Improved Multiplex Immunohistochemistry for Immune Microenvironment Evaluation of Mouse Formalin-Fixed, Paraffin-Embedded Tissues

被引:38
作者
Sorrelle, Noah [1 ]
Ganguly, Debolina [1 ]
Dominguez, Adrian T. A. [1 ]
Zhang, Yuqing [1 ]
Huang, Huocong [1 ]
Dahal, Lekh N. [2 ]
Burton, Natalie [1 ]
Ziemys, Arturas [3 ]
Brekken, Rolf A. [1 ,4 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Div Surg Oncol, Dept Surg, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75390 USA
[2] Univ Southampton, Southampton Gen Hosp, Ctr Canc Immunol, Fac Med, Southampton 016 6YD, Hants, England
[3] Houston Methodist Res Inst, Dept Nanomed, Houston, TX 77030 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
ANTIGEN-RETRIEVAL; CELLS; MACROPHAGES; PROGRESSION; INHIBITION; EXPRESSION; SPLEEN; CANCER;
D O I
10.4049/jimmunol.1800878
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune profiling of tissue through multiplex immunohistochemistry is important for the investigation of immune cell dynamics, and it can contribute to disease prognosis and evaluation of treatment response in cancer patients. However, protocols for mouse formalin-fixed, paraffin-embedded tissue have been less successful. Given that formalin fixation and paraffin embedding remains the most common preparation method for processing mouse tissue, this has limited the options to study the immune system and the impact of novel therapeutics in preclinical models. In an attempt to address this, we developed an improved immunohistochemistry protocol with a more effective Ag-retrieval buffer. We also validated 22 Abs specific for mouse immune cell markers to distinguish B cells, T cells, NK cells, macrophages, dendritic cells, and neutrophils. In addition, we designed and tested novel strategies to identify immune cells for which unique Abs are currently not available. Last, in the 4T1 model of breast cancer, we demonstrate the utility of our protocol and Ab panels in the quantitation and spatial distribution of immune cells.
引用
收藏
页码:292 / 299
页数:8
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