Detecting Antigen-Specific T Cell Responses: From Bulk Populations to Single Cells
被引:27
|
作者:
Phetsouphanh, Chansavath
论文数: 0引用数: 0
h-index: 0
机构:
Univ New S Wales, Kirby Inst, Sydney, NSW 2031, AustraliaUniv New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
Phetsouphanh, Chansavath
[1
]
Zaunders, John James
论文数: 0引用数: 0
h-index: 0
机构:
Univ New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
St Vincents Hosp, Ctr Appl Med Res, Sydney, NSW 2010, AustraliaUniv New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
Zaunders, John James
[1
,2
]
Kelleher, Anthony Dominic
论文数: 0引用数: 0
h-index: 0
机构:
Univ New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
St Vincents Hosp, Ctr Appl Med Res, Sydney, NSW 2010, AustraliaUniv New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
Kelleher, Anthony Dominic
[1
,2
]
机构:
[1] Univ New S Wales, Kirby Inst, Sydney, NSW 2031, Australia
[2] St Vincents Hosp, Ctr Appl Med Res, Sydney, NSW 2010, Australia
来源:
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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2015年
/
16卷
/
08期
基金:
澳大利亚国家健康与医学研究理事会;
关键词:
antigen-specific T cells;
digital PCR;
microfluidics;
mingle-cell RNA-seq;
FLUORESCENT DYES;
MASS CYTOMETRY;
FLOW-CYTOMETRY;
CENTRAL MEMORY;
ELISPOT ASSAY;
CD4(+);
IMMUNE;
HETEROGENEITY;
EFFECTOR;
EXPRESSION;
D O I:
10.3390/ijms160818878
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
A new generation of sensitive T cell-based assays facilitates the direct quantitation and characterization of antigen-specific T cell responses. Single-cell analyses have focused on measuring the quality and breadth of a response. Accumulating data from these studies demonstrate that there is considerable, previously-unrecognized, heterogeneity. Standard assays, such as the ICS, are often insufficient for characterization of rare subsets of cells. Enhanced flow cytometry with imaging capabilities enables the determination of cell morphology, as well as the spatial localization of the protein molecules within a single cell. Advances in both microfluidics and digital PCR have improved the efficiency of single-cell sorting and allowed multiplexed gene detection at the single-cell level. Delving further into the transcriptome of single-cells using RNA-seq is likely to reveal the fine-specificity of cellular events such as alternative splicing (i.e., splice variants) and allele-specific expression, and will also define the roles of new genes. Finally, detailed analysis of clonally related antigen-specific T cells using single-cell TCR RNA-seq will provide information on pathways of differentiation of memory T cells. With these state of the art technologies the transcriptomics and genomics of Ag-specific T cells can be more definitively elucidated.
机构:
Howard Hughes Med Inst, Dept Microbiol & Immunol, Stanford, CA USA
Howard Hughes Med Inst, Inst Immun Transplantat & Infect, Stanford, CA USA
Howard Hughes Med Inst, Stanford, CA USAASTAR, Singapore Immunol Network SIgN, Singapore, Singapore