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| − | |sublink1 =Immunological testing - WikiBlood
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| − | |subtext1 =IMMUNOLOGICAL TESTING
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| | ==Introduction== | | ==Introduction== |
| | The radioimmunoassay (RIA) is a sensitive technique used to detect the presence of antigen in a sample using radiolabelled antibodies. Developed in the 1960's, the RIA proved a powerful tool in antigen detection, although the procedure was soon overtaken by ELISA, which utilises enzymes rather than radioactive labels. RIAs are still used today however, to measure: | | The radioimmunoassay (RIA) is a sensitive technique used to detect the presence of antigen in a sample using radiolabelled antibodies. Developed in the 1960's, the RIA proved a powerful tool in antigen detection, although the procedure was soon overtaken by ELISA, which utilises enzymes rather than radioactive labels. RIAs are still used today however, to measure: |
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| | ==Technique== | | ==Technique== |
| − | *The antigen is often labelled with a gamma-emitting isotope, e.g. iodine-125 | + | *The antigen is often labeled with a gamma-emitting isotope, e.g. iodine-125 |
| − | **Beta-emtting isotopes such as tritium are also often used | + | **Beta-emitting isotopes such as tritium are also often used |
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| − | # Determine the amount of antibody required to bind ~50% of radiolabelled antigen in mixture- ''required to ensure the number of epitopes presented by labelled antigen exceeds number of antibody binding sites'' | + | # Determine the amount of antibody required to bind ~50% of radiolabeled antigen in mixture- ''required to ensure the number of epitopes presented by labeled antigen exceeds number of antibody binding sites'' |
| − | # Add unlabelled antigen to mixture | + | # Add unlabeled antigen to mixture |
| | # Separate antigen-antibody complex from free antigen by precipitation | | # Separate antigen-antibody complex from free antigen by precipitation |
| | # Measure radioactivity in precipitate | | # Measure radioactivity in precipitate |
| | *There are various methods to separate the antigen-antibody complexes from the free antigen: | | *There are various methods to separate the antigen-antibody complexes from the free antigen: |
| − | **Precipitate complexes using secondary isotype-specific antiimmunoglobulin | + | **Precipitate complexes using secondary isotype-specific anti-immunoglobulin |
| − | **If complex contains IgG, it can be removed by mixing with formalin-killed ''Staphylococcus aureus''- protein A of ''S. aureus'' has a high affinity for IgG | + | **If complex contains [[IgG]], it can be removed by mixing with formalin-killed ''Staphylococcus aureus''- protein A of ''S. aureus'' has a high affinity for [[IgG]] |
| − | *** Removal of the complex by either of these methods leaves an amount of free labelled antigen in the supernatant (liquid section from precipitation)- the radioactivity of this can be measured and the value taken away from the total amount of labelled antigen added (known amount)= amount of bound labelled antigen | + | *** Removal of the complex by either of these methods leaves an amount of free labeled antigen in the supernatant (liquid section from precipitation)- the radioactivity of this can be measured and the value taken away from the total amount of labeled antigen added (known amount)= amount of bound labeled antigen |
| | **A number of solid-phase RIAs have been developed | | **A number of solid-phase RIAs have been developed |
| − | ***Sometimes the antibody can be absorbed onto the surface- the amount of radiolabelled antigen bound to the beads can be measured after washing | + | ***Sometimes the antibody can be absorbed onto the surface- the amount of radiolabeled antigen bound to the beads can be measured after washing |
| | ***Antibody can be immobilised on PVC or polystyrene | | ***Antibody can be immobilised on PVC or polystyrene |
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| | **RIA used in this way has been employed in the detection of the hepatitis B surface antigen in donor blood, reducing the occurrence of hepatitis infections as a result of blood transfusions in humans | | **RIA used in this way has been employed in the detection of the hepatitis B surface antigen in donor blood, reducing the occurrence of hepatitis infections as a result of blood transfusions in humans |
| | *Measuring plasma levels of hormones and controlled substances | | *Measuring plasma levels of hormones and controlled substances |
| − | *Measuring anti-DNA antibodies present in systemic lupus erythematosus (SLE) | + | *Measuring anti-DNA antibodies present in [[SLE|systemic lupus erythematosus (SLE)]] |
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| − | =Drawbacks= | + | ==Drawbacks== |
| | Although the RIA is a very sensitive test, and therefore widely-used, there are disadvantages to its use: | | Although the RIA is a very sensitive test, and therefore widely-used, there are disadvantages to its use: |
| | *The substances being used are radioactive | | *The substances being used are radioactive |
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| | *Iodine is naturally concentrated in the thyroid gland, whether radioactive or not, and incorporated into thyroxine | | *Iodine is naturally concentrated in the thyroid gland, whether radioactive or not, and incorporated into thyroxine |
| | Consequently, ELISA has largely overtaken RIA as a preferred diagnostic tool | | Consequently, ELISA has largely overtaken RIA as a preferred diagnostic tool |
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| | + | {{review}} |
| | + | <br><br> |
| | + | {{Jim Bee 2007}} |
| | + | [[Category:Immunological Testing]] |