Published on in Vaccine News
Since 2003, when the nasal spray flu vaccine, known as FluMist®, was introduced, many — especially those wanting to avoid an injection — preferred it. However, in June 2016, the Centers for Disease Control and Prevention (CDC) stopped recommending this version due to ineffectiveness.
In this video, Understanding What Happened with the Intranasal Flu Vaccine, Dr. Offit addresses why FluMist® was taken off the market in 2016 and the changes that were made to make it more effective, so that it could be used again beginning 2018.
Understanding What Happened with the Intranasal Flu Vaccine
Paul A. Offit, MD: Hi, my name is Paul Offit. I’m talking to you today from the Vaccine Education Center here at the Children’s Hospital of Philadelphia. One question that I recently have been asked here at the center is: what’s the story with the flu vaccine? How come now there is this nasal spray flu vaccine that’s available that wasn’t available for a few years? What happened? Why did it go off the market? And why is it back on the market now?
So I think the easiest way to understand this is to start at the beginning. The first flu vaccine was actually developed in the late 1940s. And it was made by taking influenza virus, growing it in eggs, purifying it, and then inactivating it with a chemical so that it couldn’t reproduce itself. And that vaccine was given as a shot. We basically have been using that vaccine – that strategy to make a vaccine – since the late 1940s. And it’s effective at preventing pneumonia that’s caused by influenza.
Now, in 2003, there was a different strategy used to make the flu vaccine. Now, instead of taking influenza virus and inactivating it, this is a live, weakened form of the virus that’s not given as a shot. It was given as a spray in the nose, where the virus would then reproduce itself and induce an immune response without causing disease. Now that vaccine came onto the market in the United States in 2003.
In 2014, it was actually given a preferential recommendation by the Center for Disease Control and Prevention, or CDC, which is to say that the CDC actually preferred the nasal spray for the vaccine to the inactivated vaccine given as a shot.
However, for three years in a row, that vaccine underperformed the inactivated vaccine, (the vaccine given as a shot). And for that reason, although the vaccine was still licensed and still arguably could have been purchased, because the CDC said that they did not any longer recommend that vaccine, it basically was taken off the market.
So now it’s back. And so what happened? I think the problem with that vaccine was that one of the strains, the so-called H1N1 strain, which was actually the strain that caused the influenza pandemic in 2009, didn’t reproduce itself efficiently. So when you give, in this case, four different strains and inoculate it onto the lining of the nose, you have to make sure that all four strains reproduce themselves in the same manner, the same efficiency. Otherwise, one of those strains, in this case the H1N1 strain, didn’t reproduce itself well. And so the immune response was consistently poor, especially when you had a predominant so-called H1N1 year.
Now the company has, I think, gone a long way to solving that problem. They’ve now proven that when they give this vaccine to human nasal epithelial cells, the cells that line our nose, that all four viruses replicate equally. They’ve replaced the H1N1 strain that wasn’t replicating as well with a strain that now clearly does replicate well. They’ve shown that the immune response is now as good as it had been in the past. So now for all practical purposes, this vaccine has come back on the market and I suspect will be as effective as it was before it was taken off the market and now that, I think, that they’ve solved the problem. So that’s what happened to FluMist. Thank you.
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Materials in this section are updated as new information and vaccines become available. The Vaccine Education Center staff regularly reviews materials for accuracy.
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