OMIP-111: Immune-Profiling of T Helper 1 (Th1), Th2, and Th17 Signatures in Murine Splenocytes by Targeting Intracellular Cytokines

被引:0
作者
Barman, Soumik [1 ,2 ]
Kelly, Aisling [1 ]
Dong, Danica [1 ]
Patel, Arsh [3 ]
Buonopane, Michael J. [3 ]
Gonzales, Jake [4 ]
Janoschek, Ben [5 ]
Draghi II, Andrew [5 ]
Dowling, David J. [1 ,2 ]
机构
[1] Boston Childrens Hosp, Precis Vaccines Program, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Cytometry Cores, Boston, MA USA
[4] BioLegend Inc, San Diego, CA USA
[5] Sony Biotechnol Inc, San Jose, CA USA
关键词
murine splenocytes; spectral flow cytometry; Th1; cells; Th2; Th17; mitogen; murine T cells; Sony ID7000; CELLS;
D O I
10.1002/cyto.a.24926
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Functional cytokines shape both innate and adaptive immune responses in the host after infection or immunization. Deep immunophenotyping of the key functional cytokine signatures associated with T cells in murine lymphoid tissue, especially in the spleen, is challenging. Using spectral flow cytometry, we developed a 17-parameter panel to profile major immune cell subsets along with T cells, memory phenotypes, and functional cytokines in murine splenocytes in steady state as well as in stimulated conditions. This panel dissects the memory T cell compartment via CD62L and CD44 expression after mitogen stimulation. To profile T helper (Th) cell distribution after mitogen stimulation, established Th1 markers IFN gamma, TNF, and IL-2; Th2 markers IL-4/5; and the Th17 marker, IL-17, are included. This optimized multicolor spectral flow panel allows a detailed immune-profiling of functional cytokines in the murine T cell compartment and might be useful for exploratory analysis of how these functional cytokines shape host immunity after infection or vaccination. Our panel could be easily modified if researchers wish to tailor the panel to their specific needs.
引用
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页数:5
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