TY - JOUR
T1 - Immunohistochemistry for Tumor-Infiltrating Immune Cells After Oncolytic Virotherapy
AU - Saha, Dipongkor
AU - Rabkin, Samuel D.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - 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.
AB - 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.
KW - Antigen retrieval
KW - Antigen–antibody reaction
KW - Dual-color immunohistochemistry
KW - Immune cells
KW - Immunohistochemistry
KW - Oncolytic herpes simplex virus
KW - Substrate-based immunohistochemistry
KW - Virotherapy
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UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85071772896&origin=inward
U2 - 10.1007/978-1-4939-9794-7_11
DO - 10.1007/978-1-4939-9794-7_11
M3 - Article
C2 - 31486038
SN - 1064-3745
VL - 2058
SP - 179
EP - 190
JO - Methods in Molecular Biology
JF - Methods in Molecular Biology
ER -