The Australian Immunisation Handbook 10th Edition
This chapter has been amended on July 2016.
- 4.23.1 - Virology
- 4.23.2 - Clinical features
- 4.23.3 - Epidemiology
- 4.23.4 - Vaccines
- 4.23.5 - Transport, storage and handling
- 4.23.6 - Dosage and administration
- 4.23.7 - Recommendations
- 4.23.8 - Pregnancy and breastfeeding
- 4.23.9 - Contraindications
- 4.23.10 - Precautions
- 4.23.11 - Adverse events
- 4.23.12 - Public health management of yellow fever
- 4.23.13 - Variations from product information
Yellow fever is a viral haemorrhagic fever caused by an RNA flavivirus. The virus is transmitted by mosquitoes (predominantly Ae.aegypti) through jungle (between non-human primates and mosquitoes) and urban (between humans and mosquitoes) zoonotic transmission cycles. In Africa, an intermediate transmission cycle exists between humans or non-human primates and Aedes species mosquitoes that breed in tree holes in savannah areas.1
The clinical spectrum of yellow fever varies from a non-specific febrile illness to fatal haemorrhagic fever.2 After an incubation period of 3 to 6 days, the disease begins abruptly with fever, prostration, myalgia and headache. The patient appears acutely ill with congestion of the conjunctivae; there is an intense viraemia during this ‘period of infection’, which lasts 3 to 4 days.2 This may be followed by the ‘period of remission’, in which the fever and symptoms settle over 24 to 48 hours, during which the virus is cleared by immune responses.2
Approximately 15 to 25% of patients may then relapse with a high fever, vomiting, epigastric pain, jaundice, renal failure and haemorrhage, referred to as ‘the period of intoxication’.2 These complications can be severe, and reflect the viscerotropic nature of the yellow fever virus (its ability to infect the liver, heart and kidneys). The case-fatality rate varies widely, but can be more than 20% in local populations.3
Yellow fever virus occurs in tropical and subtropical regions of Africa and South America where it is endemic and intermittently epidemic.
The epidemiology of yellow fever is dynamic due to changes in climate, such as rainfall patterns, and human factors such as migration and air travel.1 West Africa has the highest burden of yellow fever disease, accounting for 90% of all yellow fever cases reported between 1985 and 2009. The remainder of cases occur in other regions of Africa and South America.4 In 2014, 21 cases of yellow fever, including 12 deaths, were reported to the World Health Organization (WHO) from three countries: the Democratic Republic of Congo, Brazil and Peru. In 2006, the WHO introduced the Yellow Fever Initiative with the aim to control and eliminate epidemic yellow fever in Africa by including yellow fever vaccine in routine childhood immunisation programs and implementing mass vaccination campaigns. In endemic areas where high vaccination coverage has been achieved, the occurrence of yellow fever outbreaks has decreased substantially. A similar approach has been taken in South America.5
The risk of susceptible travellers acquiring yellow fever varies considerably with season, location, duration of travel and utilisation of mosquito avoidance measures. There have been reported cases of yellow fever, all fatal, in unvaccinated travellers to Africa and South America.6 Updated information regarding yellow fever virus activity and/or risk in travel destinations should be sought from a reputable source prior to travel (for example, Health information for international travel (the ‘Yellow book’) published by the US Centers for Disease Control and Prevention, available at (www.cdc.gov/travel/yellowbook)).7
- Stamaril – Sanofi-Aventis Australia Pty Ltd (live attenuated yellow fever virus (17D strain)). Lyophilised powder in a monodose vial with a pre-filled diluent syringe. Each 0.5 mL reconstituted dose contains ≥1000 IU of yellow fever virus; 16.0 mg lactose; 8.0 mg sorbitol; 0.833 mg L-histidine hydrochloride. May contain traces of egg proteins.
Yellow fever vaccine is a live, freeze-dried preparation of attenuated 17D strain yellow fever virus cultured in, and harvested from, embryonated chicken eggs. The vaccine does not contain antibiotics, preservatives or gelatin.
