MMR vaccine

The MMR vaccine is a vaccine against measles, mumps, and rubella (German measles).[3] The first dose is generally given to children around 9 to 15 months of age, with a second dose at 15 months to 6 years of age, with at least 4 weeks between the doses.[4][5] After two doses, 97% of people are protected against measles, 88% against mumps, and at least 97% against rubella.[4] The vaccine is also recommended in those who do not have evidence of immunity,[4] those with well-controlled HIV/AIDS,[6][7] and within 72 hours of exposure to measles among those who are incompletely immunized.[5] It is given by injection.[4]

MMR vaccine
Mumps measles rubella vaccine
Combination of
Measles vaccineVaccine
Mumps vaccineVaccine
Rubella vaccineVaccine
Clinical data
Trade namesM-M-R II, Priorix, Tresivac, others
Other namesMPR vaccine[1]
AHFS/Drugs.comProfessional Drug Facts
MedlinePlusa601176
License data
Pregnancy
category
    ATC code
    Legal status
    Legal status
    • UK: POM (Prescription only)
    • US: ℞-only
    • In general: ℞ (Prescription only)
    Identifiers
    ChemSpider
    • none
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    The MMR vaccine is widely used around the world, with over 500 million doses having been given in over 100 countries as of 2001.[8][9] Measles resulted in 2.6 million deaths per year before immunization became common.[9] This has decreased to 122,000 deaths per year as of 2012, mostly in low-income countries.[9] Through vaccination, as of 2018, rates of measles in North and South America are very low.[9] Rates of disease have been seen to increase in populations which go unvaccinated.[9] Between 2000 and 2016, vaccination decreased measles deaths by a further 84%.[10]

    Side effects of immunization are generally mild and go away without any specific treatment.[11] These may include fever, and pain or redness at the injection site.[11] Severe allergic reactions occur in about one in a million people.[11] Because it contains live viruses, the MMR vaccine is not recommended during pregnancy, but may be given while breastfeeding.[4] The vaccine is safe to give at the same time as other vaccines.[11] Being recently immunized does not increase the risk of passing measles, mumps, or rubella on to others.[4] Vaccination does not increase the risk of autism.[12][13][14] The MMR vaccine is a mixture of live weakened viruses of the three diseases.[4]

    The MMR vaccine was developed by Maurice Hilleman.[3] It was licensed for use by Merck in 1971.[15] Stand-alone measles, mumps, and rubella vaccines had been previously licensed in 1963, 1967, and 1969 respectively.[15][16] Recommendations for a second dose were introduced in 1989.[15] The MMRV vaccine which also covers chickenpox may be used instead.[4] An MR vaccine, without coverage for mumps, is also occasionally used.[17]

    Medical use

    In 2020, Cochrane concluded "Existing evidence on the safety and effectiveness of MMR vaccine supports current policies of mass immunisation aimed at global measles eradication and in order to reduce morbidity and mortality associated with mumps and rubella."[12]

    The combined MMR vaccine induces immunity less painfully than three separate injections at the same time, and sooner and more efficiently than three injections given on different dates. Public Health England reports that providing a single combined vaccine as of 1988 rather than giving the option to have them also done separately increased uptake of the vaccine.[18]

    Measles
    Measles cases reported in the United States fell dramatically after introduction of the measles vaccine.

    Before the widespread use of a vaccine against measles, rates of disease were so high that infection was felt to be "as inevitable as death and taxes."[19] Reported cases of measles in the United States fell from hundreds of thousands to tens of thousands per year following introduction of the vaccine in 1963. Increasing uptake of the vaccine following outbreaks in 1971, and 1977, brought this down to thousands of cases per year in the 1980s. An outbreak of almost 30,000 cases in 1990 led to a renewed push for vaccination and the addition of a second vaccine to the recommended schedule. Fewer than 200 cases have been reported in the U.S. each year between 1997 and 2013, and the disease is no longer considered endemic there.[20][21][22]

    The benefit of measles vaccination in preventing illness, disability, and death has been well documented. The first 20 years of licensed measles vaccination in the U.S. prevented an estimated 52 million cases of the disease, 17,400 cases of intellectual disability, and 5,200 deaths.[23] During 1999–2004, a strategy led by the World Health Organization and UNICEF led to improvements in measles vaccination coverage that averted an estimated 1.4 million measles deaths worldwide.[24] Between 2000 and 2013, measles vaccination resulted in a 75% decrease in deaths from the disease.[25]

