Intro to Immunohistochemistry (IHC) Staining: Steps & Best Practices (2024)

IHC is used in histology to detect the presence of specific protein markers that can assist with accurate tumor classification and diagnosis. IHC has evolved to complement theand Special Stain techniques that typically show tissue morphology (structure). Where H&E and Special Stains are non-specific, IHC is directed to a specific protein marker or markers. IHC is used as a diagnostic tool to assist in the diagnosis of solid tumors and cytological specimens and has been used as a mainstream diagnostic tool for almost half a century.

Target Antigen

Antigens are proteins that are within or on the surface of a cell. Pathologists look for the presence or absence of particular antigens to assist with diagnosis.

There are many hundreds of antigens that have been found to be diagnostically useful. Often, a pathologist will use a “panel” of multiple antigens to help fully classify a particular tumor.

Primary Antibody

The first stage of IHC is the application of a primary antibody that binds specifically to the target antigen.

There are two main types of antibody, polyclonal and monoclonal. Polyclonal antibodies have an affinity with, and bind to, multiple epitopes (or parts) or the target antigen, and as such are more prone to cross-react to non-target antigens.

Monoclonal antibodies have an affinity to only one epitope and tend to produce cleaner, more specific staining but are less sensitive or intense.

Secondary Antibody

Next, secondary antibodies bind to the primary antibody. This is known as indirect IHC. It is now commonly used as multiple secondaries can bind to a single primary to amplify the staining intensity.

Thedetection systembuilds on the secondary. Modern chromogenic detection utilizes enzymes such as Horseradish Peroxidase (HRP) that are conjugated (joined) to an antibody. Multiple enzymes attached to the antibody are known as polymers, and they again produce more intense staining as there are more molecules for the chromogen to attach.

The Chromogen

Finally, a substrate forms an insoluble colored precipitate that can be visualized under a microscope. There are two commonly used chromogens: DAB (brown) or AP (red).

DAB is used for most applications as it provides strong and permanent stains. AP Red (or another red chromogen) is used mainly for skin sections where the brown DAB may be masked by brown melanin pigment.

Both DAB and AP Red are sometimes used in the same tissue section to allow the pathologist to visualize two antigens in the one slide. This is a process known as double staining.

A Completed IHC Stain

This is a typical IHC stain where the brown precipitate indicates the presence of the target antigen – in this case, Cytokeratin 5 on a prostate biopsy. The amount of staining, the staining pattern, and the location of staining (cell cytoplasm nucleus or membrane) all provide information for the diagnosing pathologist.

The blue background is ahematoxylincounter-stain that is often applied after the chromogen. The counter-stain provides a contrast to the chromogen and also helps the pathologist visualize the underlying tissue structure.

From patient to pathologist, preparing tissue specimens for histological examination requires care, skill, and sound procedures. This guide provides practical advice on best-practice techniques and simple ways to avoid common errors.

Tips for better IHC are highlighted in this section. We hope each step provides a valuable reminder of good histology practice and helps with troubleshooting when unacceptable results do occur.

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Step 1 - Use High Quality Sections

Take particular care to use thin, flat sections that have been thoroughly dried onto the slide. Preferably use charged slides or APES coated slides for IHC .

Uneven, poorly-adhering sections stain unevenly with variable background staining.

Step 2 - Ensure Optimal Fixation

Good quality fixation using known and consistent fixation conditions (fixative type, pH, temperature, time) produces the best results. Specimens should be checked prior to processing to determine if further fixation is required.

Inconsistent fixation conditions, producing under-fixed or over-fixed tissues, produce variable results and make troubleshooting difficult.

Step 3 - Avoid Section Adhesion Problems

Avoid the use of protein-based section adhesives in the flotation bath (glue, starch, or gelatin), particularly on charged slides.

Protein-based adhesives can block the surface of the charged slide. This causes inconsistent adhesion and leads to uneven staining due to the pooling of IHC reagents beneath lifting sections.

Step 7 - Optimize Retrieval Methods

Choose appropriate unmasking conditions for the primary antibody being used, the tissue being stained, and the fixation employed (pH, reagent, reaction conditions).

The same retrieval technique is used for all primaries on the assumption that there is a successful universal HIER method.

Step 9 - Block Endogenous Peroxidase

For peroxidase-based detection systems, always use a peroxidase-blocking step.

Non-specific staining is often seen in erythrocytes, granulocytes, monocytes, and in muscle. This is due to incompletely-blocked endogenous peroxidase.

Bonus tip: Choosing the Right Antibodies

A simple, but sometimes overlooked step is to choose antibodies that work for immunohistochemistry. This can save you a lot of headaches down the road. Search for specific antibodies from literature, vendors, as well as your peers.

There are several things to keep in mind with antibodies. What might work well in one laboratory might not be optimal for your laboratory. Each antibody needs to be tested with your staining system. Antibodies over time can lose their staining intensity. Exposure to air and light can cause this.

Concentrates versus RTU antibodies

When selecting antibodies, there are two main options to consider; a concentrated format or a pre-diluted, Ready-To-Use (RTU) format. Concentrates are flexible, have a lower initial purchase price, and can generally be used within any staining system, both automated and manual, subject to the manufacturer’s recommendations. The working dilution of concentrates can be optimized to balance cost, staining time, and quality. Given the large working dilution range, concentrates can be varied at any time to accommodate changes to laboratory practice or for multiple protocols for a particular antibody. However, concentrates do require preparation time and validation. As there is no definitive way of determining the properties and stability of a diluted antibody without well controlled and executed studies, staining quality may be compromised as subtle deteriorations may not be noticed. The advantages of RTUs include increased laboratory efficiency, better quality control, and easier reagent management. They eliminate time spent on working dilution, preparation, and the time to validate the assay. Consistency is enhanced with run-to-run variation reduced, especially in conjunction with automated stainers and associated detection systems. With a defined number of tests and manufacturer-verified expiry, RTUs simplify antibody management. Additionally, RTUs can contribute to laboratory growth by making it easy to adopt new antibody assays as the amount of validation work is greatly reduced.

Bonus tip: Pre-staining standardization is critical

Any pathologist, lab manager, or histotechnologist will readily acknowledge that preparation for
IHC
staining begins the moment tissue is acquired. The literature documents optimal conditions fortissue fixation,processing, andsectioningto ensure morphology and antigenicity are maintained. Further improvements in maintaining consistency to correctly control for these factors could be pursued. This may involve a laboratory establishing itself at the site of collection, recognizing that accessioning and sample preparation begins here.

Automated accession,
LIS
, andsample tracking infrastructureshould extend out of the laboratory and into surgery/point of biopsy, enabling standardized prep-equipment (“controlled” pots, fixatives) to be monitored for optimal processing downstream. A parallel industry that recognized this value is the blood analysis laboratory, which utilizes standardized coated collection vials with barcoded patient information for tracking and accessioning.

Linking fixation, tissue processing, and
IHC
staining will add value to control quality. Laboratories that can monitor and record fixation and tissue processing conditions and link these with
IHC
staining protocols will be able to report a diagnosis under a tighter quality controlled environment. The frequent use of controls for pre-processing variability (e.g., control every 100 slides) may also provide a good measure for staining instrument tolerances and performance. These workflows and technologies will evolve as the
IHC
industry matures. However, there are a number of good practices that are known to establish and maintain high quality and consistent results from
IHC
staining (refer to table below).

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