(immunology) A vaccine prepared from a glycerinated suspension of the exudate from cowpox vesicles obtained from healthy vaccinated calves or sheep. Also known as antismallpox vaccine; glycerinated vaccine virus; Jennerian vaccine; virus vaccinium.
| Sci-Tech Dictionary: smallpox vaccine |
(immunology) A vaccine prepared from a glycerinated suspension of the exudate from cowpox vesicles obtained from healthy vaccinated calves or sheep. Also known as antismallpox vaccine; glycerinated vaccine virus; Jennerian vaccine; virus vaccinium.
| 5min Related Video: Smallpox vaccine |
| Drug Info: Smallpox Vaccine, Vaccinia Vaccine |
Brand names: Dryvax®
Smallpox Vaccine, Vaccinia Vaccine injection
What is Smallpox Vaccine, Vaccinia Vaccine injection?
What should I tell my health care provider before I take this medicine?
They need to know if you or anyone in your household have any of these conditions:
cancer or receiving cancer treatments or radiation therapy
currently sick with a moderate or severe short-term illness or infection
eczema or atopic dermatitis (even if the condition is not currently active, mild, or was experienced as a child)
HIV-infection or AIDS
organ transplant
receiving high-dose corticosteroid therapy
skin conditions such as burns, chickenpox, herpes, impetigo, herpes, psoriasis, severe acne, or shingles
weakened immune system
an unusual reaction to smallpox vaccine, vaccinia vaccine, other medicines, foods, dyes, or preservatives
pregnant or trying to get pregnant within one month of vaccination
breast-feeding
How should this medicine be used?
The smallpox vaccine is only administered by qualified healthcare professionals. It is not given as a shot. The smallpox vaccine is usually given in the upper arm using a two-prong needle that is dipped in the vaccine solution. When the needle is removed from the solution, it retains a droplet of the vaccine. The needle is then used to prick the skin a number of times within a few seconds. The pricking is not deep but will cause a sore spot and one or two droplets of blood to form. The vaccination site is then covered to prevent spreading the virus.
The use of this vaccine must be officially recorded. Federal law requires that the manufacturer's name and lot number; name, address, and phone number of the person giving the vaccine; and the date of administration be recorded in the patient's permanent medical record.
Your health care professional will give you written information on the smallpox vaccine at the time of the vaccination. Be sure to read this information.
If the vaccination is successful, a red and itchy bump develops in 34 days at the vaccination site. Within the first week, the bump becomes a large blister, fills with pus, and begins to drain. In the second week, the blister begins to dry up and a scab forms which falls off in the third week. A small scar remains at the site. A stronger reaction to the vaccine occurs in people who are being vaccinated for the first time.
Contact your pediatrician or health care professional regarding the use of this medicine in children or infants under 12 months of age. Special care may be needed.
What if I miss a dose?
What drug(s) may interact with Smallpox Vaccine, Vaccinia Vaccine?
Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.
What should I watch for while taking Smallpox Vaccine, Vaccinia Vaccine?
After vaccination, there is live virus present at the site. This live virus can be spread to other parts of the body or to other people through contact. To avoid this, the vaccination site should be cared for carefully until the scab that forms falls off on its own (in 2 to 3 weeks). The following instructions should be followed:
WHAT YOU SHOULD DO:
Cover the vaccination site loosely with a gauze bandage, using medical tape to keep it in place. Keep it covered until the scab has separated on its own. This bandage will provide a barrier to protect against spread of the vaccinia virus. (Health care workers involved in direct patient care should cover the gauze with a semi-permeable dressing as an additional barrier.
You can wear a shirt that covers the vaccination site as an extra precaution to prevent spread of the vaccinia virus. This is particularly important in situations of close personal contact.
Change the bandage every 12 days. This will keep skin at the vaccination site from softening and wearing away. Put the contaminated bandages in a sealed plastic bag and throw them away.
Wash hands with soap and warm water after direct contact with the bandage or after direct contact with the vaccination site. This is vital in order to remove any virus from your hands and prevent contact spread.
Keep the vaccination site dry. Cover the vaccination site with a water-resistant pad, such as a waterproof band-aid when you bathe. Remember to change back to the loose gauze bandage after bathing.
