Quantitative Multiplex Immunohistochemistry Reveals Myeloid-Inflamed Tumor-Immune Complexity Associated with Poor Prognosis

Takahiro Tsujikawa(Oregon Health & Science University), Sushil Kumar(Oregon Health & Science University), Rohan N. Borkar(Intel (United States)), Vahid Azimi(Intel (United States)), Guillaume Thibault(Oregon Health & Science University), Young Hwan Chang(Oregon Health & Science University), Ariel Balter(Oregon Health & Science University), Rie Kawashima(Oregon Health & Science University), Gina Choe(Oregon Health & Science University), David Sauer(Oregon Health & Science University), Edward El Rassi(Oregon Health & Science University), Daniel Clayburgh(Oregon Health & Science University), Molly Kulesz‐Martin(Oregon Health & Science University), Eric R. Lutz(Johns Hopkins University), Lei Zheng(Johns Hopkins University), Elizabeth M. Jaffee(Johns Hopkins University), Patrick Leyshock(Oregon Health & Science University), Adam A. Margolin(Oregon Health & Science University), Motomi Mori(Oregon Health & Science University), Joe W. Gray(Oregon Health & Science University), Paul W. Flint(Oregon Health & Science University), Lisa M. Coussens(Oregon Health & Science University)
Cell Reports
April 1, 2017
Cited by 601Open Access
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Abstract

Here, we describe a multiplexed immunohistochemical platform with computational image processing workflows, including image cytometry, enabling simultaneous evaluation of 12 biomarkers in one formalin-fixed paraffin-embedded tissue section. To validate this platform, we used tissue microarrays containing 38 archival head and neck squamous cell carcinomas and revealed differential immune profiles based on lymphoid and myeloid cell densities, correlating with human papilloma virus status and prognosis. Based on these results, we investigated 24 pancreatic ductal adenocarcinomas from patients who received neoadjuvant GVAX vaccination and revealed that response to therapy correlated with degree of mono-myelocytic cell density and percentages of CD8+ T cells expressing T cell exhaustion markers. These data highlight the utility of in situ immune monitoring for patient stratification and provide digital image processing pipelines to the community for examining immune complexity in precious tissue sections, where phenotype and tissue architecture are preserved to improve biomarker discovery and assessment.


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