    Measles is common in many areas of the world. Although it was declared eliminated from the U.S. in 2000, high rates of vaccination and good communication with persons who refuse vaccination are needed to prevent outbreaks and sustain the elimination of measles in the U.S.[26] Of the 66 cases of measles reported in the U.S. in 2005, slightly over half were attributable to one unvaccinated individual who acquired measles during a visit to Romania.[27] This individual returned to a community with many unvaccinated children. The resulting outbreak infected 34 people, mostly children and virtually all unvaccinated; 9% were hospitalized, and the cost of containing the outbreak was estimated at $167,685. A major epidemic was averted due to high rates of vaccination in the surrounding communities.[26]

    In 2017, an outbreak of measles occurred among the Somali-American community in Minnesota, where MMR vaccination rates had declined due to the misconception that the vaccine could cause autism. The Centers for Disease Control and Prevention recorded 65 affected children in the outbreak by April 10, 2017.[28]

    Rubella
    Rubella rates fell sharply in the United States when immunization was introduced.

    Rubella, also known as German measles, was also very common before widespread vaccination. The major risk of rubella is during pregnancy when the baby may contract congenital rubella, which can cause significant congenital defects.[29]

    Mumps

    Mumps is another viral disease that was once very common, especially during childhood. If mumps is acquired by a male who is past puberty, a possible complication is bilateral orchitis, which can in some cases lead to sterility.[30]

    Administration

    The MMR vaccine is administered by a subcutaneous injection. The second dose may be given as early as one month after the first dose.[31] The second dose is a dose to produce immunity in the small number of persons (2–5%) who fail to develop measles immunity after the first dose. In the U.S. it is done before entry to kindergarten because that is a convenient time.[32] Areas where measles is common typically recommend the first dose at 9 months of age and the second dose at 15 months of age.[5]

    Safety

    Adverse reactions, rarely serious, may occur from each component of the MMR vaccine. Ten percent of children develop fever, malaise, and a rash 5–21 days after the first vaccination;[33] and 3% develop joint pain lasting 18 days on average.[34] Older women appear to be more at risk of joint pain, acute arthritis, and even (rarely) chronic arthritis.[35] Anaphylaxis is an extremely rare but serious allergic reaction to the vaccine.[36] One cause can be egg allergy.[37] In 2014, the FDA approved two additional possible adverse events on the vaccination label: acute disseminated encephalomyelitis (ADEM), and transverse myelitis, with permission to also add "difficulty walking" to the package inserts.[38] A 2012 IOM report found that the measles component of the MMR vaccine can cause measles inclusion body encephalitis in immunocompromised individuals. This report also rejected any connection between the MMR vaccine and autism.[39] Some versions of the vaccine contain the antibiotic neomycin and therefore should not be used in people allergic to this antibiotic.[14]

    The number of reports on neurological disorders is very small, other than evidence for an association between a form of the MMR vaccine containing the Urabe mumps strain and rare adverse events of aseptic meningitis, a form of viral meningitis.[35][40] The UK National Health Service stopped using the Urabe mumps strain in the early 1990s due to cases of transient mild viral meningitis, and switched to a form using the Jeryl Lynn mumps strain instead.[41] The Urabe strain remains in use in a number of countries; MMR with the Urabe strain is much cheaper to manufacture than with the Jeryl Lynn strain,[42] and a strain with higher efficacy along with a somewhat higher rate of mild side effects may still have the advantage of reduced incidence of overall adverse events.[41]

    A Cochrane review found that, compared with placebo, MMR vaccine was associated with fewer upper respiratory tract infections, more irritability, and a similar number of other adverse effects.[12]

    Naturally acquired measles often occurs with immune thrombocytopenic purpura (ITP, a purpuric rash and an increased tendency to bleed that resolves within two months in children). Approximately 1 in 40,000 children are thought to acquire ITP in the six weeks following an MMR vaccination, which is a higher rate than found in unvaccinated populations.[43] ITP below the age of six years is generally a mild disease, rarely having long-term consequences.[44][45]

    False claims about autism

    In 1998 Andrew Wakefield et al. published a fraudulent paper about twelve children, reportedly with bowel symptoms and autism or other disorders acquired soon after administration of MMR vaccine,[46] while supporting a competing vaccine. In 2010, Wakefield's research was found by the General Medical Council to have been "dishonest",[47] and The Lancet fully retracted the paper.[48] Three months following The Lancet's retraction, Wakefield was struck off the UK medical register, with a statement identifying deliberate falsification in the research published in The Lancet,[49] and was barred from practising medicine in the UK.[50] The research was declared fraudulent in 2011 by the British Medical Journal.[51]

    Peer-reviewed studies have failed to show any association between the vaccine and autism.[12][52] The Centers for Disease Control and Prevention,[53] the Institute of Medicine of the National Academy of Sciences,[54] the UK National Health Service[55] and the Cochrane Library review[12] have all concluded that there is no evidence of a link.