Wash clothing or other any material that comes in contact with the vaccination site. Use hot water with detergent and/or bleach.
When the scab comes off, throw it away in a sealed plastic bag (remember to wash your hands afterwards).
WHAT YOU SHOULD NOT DO:
Don't use a bandage that blocks all air from the vaccination site. This may cause the skin at the vaccination site to soften and wear away. Use loose gauze secured with medical tape to cover the site.
Don't put salves or ointments on the vaccination site.
Don't scratch or pick at the scab.
If you are a female who is receiving this vaccine, ask your health care professional about preventing pregnancy. It is recommended that you do not get pregnant in the first month after you receive this vaccine.
What side effects may I notice from receiving Smallpox Vaccine, Vaccinia Vaccine?
Side effects that you should report to your prescriber or health care professional immediately:
difficulty breathing, shortness of breath, wheezing, or difficulty swallowing
infection that spreads from vaccination site (progressive vaccinia)
muscle aches or paralysis
rash or outbreak of sores limited to one area such as genitals or face
swelling of the face or eyes
serious skin rash (eczema vaccinatum); usually in people with history of eczema or other chronic skin condition
seizures
widespread vaccinia rash
Call your health care provider immediately if any of these symptoms occur.
Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome):
armpit glands large and sore
chills
difficulty sleeping
fatigue
general bad feeling
mild fever
vomiting
Where can I keep my medicine?
This does not apply. You will not store smallpox vaccine at home.
Last updated: 7/1/2002
Important Disclaimer: The drug information provided here is for educational purposes only. It is intended to supplement, not substitute for, the diagnosis, treatment and advice of a medical professional. This drug information does not cover all possible uses, precautions, side effects and interactions. It should not be construed to indicate that this or any drug is safe for you. Consult your medical professional for guidance before using any prescription or over the counter drugs.
| Intelligence Encyclopedia: Smallpox Vaccine |
Smallpox, or variola major, is a highly contagious disease that is caused by the variola virus. The name smallpox comes from the Latin word for spotted. A visual hallmark of smallpox is the raised bumps that appear on the victim's face and body. Smallpox is fatal in approximately 25% of cases.
There is no cure for smallpox, and treatment is supportive. Prevention of the disease by the administration of smallpox vaccine is the most effective strategy to eliminate the spread of smallpox. Vaccination, conducted on a worldwide scale, was successful in effectively eliminating smallpox as a naturally occurring disease.
The eradication of smallpox saw the end of routine vaccination programs. As of 2003, no American under the age of 30 routinely receives the vaccine. Even in older Americans, immunity has likely faded. After the bioterrorist anthrax attacks on U.S. citizens in late 2001, concern has heightened that smallpox will be used as a terrorist weapon on a population that is once again susceptible to infection. Beginning in January, 2003, health care workers at strategic hospitals and research centers across the United States received the smallpox vaccine in order to provide a population of immune responders in case of a smallpox out-break or mass exposure due to bioterrorism. Mass vaccination programs are again under study by researchers, and smallpox vaccines are scheduled to be available to all Americans on a voluntary basis by mid-2004.
The only smallpox vaccine that is in use today—a preparation called Dryvax—is made from vaccinia, a poxvirus that is very similar to the smallpox virus. The reaction of the immune system to vaccinia confers protection to the smallpox virus. The vaccinia virus that is administered is alive and causes a mild infection, which is inconsequential in most people. However, in a small minority of people, the use of the live virus does carry a risk that the virus will spread from the site of injection, and that side effects will result.
The side effects are typically minor (e.g., sore arm at the injection site, a fever, and generalized body aches). However, rare severe side effects are possible, which can even be life threatening. These include encephalitis (a swelling of the brain and spinal cord), gangrene, extreme eczema, and blindness. People whose immune systems are not functioning properly are especially at risk, as are those people who have had skin ailments such as eczema or atopic dermatitis. The fatality rate due to the vaccine is estimated to be one in eight million.
Despite the risk, smallpox vaccine is worthwhile if exposure to smallpox is possible. A single injection of vaccinia vaccine preparation provides up to five years of immunity to smallpox. A subsequent injection extends this protection. Studies have demonstrated that up to 95% of vaccinated people are protected from smallpox infection. Protection results after just a few days. If exposure to smallpox is anticipated—such as in a military campaign— vaccination a short time before can be a wise precaution.
