The development suggests that the United States may be able to vaccinate hundreds of thousands more people than anticipated by the end of the year.
-
Send any friend a story
As a subscriber, you have “>10 gift articles to give each month. Anyone can read what you share.
Give this article
- Read in app
People wait in line for the monkeypox vaccine in New York. Supplies of the vaccine have been short as the outbreak spreads in the U.S.
WASHINGTON — After two months of a vaccine shortage that has undermined its response to the monkeypox outbreak, the Biden administration on Tuesday moved to stretch its limited supplies by authorizing a different injection method that will use one-fifth of the current dose.
At the same time, some promising news emerged from Denmark, where the world’s only producer of the main monkeypox vaccine, Jynneos, indicated that a large number of doses previously thought to have expired might actually still be usable.
The developments suggest that the United States may be able to vaccinate hundreds of thousands more people at risk for monkeypox than anticipated by the end of the year. That could significantly help curb an outbreak that has infected nearly 9,000 Americans since May, and that some experts fear could spill over from high-risk groups to the broader population.
Injecting the vaccine between layers of the skin, instead of into the underlying fat, will be “a game changer when it comes to our response and our ability to get ahead of the virus,” said Robert J. Fenton Jr., the new White House monkeypox response coordinator, at a news briefing. “It’s safe, it’s effective, and it will significantly scale the volume of vaccine doses available.”
Federal officials estimate that the government can vaccinate up to five times as many people using so-called intradermal injections instead of the standard subcutaneous ones. The government issued a public health emergency declaration, the second in less than a week, enabling the Food and Drug Administration to authorize the new regimen.
The F.D.A. also used its emergency powers to authorize the vaccine for people under 18 who are at high risk of infection, citing an uptick in potential exposures in that age group. Previously, doctors had to ask the agency’s permission to vaccinate each child. At least five children have been diagnosed with monkeypox, and dozens more underwent screening after an Illinois day care worker was found to be infected last week.
The United States once had more than 20 million doses of Jynneos in the national stockpile. It still owns 16.5 million doses of bulk vaccine, stored in freezers at the headquarters of the manufacturer, Bavarian Nordic, outside Copenhagen. But the stockpile doses gradually expired over the past decade. After the outbreak began in mid-May, the government was slow to request that the bulk vaccine be processed into vials, ending up in a queue behind other countries that are also fighting monkeypox.
Now the Biden administration is scrambling to find a substitute firm that can bottle and label the bulk vaccine faster than Bavarian Nordic. It is also working with Bavarian Nordic to test whether some of the expired doses in the stockpile remain potent, even though the newest are already eight years old and at the end of their expected shelf life, according to firm’s chief executive, Paul Chaplin.
Since monkeypox turned up here in May, the federal government has shipped local jurisdictions only 670,000 doses, although officials say they have roughly another half-million doses of the two-shot vaccine in hand. Those shots are enough to cover only about one-third of the 1.6 million to 1.7 million individuals the Centers for Disease Control and Prevention have identified as high risk. For now, the virus is primarily spreading primarily among men who have sex with men.
Changing the injection method appears to be the quickest fix for the shortage, although some experts said they worry that the data showing that will work is essentially limited to one study published in 2015 and sponsored by the National Institutes of Health. Researchers compared the intradermal approach with the standard injection method and found the intradermal shots triggered a comparable level of neutralizing antibodies using one-fifth as much of the monkeypox vaccine. They also caused more redness, swelling and itching at the injection site.
What to Know About the Monkeypox Virus
Card 1 of 7
What to Know About the Monkeypox Virus
What is monkeypox? Monkeypox is a virus similar to smallpox, but symptoms are less severe. It was discovered in 1958, after outbreaks occurred in monkeys kept for research. The virus was primarily found in parts of Central and West Africa, but recently it has spread to dozens of countries and infected tens of thousands of people, overwhelmingly men who have sex with men.
What to Know About the Monkeypox Virus
What are the symptoms? People who get sick commonly experience a fever, headache, back and muscle aches, swollen lymph nodes, and exhaustion. A few days after getting a fever, most people also develop a rash that starts with flat red marks that become raised and filled with pus. On average, symptoms appear within six to 13 days of exposure, but can take up to three weeks.
What to Know About the Monkeypox Virus
How does it spread? The monkeypox virus can spread from person to person through close physical contact with infectious lesions or pustules, by touching items — like clothing or bedding — that previously touched the rash, or via the respiratory droplets produced by coughing or sneezing. Monkeypox can also be transmitted from mother to fetus via the placenta or through close contact during and after birth.