    Administering the vaccines in three separate doses does not reduce the chance of adverse effects, and it increases the opportunity for infection by the two diseases not immunized against first.[52][56] Health experts have criticized media reporting of the MMR-autism controversy for triggering a decline in vaccination rates.[57] Before publication of Wakefield's findings, the inoculation rate for MMR in the UK was 92%; after publication, the rate dropped to below 80%. In 1998, there were 56 measles cases in the UK; by 2008, there were 1348 cases, with two confirmed deaths.[58]

    In Japan, the MMR triplet is not used. Immunity is achieved by a combination vaccine for measles and rubella, followed up later with a mumps only vaccine. This has had no effect on autism rates in the country, further disproving the MMR autism hypothesis.[59]

    History
    Maurice Hilleman, who developed the MMR vaccine
    Two workers make openings in chicken eggs in preparation for a measles vaccine

    The component viral strains of MMR vaccine were developed by propagation in animal and human cells as all viruses require a living host cell to replicate.

    For example, in the case of mumps and measles viruses, the virus strains were grown in embryonated chicken eggs. This produced strains of virus which were adapted for chicken cells and less well-suited for human cells. These strains are therefore called attenuated strains. They are sometimes referred to as neuroattenuated because these strains are less virulent to human neurons than the wild strains.

    The Rubella component, Meruvax, was developed in 1967 through propagation using the human embryonic lung cell line WI-38 (named for the Wistar Institute) that was derived six years earlier in 1961.[60][61]

    Disease immunized Component vaccine Virus strain Propagation medium Growth medium
    Measles Attenuvax Enders' attenuated Edmonston strain[62] chick embryo cell culture Medium 199
    Mumps Mumpsvax[63] Jeryl Lynn (B level) strain[64]
    Rubella Meruvax II Wistar RA 27/3 strain of live attenuated rubella virus WI-38 human embryonic cell line MEM (solution containing buffered salts, fetal bovine serum, human serum albumin and neomycin, etc.)

    MMR II is supplied freeze-dried (lyophilized) and contains live viruses. Before injection it is reconstituted with the solvent provided.

    The term "MPR vaccine" is based on the Latin names of the diseases.

    The MMR vaccine Pluserix (known as Trivirix in Canada) uses the Urabe mumps strain. It is no longer used in the UK or Canada, but it remains in use in a number of countries.[65]

    MMRV vaccine
    Main article: MMRV vaccine

    The MMRV vaccine, a combined measles, mumps, rubella and varicella (chickenpox) vaccine, has been proposed as a replacement for the MMR vaccine to simplify administration of the vaccines.[31] Preliminary data indicate a rate of febrile seizures of 9 per 10,000 vaccinations with MMRV, as opposed to 4 per 10,000 for separate MMR and varicella shots; U.S. health officials therefore do not express a preference for use of MMRV vaccine over separate injections.[66]

    In a 2012 study[67] pediatricians and family doctors were sent a survey to gauge their awareness of the increased risk of febrile seizures (fever fits) in the MMRV. 74% of family doctors and 29% of pediatricians were unaware of the increased risk of febrile seizures. After reading an informational statement only 7% of family doctors and 20% of pediatricians would recommend the MMRV for a healthy 12- to 15-month-old child. The factor that was reported as the "most important" deciding factor in recommending the MMRV over the MMR+V was ACIP/AAFP/AAP recommendations (pediatricians, 77%; family physicians, 73%).

    MR vaccine

    This is a vaccine that covers measles and rubella but not mumps.[17] It is used in a few areas of the world as of 2014.[17]

    Religious concerns

    Some brands of this vaccine use gelatine, derived from domestic pigs, as a stabilizer. This has caused reduced take-up, and consequent increased levels of disease, among communities with a high proportion of Muslims or Orthodox Jews.[68][69]

    gollark: Never mind, I don't think I even have the RAM to store the final result of 9^9^9.
    gollark: I wonder if they use an efficient™ exponentiation algorithm.
    gollark: Since even 9^9^9 takes measurable time, good luck.
    gollark: It appears to be using a core trying to find out.
    gollark: Neither can my python interpretoid.

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    Further reading
    • World Health Organization (January 2009). The immunological basis for immunization series: module 7: measles (update 2009). World Health Organization (WHO). hdl:10665/44038. ISBN 9789241597555.
    • World Health Organization (November 2010). The immunological basis for immunization series: module 16: mumps. World Health Organization (WHO). hdl:10665/97885. ISBN 9789241500661.
    • World Health Organization (December 2008). The immunological basis for immunization series: module 11: rubella. World Health Organization (WHO). hdl:10665/43922. ISBN 9789241596848.
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