen for in vitro re-stimulation.

作者信息

Bronge Mattias, Kaiser Andreas, Carvalho-Queiroz Claudia, Nilsson Ola B, Ruhrmann Sabrina, Holmgren Erik, Olsson Tomas, Gafvelin Guro, Grönlund Hans

机构信息

Therapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine L8:02, 171 76, Stockholm, Sweden.

Neuroimmunology Unit, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine L8:04, 171 76, Stockholm, Sweden.

出版信息

MethodsX. 2019 Jul 8;6:1635-1641. doi: 10.1016/j.mex.2019.07.004. eCollection 2019.

DOI:10.1016/j.mex.2019.07.004
PMID:31367530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6651840/
Abstract

Reliable and sensitive detection of antigen specific cells is essential in several fields of research, whether it concerns monitoring responses to infectious agents or exploring the auto-antigen repertoire in autoimmune diseases. Identification of these cells is however difficult, especially when the cells often are rare and methods not sensitive, specific or practical enough. We propose a novel method of processing antigens before stimulation of cells which consists of covalently binding protein antigen to superparamagnetic micro-beads and using denaturing washes to remove contaminants. Peripheral blood mononuclear cells (PBMCs) from healthy donors were stimulated using both cytomegalovirus and tetanus-diphtheria antigen-beads as well as non-antigenic protein-beads as negative control in an IFNγ FluoroSpot assay in order to detect Th1 and CD8 responses. The responses toward the antigen beads were both antigen specific and sensitive, with a detection threshold of 1 IFNγ producing T-cell per 18,000 PBMCs. •Covalently binding antigen to paramagnetic beads allows for harsh denaturing washes without loss of antigen.•Microbeads are phagocytosed by antigen presenting cells, resulting in efficient uptake, processing and presentation of the antigens.•The method allows the usage of relatively impure starting antigen material and whole PBMC samples without high background levels in follow up cellular assays.

摘要

在多个研究领域中,可靠且灵敏地检测抗原特异性细胞至关重要,无论是监测对感染因子的反应还是探索自身免疫性疾病中的自身抗原库。然而,识别这些细胞很困难,尤其是当这些细胞通常很稀少且检测方法不够灵敏、特异或实用时。我们提出了一种在刺激细胞之前处理抗原的新方法,该方法包括将蛋白质抗原共价结合到超顺磁性微珠上,并使用变性洗涤去除污染物。在IFNγ荧光斑点试验中,使用巨细胞病毒和破伤风 - 白喉抗原微珠以及非抗原性蛋白质微珠作为阴性对照,刺激健康供体的外周血单核细胞(PBMC),以检测Th1和CD8反应。对抗原微珠的反应具有抗原特异性且灵敏,检测阈值为每18,000个PBMC中有1个产生IFNγ的T细胞。

• 将抗原共价结合到顺磁性微珠上可进行严苛的变性洗涤而不会损失抗原。

• 微珠被抗原呈递细胞吞噬,从而实现抗原的有效摄取、加工和呈递。

• 该方法允许使用相对不纯的起始抗原材料和完整的PBMC样品,且在后续细胞检测中不会产生高背景水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/d362ade31c2f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/0caad46bd4d6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/2b4897e4fe78/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/68a9238908c7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/41a196c1f7f8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/d362ade31c2f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/0caad46bd4d6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/2b4897e4fe78/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/68a9238908c7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/41a196c1f7f8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1b/6651840/d362ade31c2f/gr4.jpg

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