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A laboratory technician performs hemaggluttination inhibition (HI) testing. China. 2014-2015 flu season.
Scientists use the HI assay to antigenically characterize circulating seasonal influenza viruses.
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A laboratory technician performs hemaggluttination inhibition (HI) testing. China. 2014-2015 flu season.
Scientists use the HI assay to antigenically characterizecirculating seasonal influenza viruses.
Data reported in CDC China’s latest surveillance report(Week 11) indicate that mainland China is experiencing their flu season. Influenza A(H1N1)pdm09, influenza A (H3N2), and influenza B viruses are co-circulating and influenza B viruses are predominating.
China CDC is responsible for influenza surveillance in 1.3 billion people. Thanks in part to a mutually beneficial collaboration with CDC’s Influenza Division over the past two decades, China’s National Influenza Center (CNIC) in Beijing was designated by the WHO as the fifth WHO Collaborating Center for Reference and Research on Influenza in humans in October 2010. With this distinction, China joined Australia, Japan, United Kingdom, and the U. S. CDC in playing a pivotal role in global influenza surveillance.
“Antigens” are molecular structures on the surface of viruses that are recognized by the immune system and are capable of triggering an immune response (antibody production). On influenza viruses, the major antigens are found on the virus’ surface proteins (see Figure 1).
Antigenic Characterization
When someone is exposed to an influenza virus (either through infection or vaccination) their immune system makes specific antibodies against the antigens (surface proteins) on that particular influenza virus. The term “antigenic properties” is used to describe the antibody or immune response triggered by the antigens on a particular virus. “Antigenic characterization” refers to the analysis of virus’ antigenic properties to help assess how related it is to another virus.
CDC antigenically characterizes about 2,000 influenza viruses every year to compare how similar currently circulating influenza viruses are to those that were included in the influenza vaccine, and to monitor for changes in circulating influenza viruses. Antigenic characterization can give an indication of the flu vaccine’s ability to produce an immune response against the influenza viruses circulating in people. This information also helps experts decide what viruses should be included in the upcoming season's influenza vaccine.
Other information that determines how similar a circulating virus is to a vaccine virus or another virus are the results of serology tests and genetic sequencing.
The Hemagglutinin Inhibition Assay (HI Test)
Scientists use a test called the hemagglutinin inhibition (HI) assay to antigenically characterize influenza viruses. The HI test works by measuring how well antibodies bind to (and thus inactivate) influenza viruses.
Scientists use the HI test to assess the antigenic similarity between influenza viruses. This test is particularly useful for helping to select the vaccine viruses used in the seasonal flu vaccine. HI test results can tell us whether antibodies developed against vaccination with one virus are antigenically similar enough to another circulating influenza virus to produce an immune response against that circulating virus. Scientists also use the HI test to compare antigenic changes in currently circulating influenza viruses with influenza viruses that have circulated in the past.
The HI test involves three main components: antibodies, influenza virus, and red blood cells that are mixed together in the wells (i.e., cups) of a microtiter plate. (See Image 1.)
The antibodies used in the HI test are obtained by infecting an animal (usually a ferret) that has not been exposed to any influenza virus or vaccine. The animal’s immune system creates antibodies in response to the antigens on the surface of the specific flu virus that was used to infect that animal. To study these antibodies, a sample of blood (serum) is drawn from the animal. The HI test measures how well these antibodies recognize and bind to other influenza viruses (for example, influenza viruses that have been isolated from flu patients). If the ferret antibodies (that resulted from exposure to the vaccine virus) recognize and bind to the influenza virus from a sick patient, this indicates that the vaccine virus is antigenically similar to the influenza virus obtained from the sick patient. This finding has implications for how well the vaccine might work in people. See Flu Vaccine Effectiveness: Questions and Answers for Health Professionals for more information.
As previously mentioned, the influenza viruses used in the HI test are taken from samples from sick people. CDC and other WHO collaborating centerscollect specimens from people all over the world to track which influenza viruses are infecting humans and how they are evolving.
For the HI test, red blood cells (RBC) are taken from animals (usually turkeys or guinea pig). They are used in the HI test because influenza viruses bind to them. Normally, RBCs in a solution will sink to the bottom of the assay well and form a red dot at the bottom (Figure 2A). However, when an influenza virus is added to the RBC solution, the virus’ hemagglutinin (HA) surface proteins will bind to multiple RBCs. When influenza viruses bind to the RBCs, the red cells form a lattice structure (Figure 2B). This keeps the RBCs suspended in solution instead of sinking to the bottom and forming the red dot. The process of the influenza virus binding to RBCs to form the lattice structure is called “hemagglutination.”
