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用与MITD融合的抗原mRNA转染的永生化B细胞(IBMAM):抗原特异性T细胞扩增和TCR验证的有效工具。

Immortalized B Cells Transfected with mRNA of Antigen Fused to MITD (IBMAM): An Effective Tool for Antigen-Specific T-Cell Expansion and TCR Validation.

作者信息

Wang Zhe, Zhang Tiantian, Anderson Aaron, Lee Vincent, Szymura Szymon, Dong Zhenyuan, Kuang Benjamin, Oh Elizabeth, Liu Jingwei, Neelapu Sattva S, Kwak Larry, Cha Soung-Chul

机构信息

Toni Stephenson Lymphoma Center, Hematologic Malignancies Research Institute, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.

Department of Lymphoma and Myeloma, Division of Cancer Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Biomedicines. 2023 Mar 6;11(3):796. doi: 10.3390/biomedicines11030796.

Abstract

Peripheral mononuclear blood cells (PBMCs) are the most widely used study materials for immunomonitoring and antigen-specific T-cell identification. However, limited patient PBMCs and low-frequency antigen-specific T cells remain as significant technical challenges. To address these limitations, we established a novel platform comprised of optimized HLA-matched immortalized B cells transfected with mRNA of a prototype viral or tumor antigen conjugated to MHC class-I trafficking domain protein (MITD) to increase the efficiency of epitope expression in antigen-presenting cells (APCs) essential to expanding antigen-specific T cells. When applied to CMV as a model, the IBMAM platform could successfully expand CMV-specific T cells from low-frequency CMV PBMCs from seropositive donors. Additionally, this platform can be applied to the validation of antigen specific TCRs. Together, compared to using APCs with synthesized peptides, this platform is an unlimited, highly efficient, and cost-effective resource in detecting and expanding antigen-specific T cells and validating antigen-specific TCRs.

摘要

外周血单个核细胞(PBMC)是免疫监测和抗原特异性T细胞鉴定中使用最广泛的研究材料。然而,患者PBMC数量有限以及抗原特异性T细胞频率较低仍然是重大的技术挑战。为了解决这些限制,我们建立了一个新型平台,该平台由经过优化的、与I类主要组织相容性复合体(MHC)转运结构域蛋白(MITD)偶联的原型病毒或肿瘤抗原的mRNA转染的HLA匹配永生化B细胞组成,以提高抗原呈递细胞(APC)中表位表达的效率,这对于扩增抗原特异性T细胞至关重要。当将其应用于巨细胞病毒(CMV)作为模型时,IBMAM平台可以成功地从血清阳性供体的低频CMV PBMC中扩增出CMV特异性T细胞。此外,该平台可应用于抗原特异性T细胞受体(TCR)的验证。总体而言,与使用合成肽的APC相比,该平台在检测和扩增抗原特异性T细胞以及验证抗原特异性TCR方面是一种无限、高效且具有成本效益的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee46/10045729/0a6e765acb34/biomedicines-11-00796-g001.jpg

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