The yellow fever vaccine provides protection against the yellow fever virus, prevalent in Africa and South America. Immunity typically develops within ten days of vaccination, with 99% protection achieved within a month, offering what appears to be lifelong immunity. The vaccine is effective for controlling disease outbreaks. It is administered via injection, either intramuscularly or subcutaneously.
In 1912, the opening of the Panama Canal increased global exposure to yellow fever. This event led to the first modern attempts to develop a yellow fever vaccine.
In 1937, Max Theiler, Hugh Smith, and Eugen Haagen at the Rockefeller Foundation discovered the 17D strain, a highly effective attenuated virus. Theiler also used chicken eggs to culture the virus, following the work of Ernest Goodpasture.
In 1938, the yellow fever vaccine came into use. It is composed of a weakened yellow fever virus and is included on the World Health Organization's List of Essential Medicines. Certain countries mandate a yellow fever vaccination certificate for travelers arriving from countries where the disease is prevalent.
By 1939, after field trials in Brazil, over one million people had been vaccinated with the 17D strain without severe complications.
In 1941, researchers at Rocky Mountain Laboratories developed a safer "aqueous-base" version of the 17D vaccine using distilled water combined with the virus grown in chicken eggs.
Between 1941 and 1942, Theiler's vaccine was responsible for the largest outbreak of hepatitis B in history, infecting 330,000 soldiers and giving 50,000 jaundice.
In 1951, Max Theiler received the Nobel Prize in Physiology or Medicine for his work on the yellow fever vaccine.
The French neurotropic vaccine (FNV) was not recommended after 1961 due to a higher incidence of encephalitis.
Between 1970 and 2002, only nine cases of yellow fever were reported in unvaccinated travelers from the United States and Europe who traveled to West Africa and South America, and 8 of the 9 died.
Since 1971, screening technology for HBV has been available and is routinely used in situations where HBV contamination is possible including vaccine preparation.
In 1988, there was only one documented nonfatal case of yellow fever in a vaccinated traveler from Spain who visited several West African countries.
In 1996–2001, seven people developed system failure within two to five days of the yellow fever vaccine. The CMAJ article cites that "3 demonstrated histopatholic changes consistent with wild yellow fever virus."
In 2001, the Canadian Medical Association Journal (CMAJ) published an article entitled "Yellow fever vaccination: be sure the patient needs it". The article highlighted instances of system failure and deaths following vaccination, even in travelers to regions without reported yellow fever.
Between 1970 and 2002, only nine cases of yellow fever were reported in unvaccinated travelers from the United States and Europe who traveled to West Africa and South America, and 8 of the 9 died.
In 2010, the online edition of the Center for Disease Control Traveler's Health Yellow Book stated that between 1970 and 2002 only "nine cases of yellow fever were reported in unvaccinated travelers from the United States and Europe who traveled" to West Africa and South America, and 8 of the 9 died.
Since 2011, Gavi-supported vaccination campaigns have covered 88 million people in 14 countries considered at "high-risk" of a yellow fever outbreak.
On 17 May 2013, the World Health Organization (WHO) Strategic Advisory Group of Experts on immunization (SAGE) announced that a booster dose of yellow fever (YF) vaccine, ten years after a primary dose, is not necessary.
UNICEF reported in 2013 that supplies of the yellow fever vaccine were insufficient, with manufacturers producing about 35 million of the 64 million doses needed per year.
Demand for yellow fever vaccine for preventive campaigns has increased from about five million doses per year to a projected 62 million per year by 2014.
In March 2016, emergency stockpiles of yellow fever vaccine diverted to Angola, which consisted of about 10 million doses, had become exhausted.
By May 2016, the emergency stockpiles of yellow fever vaccine diverted to Angola were being replenished.
On 17 June 2016, the WHO agreed to the use of one-fifth the usual dose of yellow fever vaccine as an emergency measure during the ongoing outbreak in Angola and the DR Congo.
As of 2018, newer yellow fever vaccines, based on vero cells, are in development.
As of January 2019, the yellow fever 17D vaccine is considered safe, with over 500 million doses given and very few documented cases of vaccine-associated illness (62 confirmed cases and 35 deaths).
As of February 2021, UNICEF reported awarded contract prices for the yellow fever vaccine ranging from US$0.97 to US$1.444 per dose under multi-year contracts with various suppliers.
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