Smallpox vaccine is injected using a two-pronged needle dipped into the vaccine solution, which then pricks the skin of an upper arm several times in a few seconds. The injection typically becomes sore, blisters and forms a scab. When the scab falls off, a distinctive scar is left.
Currently, the stockpile of smallpox vaccine in the U.S. is about 15 million doses. The vaccine may be capable of being diluted 10 times without losing its protective potency. This would extend the coverage to 150 million people. As of December 2002, 155 million additional doses of smallpox vaccine are being delivered. The new vaccine is made from cow tissues that were grown in laboratory culture. This technique produces a more uniform vaccine preparation than the old method, where tissue was scraped from the lesions of infected cows.
Other smallpox vaccines. The development of improved smallpox vaccines, and the refinement of existing vaccine preparations, has begun only recently. Research on improved vaccines largely ended when the demand for vaccinations ended in the 1970s.
A form of smallpox vaccine called Modified vaccinia Ankara (MVA) was developed 40 years ago. The vaccinia virus used in this preparation cannot replicate in human cells, but still generates an immune response. While the vaccine appears to produce fewer side effects than the standard vaccinia vaccine, large scale tests have not yet been done.
Another vaccinia strain that has been used to develop a smallpox vaccine is called LC16m8. In contrast to MVA, LC16m8 does replicate inside human cells. However, the virus lacks some of the usual surface proteins that may be important in the immune response.
Genetic engineering is also playing a role in smallpox vaccine development. For example, a vaccinia strain has been engineered that does not form certain proteins unless the antibiotic tetracycline is present. The idea here is that the vaccine and the antibiotic would be taken simultaneously. In the event of an adverse vaccine reaction, use of the antibiotic would be stopped, which would stop the immune reactivity of the vaccinia virus. This approach is still in the laboratory stage.
Further Reading
Books
Institute of Medicine. Assessment of Future Scientific Needs for Live Variola Virus. Washington, DC: National Academy Press, 1999.
Periodicals
Henderson, D.A. "Smallpox: clinical and epidemiologic features." Emerging Infectious Diseases no. 5 (1999): 537–39.
Rosenthal, S.R., M. Merchlinsky, C. Kleppinger, et al. "Developing New Smallpox Vaccines." Emerging Infectious Diseases no. 7 (2001): 920–26.
Electronic
Centers for Disease Control and Prevention. "Smallpox Factsheet: Vaccine Overview." Public Health Emergency Preparedness and Response. December 9, 2002. <http://www.bt.cdc.gov/agent/smallpox/vaccination/facts.asp>(31 December 2002).
| Medical Dictionary: smallpox vaccine |
A vaccine containing vaccinia virus suspensions that is inoculated subcutaneously to immunize against smallpox.
| Wikipedia: Smallpox vaccine |
The smallpox vaccine was the first successful vaccine to be developed. The process of vaccination was discovered by Edward Jenner in 1796, who acted upon his observation that milkmaids who caught the cowpox virus did not catch smallpox.[1] Prior to widespread vaccination, mortality rates in individuals with smallpox were high—up to 35% in some cases.[2]
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Before the introduction of a vaccine, the mortality of the severe form of smallpox—variola major—was very high. Historical records show that a method of inducing immunity was already known. A process called inoculation, also known as insufflation or variolation was practiced in India as early as 1000 BC.[3]. This interpretation is disputed, however: other investigators contend the ancient Sanskrit medical texts of India do not describe these techniques.[4] The first clear reference to smallpox inoculation was made by the Chinese author Wan Quan (1499–1582) in his Douzhen xinfa (痘疹心法) published in 1549.[5] Inoculation for smallpox does not appear to have been widespread in China until the reign era of the Longqing Emperor (r. 1567–1572) during the Ming Dynasty.[6] In China powdered smallpox scabs were blown up the noses of the healthy. The patients would then develop a mild case of the disease and from then on were immune to it. The technique did have a 0.5-2% mortality rate, but that was considerably less than the 20-30% mortality rate of the disease itself.