When antibodies are pre-mixed with influenza virus followed by RBCs, the antibodies will bind to influenza virus antigens that they recognize, covering the virus so that its HA surface proteins can no longer bind to RBCs (Figure 2C). The reaction between the antibody and the virus inhibits (i.e., prevents) hemagglutination from occurring, which results in hemagglutination inhibition (as shown in Figure 2C). This is why the assay is called a “hemagglutinin inhibition (HI) test.” Hemagglutination (as depicted in Figure 2B) occurs when antibodies do not recognize and bind to the influenza viruses in the solution, and as a result, the influenza viruses bind to the red blood cells in the solution, forming the lattice structure. When the antibodies do recognize and bind to the influenza viruses in the solution, this shows that the vaccine virus (like the one the ferrets were infected with) has produced an immune response against the influenza virus obtained from the sick patient. When this happens, the influenza virus being tested is said to be “antigenically like” the influenza virus that created the antibodies (from ferrets).
Antibodies do not recognize and bind to antigens from influenza viruses that are antigenically different. If the antibodies do not bind to the antigens on the surface of the influenza virus from the sick patient using the HI assay, hemagglutination occurs. This indicates that the vaccine virus has not caused an immune response against the influenza virus obtained from the sick patient.
Assessing Antigenic Similarity Using the HI Test
The HI test assesses the degree of antigenic similarity between two viruses using a scale based on greater dilutions of antibodies. As previously mentioned, the HI test is performed using a microtiter plate. The microtiter plate contains rows and columns of wells (i.e., cups) where RBCs, influenza virus and antibodies (developed against a comparison virus, such as a vaccine virus) are mixed. Dilutions are marked across the top of the microtiter plate. These dilutions function as a scale for assessing antigenic similarity and immune response. By testing the ability of greater dilutions of antibody to prevent hemagglutination, scientists measure how well those antibodies recognize and bind to (and therefor inactivate) an influenza virus. The higher the dilution, the fewer antibodies are needed to block hemagglutination, the more antigenically similar the two viruses being compared are to each other. The highest dilution of antibody that results in hemagglutinin inhibition is considered a virus’s HI titer (Figure 3). Higher HI titers are associated with greater antigenic similarity. Greater antigenic similarity suggests that vaccination would produce an immune response against the test virus.
Public health experts consider influenza viruses to be antigenically similar or “like” each other if their HI titers differ by two dilutions or less. (This is equivalent to a two-well (i.e., a four-fold dilution) or less difference). Using figure 4 as an example, when circulating virus 1 is compared to a vaccine virus, circulating virus 1 differs by one dilution (a 2-fold difference) and therefore is “like” the previous season’s vaccine virus. However, circulating virus 2 differs by five dilutions (a 32-fold difference) and therefore is not like the previous season’s vaccine virus. Circulating viruses that are antigenically dissimilar (i.e., not “like”) the reference panel are considered “low reactors.”
Limitations
Antigenic characterization gives important information about whether vaccine made using the vaccine virus will protect against circulating influenza viruses, but there are several limitations to antigenic characterization test methodology, which are described below.
Egg Adaptations
Right now, the viruses used to make influenza vaccines must be grown in eggs. This is a current requirement for flu vaccine produced in the United States. As human influenza viruses adapt to grow in eggs, genetic changes can occur in the viruses. These are called “egg-adapted” changes. Some egg-adapted changes may have antigenic (or immunogenic) implications while others may not. Cell-based vaccine production could help eliminate egg-adapted changes.
Time from Vaccine Virus Selection to Delivery of Vaccine
Using current vaccine production technology, it takes about 6-8 months from the time that the vaccine virus is chosen to the time when influenza vaccines become widely available. Because influenza viruses are constantly changing, circulating influenza viruses may change during the time between when vaccine viruses are chosen (i.e., February for the Northern Hemisphere flu vaccine) and when the next season begins. If these changes are antigenically significant, it could mean that antibodies created through vaccination may not recognize and inactivate circulating viruses. New technologies to shorten the manufacturing time for production of influenza vaccine could reduce the chances of significant antigenic changes occurring before people can be vaccinated.
Use of Animals
Use of the HI test to assess the similarity of circulating influenza viruses to vaccine viruses involves obtaining antibodies from animals (particularly ferrets). The ferrets used for making antibodies for the HI test are “immunologically naïve,” which means that they have never been exposed to an influenza virus before and have no antibodies against influenza until after they are infected. When ferrets are infected with a live influenza virus they typically produce strong antibody responses against the influenza virus used to infect the ferret but little to no antibody against other influenza strains. As a result, HI tests (when conducted using immunologically naïve ferrets) are the most sensitive method available for detecting antigenic differences between influenza viruses.
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