Immunohistochemistry for Tumor-Infiltrating Immune Cells After Oncolytic Virotherapy

• Published in: Methods in molecular biology (Clifton, N.J.) Vol. 2058; p. 179
• Main Authors: Saha, Dipongkor, Rabkin, Samuel D
• Format: Journal Article
• Language: English
• Published: United States 01.01.2020
• Subjects: Animals; Antigens, Neoplasm - immunology; Genetic Therapy; Genetic Vectors - genetics; Humans; Immunohistochemistry - methods; Lymphocytes, Tumor-Infiltrating - immunology; Lymphocytes, Tumor-Infiltrating - pathology; Mice; Neoplasms - immunology; Neoplasms - metabolism; Neoplasms - pathology; Neoplasms - therapy; Oncolytic Virotherapy - methods; Oncolytic Viruses - genetics; Tumor Microenvironment - immunology; Tumor-Associated Macrophages - immunology; Tumor-Associated Macrophages - metabolism; Tumor-Associated Macrophages - pathology; Immunohistochemistry; Substrate-based immunohistochemistry; Antigen retrieval; Antigen–antibody reaction; Dual-color immunohistochemistry; Virotherapy; Oncolytic herpes simplex virus; Immune cells
• ISSN: 1940-6029
• DOI: 10.1007/978-1-4939-9794-7_11

Immunohistochemistry (IHC) is an integral laboratory staining technique, which is used for the detection of immune cells in mouse/human tissues or tumors. Oncolytic herpes simplex virus (oHSV) treatment or virotherapy of solid tumors results in antitumor immune responses and infiltration of a variety of immune cells into the tumor. Here, we describe a step-by-step chromogen/substrate-based single- and dual-color IHC protocol to stain immune cells in formalin-fixed, paraffin-embedded mouse glioblastoma (GBM) brain tumor sections after oHSV virotherapy. Tumor sections are deparaffinized with xylene, then gradually rehydrated using ethanol, followed by heat-mediated antigen retrieval using appropriate buffers. Tumor sections are incubated with primary antibodies, which detect a specific immune cell antigen, then incubated with peroxidase- or phosphatase-labeled secondary antibodies, followed by incubation with a color-producing substrate and color visualization (of immune cells) by light microscopy. The protocol described herein is also applicable to detect immune cells in other mouse and human tumors or organs after other forms of immunotherapy.