Variolation was also practiced throughout the latter half of the 17th century by physicians in Turkey, Persia, and Africa. In 1714 and 1716 two reports of the Turkish method of inoculation were made to the Royal Society in England, by Emmanuel Timoni, a doctor affiliated with the British Embassy in Istanbul,[7] and Jacob Pylarini. Lady Mary Wortley Montagu, wife of the British ambassador, is widely credited with introducing the process to Great Britain in 1721. The procedure had been performed on her son and daughter, aged 5 and 4 respectively. They both recovered quickly. In 1721, an epidemic of smallpox hit London and left the British Royal Family in fear.[7] Reading of Lady Wortley Montagu’s efforts, they wanted to use inoculation on themselves. Doctors told them that it was a dangerous procedure, so they decided to try it on other people first. The test subjects they used were condemned prisoners. The doctors inoculated the prisoners and all of them recovered in a couple of weeks. So assured, the British royal family inoculated themselves and reassured the English people that it was safe.
| “ | ...scarred the wrists, legs, and forehead of the patient, placed a fresh and kindly pock in each incision and bound it there for eight or ten days, after this time the patient was credibly informed. The patient would then develop a mild case [of smallpox], recover, and thereafter be immune.[8] | ” |
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—Dr. Peter Kennedy |
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Stimulated by a severe epidemic, variolation was first employed in North America in 1721. The practice had been known in Boston since 1706, when Cotton Mather (of Salem witch trial fame) discovered that his slave, Onesimus had been inoculated while still in Africa and that many slaves imported to Boston had also received inoculations.[9] The practice was, at first, widely criticized.[10] However a limited trial showed that 6 deaths occurred out of 244 who were vaccinated (2.5%) while 844 out of 5980 died of natural disease, and the process was widely adopted throughout the colonies.[11] By 1777 George Washington, who initially hesitated to have his Revolutionary War troops inoculated during a smallpox outbreak writing, “should We inoculate generally, the Enemy, knowing it, will certainly take Advantage of our Situation;”, eventually ordered mandatory inoculation of all troops and recruits who had not had the disease.[12]
This technique was documented as having a mortality rate of only one in a thousand. Two years after Kennedy's description appeared, March 1718, Dr. Charles Maitland successfully inoculated the five-year-old son of the British ambassador to the Turkish court under orders from the ambassador's wife Lady Mary Wortley Montagu, who four years later introduced the practice to England.[13]
An account from letter by Lady Mary Wortley Montagu to Sarah Chiswell, dated 1 April 1717, from the Turkish Embassy describes this treatment:
The small-pox so fatal and so general amongst us is here entirely harmless by the invention of ingrafting (which is the term they give it). There is a set of old women who make it their business to perform the operation. Every autumn in the month of September, when the great heat is abated, people send to one another to know if any of their family has a mind to have the small-pox. They make parties for this purpose, and when they are met (commonly fifteen or sixteen together) the old woman comes with a nutshell full of the matter of the best sort of small-pox and asks what veins you please to have opened. She immediately rips open that you offer to her with a large needle (which gives you no more pain than a common scratch) and puts into the vein as much venom as can lye upon the head of her needle, and after binds up the little wound with a hollow bit of shell, and in this manner opens four or five veins. . . . The children or young patients play together all the rest of the day and are in perfect health till the eighth. Then the fever begins to seize them and they keep their beds two days, very seldom three. They have very rarely above twenty or thirty in their faces, which never mark, and in eight days time they are as well as before the illness. . . . There is no example of any one that has died in it, and you may believe I am very well satisfied of the safety of the experiment since I intend to try it on my dear little son. I am patriot enough to take pains to bring this useful invention into fashion in England, and I should not fail to write to some of our doctors very particularly about it if I knew any one of them that I thought had virtue enough to destroy such a considerable branch of their revenue for the good of mankind, but that distemper is too beneficial to them not to expose to all their resentment the hardy wight that should undertake to put an end to it. Perhaps if I live to return I may, however, have courage to war with them.[14]
In the early empirical days of vaccination, prior to Pasteur's work on establishing a germ theory and Lister's on antisepsis and asepsis there was considerable cross-infection. One of the early vaccinators is thought to have contaminated the cowpox matter—the vaccine—with smallpox matter (he worked in a smallpox hospital) and this produced essentially variolation. Other vaccine material was not reliably derived from Cowpox, but from other skin eruptions of cows[1]. In modern times an effective scientific model and controlled production were important in reducing these causes of apparent failure or iatrogenic illness.