What to Know About the Monkeypox Virus
I fear I might have monkeypox. What should I do? There is no way to test for monkeypox if you have only flulike symptoms. But if you start to notice red lesions, you should contact an urgent care center or your primary care physician, who can order a monkeypox test. Isolate at home as soon as you develop symptoms, and wear high-quality masks if you must come in contact with others for medical care.
What to Know About the Monkeypox Virus
What is the treatment for monkeypox? If you get sick, the treatment for monkeypox generally involves symptom management. Tecovirimat, a hard-to-obtain antiviral drug also known as TPOXX, occasionally can be used for severe cases. The Jynneos vaccine, which protects against smallpox and monkeypox, can also help reduce symptoms, even if taken after exposure.
What to Know About the Monkeypox Virus
Who can get the vaccine? Jynneos vaccine is most commonly used to prevent monkeypox infections, and consists of two doses given four weeks apart. It has mostly been offered to health care workers and people who have had a confirmed or suspected exposure due to limited supplies, though new doses should become available in the coming months. A few states, including New York, have also made vaccines available among higher-risk populations.
What to Know About the Monkeypox Virus
I live in New York. Can I get the vaccine? Adult men who have sex with men and who have had multiple sexual partners in the past 14 days are eligible for a vaccine in New York City, as well as close contacts of infected people. Eligible people who have conditions that weaken the immune system or who have a history of dermatitis or eczema are also strongly encouraged to get vaccinated. People can book an appointment through this website.
At the briefing, Dr. Robert M. Califf, director of the F.D.A., called those side effects manageable. And Dr. Peter Marks, who oversees the agency’s vaccine regulation, said the monkeypox vaccine was “given to thousands of people intradermally” in Germany and the method is “not at all new.”
Federal officials are anxious for states and localities to adopt the new type of injection as quickly as possible, even though vaccinators are more familiar with the standard approach. Dr. Rochelle P. Walensky, director of the Centers for Disease Control and Prevention, said the agency is offering training seminars and other information to help bring vaccinators up to speed.
The federal government is also hoping that with more ample supply, jurisdictions will no longer give people only the first of two doses in order to conserve supply. “There is data saying that is not protective enough,” Dr. Walensky warned. Research has shown that a single shot triggers a far weaker immune response that two.
Dr. Walensky also said that vaccinated individuals should continue “avoiding close skin-to-skin contact, including intimate contact, with somebody who has monkeypox because we don’t yet know how well these vaccines work.”
The Jynneos vaccine was licensed by the F.D.A. in 2019 for use against both monkeypox and smallpox without a large-scale clinical trial that studied effectiveness. Dr. Califf said none was conducted because there were never enough cases in the United States. Studies showed that, compared with an earlier, approved vaccine, Jynneos provoked a stronger immune response.
The intradermal method should diminish U.S. demand for new doses, which would presumably mean less profit for Bavarian Nordic. In a Tuesday morning interview, Mr. Chaplin, the company’s chief executive officer, said he hoped that the government would monitor at least some of those who are vaccinated in that way to gather more safety data.
Since last Thursday, when federal officials first said they were considering the intradermal method, he said, the company has been “bombarded” with calls from state officials asking how it would work, including how many times a vial could be punctured and how long the vaccine would remain potent once the seal on the vial had been broken.
“We’re now scrambling to try and get a hold of the C.D.C. and see what the official position will be because frankly, we don’t know,” he said. “We don’t know how long you can keep the vial once you puncture it.”
Mr. Chaplin also said that the company is busily testing samples of older doses that had sat for years in the government’s national stockpile, past their three-year expiration date. He described the results as promising. Up to a million doses that were manufactured in 2014 might still be usable, he suggested, but not for long.
“There is not a lot of time to hang around before we use them,” he said. “We’ve still got months, I would say.”
ImageA laboratory of Bavarian Nordic in Martinsried, Germany. The company’s smallpox vaccine is also effective against monkeypox.Credit…Lukas Barth/Reuters
Some activists expressed concern that the White House was embracing what they viewed as relatively risky solutions to the shortage when it could use the government’s authority under the Defense Production Act to force an American company to bottle and label the bulk vaccine that is in storage at Bavarian Nordic’s headquarters.
“There are 15 million doses that they haven’t figured out how to get into vials, and instead they’re doing this really aggressive dose-sparing strategy,” said James Krellenstein, a Brooklyn-based gay health activist who has been urging federal health officials to expand access to the vaccine. He noted that the federal government had used the Defense Production Act to speed up aspects of Covid-19 vaccine production.
But vaccine production experts said that it would take an American company at least three months to gear up to handle the final manufacturing phase, known as fill and finish, regardless of how much pressure the White House exerted. Federal officials have been canvassing pharmaceutical companies for weeks, looking for one that will take on the work.
Source: nytimes.com