Some of the earliest statistical and epidemiological studies were performed by James Jurin in 1727 and Daniel Bernoulli in 1766.[15]. Another early account was Dr Fewster's 1765 paper in the London Medical Society[16], entitled ""Cow pox and its ability to prevent smallpox"[17]. He reported that variolation induced no reaction in persons who had had cowpox[18]. Dr. Rolph, another Gloucestershire physician, stated that all experienced physicians of the time were aware of this[18].
At the age of thirteen, Jenner was apprenticed to Dr. Ludlow in Sodbury. He observed that people who caught cowpox while working with cows were known not to catch smallpox. He assumed a causal connection. The idea was not taken up by Dr. Ludlow at that time. After Jenner returned from medical school in London, a smallpox epidemic struck his home town of Berkeley, England. He advised the local cow workers to be inoculated. The farmers told him that cowpox prevented smallpox. This confirmed his childhood suspicion, and he studied cowpox further, presenting a paper on it to his local medical society.
Perhaps there was already an informal public understanding of some connection between disease resistance and working with cows. The “beautiful milkmaid” seems to have been a frequent image in the art and literature of this period. But we know for a fact: In the years following 1770 there were at least six people in England and Germany (Sevel, Jensen, Jesty 1774, Rendall, Plett 1791), who tested successfully the possibility of using the cowpox vaccine as an immunization for smallpox in humans. In 1796 Sarah Nelmes, a local milkmaid, contracted cowpox and went to Jenner for treatment. Jenner took the opportunity to test his theory. He inoculated James Phipps, the eight-year-old son of his gardener, not with smallpox but with cowpox. After an extremely weak bout of cowpox, James recovered. Jenner then tried to infect James with smallpox but nothing happened—the boy was immune to smallpox.
Jenner reported his observations to the Royal Society. Further work was suggested, and Jenner published a series of 23 cases, including his son Edward, none suffered severely from smallpox. Two years later a society to oppose vaccination had been established in Boston, Massachusetts[citation needed] — an indication of rapid spread and deep interest. By 1800 Jenner’s work had been published in all of the major European languages. The process was performed all over Europe and the United States. The death rate was close to zero with the process, which became known as vaccination and was continued to around 1974 in the UK. A typical death rate at that time was roughly one per million, making vaccination against smallpox with vaccinia the most dangerous immunisation widely provided in modern times.[citation needed] Thanks to the development of the smallpox vaccine, the disease was officially eradicated in 1979.
The Balmis Expedition (1803) carried the vaccine to Spanish America, the Philippines and China under commission of the Spanish Crown.
Some years before Dr. Jenner, Benjamin Jesty, a farmer at Yetminster in Dorset (he later moved to and is buried at Worth Matravers) is recorded as observing the two milkmaids living with his family to have been immune to smallpox and then inoculating his family with cowpox to protect them from smallpox. This was done in 1774 and can be found with Crookshank's History and Pathology of Vaccination, London 1889, vol. 1, p. 110ff. But the question of who first initiated smallpox inoculation/vaccination can not be answered properly, as there is in the sources the exact date and time only for the predecessor Plett (1791), but not for Sevel, Jensen and Rendall. Louis T. Wright,[19] an African-American and Harvard medical school graduate (1915), introduced intradermal vaccination for smallpox for the soldiers while serving in the Army during World War I.[20]
By 1977, smallpox, long considered to be the most deadly and persistent human pathogenic disease, was eradicated by the World Health Organization. This was accomplished through a massive, worldwide outbreak search and vaccination program. However, the variola virus that led to the death of 300 million in the 20th century alone was not completely exterminated with the disease it caused. Three known repositories of the virus were left, one in Birmingham, England which was later destroyed after an accidental escape from containment caused the death of Janet Parker, and two still remaining at the Centers for Disease Control in Atlanta, Georgia and the State Research Center of Virology and Biotechnology in Koltsovo, Russia. Each of those States reports that the repositories are retained for possible anti-bio-weaponry research and against the possibility that some obscure reservoir of natural smallpox may be discovered in the future.
It is important from the perspective of bioterrorism to note that some countries, including North Korea, did not participate in the WHO eradication program, choosing instead to mount their own program. There is no information at all to suggest that North Korea, which like many countries at the time was reported to have a bioweapons program, eliminated its samples of the virus.[21]
The vaccine consists of the virus which causes the related, yet far milder, cowpox disease; this virus is appropriately named vaccinia, from the Latin vacca which means cow. This vaccine has functional viruses in it which improves its effectiveness but, unfortunately, causes serious complications for people with impaired immune systems (for example chemotherapy and AIDS patients, and people with eczema) and is not yet considered safe for pregnant women. A woman planning on conceiving within one month should not receive the smallpox immunization until after the pregnancy. In the event of an outbreak the woman should delay pregnancy if possible. A small, yet significant, percentage of healthy individuals also suffer adverse side-effects which, in rare cases, include permanent neurological damage. Vaccines that only contain attenuated vaccinia viruses (an attenuated virus is one in which the pathogenicity has been decreased through serial passage) have been proposed but some researchers have questioned the possible effectiveness of such a vaccine. According to the Centers for Disease Control and Prevention (CDC), "vaccination within 3 days of exposure will prevent or significantly lessen the severity of smallpox symptoms in the vast majority of people. Vaccination 4 to 7 days after exposure likely offers some protection from disease or may modify the severity of disease." This, along with vaccinations of so-called first-responders, is the current plan of action being devised by the United States Department of Homeland Security (including Federal Emergency Management Agency (FEMA), now part of DHS) in the United States.
The vaccine can cause complications for those around those who are vaccinated. People who get the vaccine will shed virus particles through vesicles on their skin and possibly through their respiratory tract. Infections in close and not-so-close contacts can ensue. The current plan to vaccinate first responders has the potential to cause infection in the most vulnerable section of the population, the hospitalized ill. Family contacts are also susceptible, although they are less vulnerable because their immune systems are presumably intact. Secondary infection can cause skin disease, pulmonary disease and rarely, neurologic disease.
As of June 21, 2003, a scientific advisory panel had issued a recommendation against further vaccination of first responders because a significant number of those vaccinated suffered heart problems, notably pericarditis and myocarditis.
In May 2007, the Vaccines and Related Biological Products Advisory Committee of the U.S. Food and Drug Administration (FDA) voted unanimously that a new live virus vaccine produced by Acambis, ACAM2000, is both safe and effective for use in persons at high risk of exposure to smallpox virus. However, due to the high rate of serious adverse effects, the vaccine will only be made available to the CDC (a part of the United States Department of Health and Human Services) for the Strategic National Stockpile. [2] [3]
The main problem with developing a new, safer vaccine, is that, barring a bioterrorist attack on immunized individuals, its effectiveness cannot be tested on humans, and other animals do not naturally contract smallpox. Monkeys at USAMRIID research facilities have been infected, but tests on animals that are artificially infected with a human disease may give false or misleading results. To demonstrate safety and effectiveness, human trials always have to confirm data obtained from animal testing.
In the United States the smallpox vaccine is the only FDA-approved treatment for smallpox and monkeypox. As with smallpox, vaccination after infection is effective if the vaccine is given before symptoms develop.
Currently, the United States Air Force has made it mandatory that any Airman deploying to the Middle East must receive the smallpox vaccination before leaving stateside. The same is true of the U.S. Army, and any US Marine being deployed outside the contiguous United States (OCONUS), as well as any Marine or US Navy sailor being deployed ship side. It is also a requirement for all Department of Defense employees and contractors traveling to the United States Central Command's Area of Responsibility (CENTCOM AOR). [4]
In late 2001, the governments of the United States and the United Kingdom considered stockpiling smallpox vaccines, even while assuring the public that there was no "specific or credible" threat of bioterrorism.[22] Later, the director of State Research Center of Virology and Biotechnology VECTOR warned that terrorists could easily lure underpaid former Soviet researchers to turn over samples to be used as a weapon, saying "All you need is a sick fanatic to get to a populated place. The world health system is completely unprepared for this."[23]
In the United Kingdom, controversy erupted over the company contracted to supply the vaccine due to the political connections of its owner, Paul Drayson, and questions over the choice of vaccine strain being different from that used in the United States.[24] Plans for mass vaccinations in the United States stalled as the necessity and undesirable side-effects came into question.[25]
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