There are no studies that directly assess the efficacy of yellow fever vaccine. However, immunogenicity is used as a surrogate for protection, with thresholds for protective immunity defined as either log10 neutralisation index (LNI) >0.7, or a titre of >1:10 using plaque reduction neutralisation tests.8 Following a single dose of yellow fever vaccine, protective levels of neutralising antibodies are achieved in approximately 90% of healthy adult vaccine recipients by day 14, and in virtually all recipients by day 28.4 In children, the proportion of vaccine recipients who achieve protective yellow fever antibody levels following a single dose of vaccine is similar to that in adults.9,10 One randomised trial suggested lower seroconversion rates against yellow fever virus in children <2 years of age (70%); however, this was when yellow fever vaccine was co-administered with MMR vaccine.11 In comparison, 87% of children who received yellow fever and MMR vaccines separated by an interval of 30 days or more seroconverted. This study did not report on the proportion of participants with protective levels of neutralising antibodies based on commonly applied definitions.
Immunogenicity studies in individuals with underlying medical conditions are limited. Some data suggest that pregnant women and HIV-infected persons do not respond optimally to yellow fever vaccination. The proportion of recipients who achieved protective levels of neutralising antibodies was lower in women who received yellow fever vaccine in their third trimester of pregnancy (38.6%) than in non-pregnant women of child-bearing age and other adults (81.5–93.7%).12 However, a better response to the yellow fever vaccine was reported in a separate study of women vaccinated in their first trimester of pregnancy, suggesting that antibody response to vaccination in pregnant women may be dependent on length of gestation.13 Two studies reported lower rates of neutralising antibodies among HIV-infected persons compared with uninfected controls.14,15 Although some observational studies have reported seroconversion rates in HIV-infected persons similar to those reported in healthy adults (>90%), the number of participants in these studies was small and there were no healthy controls.16-19 When reported, CD4+ counts of HIV-infected subjects were >200 cells per µL. A number of studies found higher antibody titres were associated with higher CD4+ counts and lower HIV RNA levels.19,20
Data on the immunogenicity of yellow fever vaccine in persons who are immunocompromised, other than with HIV infection, is limited to a few small low quality studies and case reports.21,22 A reduced immune response to yellow fever vaccine has been reported among persons receiving immunosuppressive therapy for rheumatoid disease.23
Immunity to yellow fever virus following a single dose of yellow fever vaccine is expected to be life-long in the majority of healthy vaccine recipients. Protective levels of neutralising antibodies have been detected in 75 to 100% of healthy adults from endemic and non-endemic yellow fever areas when measured ≥10 years after primary immunisation (ranging from 10 to 69 years post vaccination).24-26 Since the 1930s, more than 540 million doses of yellow fever vaccine have been administered with only 12 suspected cases of yellow fever disease identified among vaccine recipients. All 12 cases developed symptoms within 5 years of vaccination, suggesting primary vaccine failure (poor initial immune response) rather than secondary vaccine failure due to waning immunity.27
There are few studies which have assessed the duration of immunity in groups who do not respond optimally to primary yellow fever vaccination. A cohort study of HIV-infected individuals that measured yellow fever neutralising antibodies over many years reported 23% of patients lost protective levels of neutralising antibody within 1 to 10 years of vaccination, almost twice the proportion among HIV-uninfected individuals (12%).15
A booster dose of yellow fever vaccine has been shown to be effective in producing protective levels of yellow fever neutralising antibodies in those whose response to their primary vaccine dose was low or negative.28,29
Transport according to National vaccine storage guidelines: Strive for 5.30 Store at +2°C to +8°C. Do not freeze. Protect from light.
Stamaril must be reconstituted by adding the entire contents of the diluent syringe to the vial and shaking until the powder is completely dissolved. Reconstituted vaccine must be used within 1 hour.
The dose of yellow fever vaccine for children and adults is 0.5 mL, to be given by either IM or SC injection.
Co-administration with other vaccines
Inactivated vaccines and oral live vaccines relevant to travel (e.g. cholera, typhoid) can be given with, or at any time before or after, yellow fever vaccine.
If administration of both yellow fever and other parenteral live vaccines is indicated, the vaccines can be given either on the same day or at least 4 weeks apart. Studies of yellow fever vaccine administered at the same time as other live vaccines, including Japanese encephalitis,31 BCG and monovalent measles vaccines,27 have shown no impact on the immune response to any of the vaccine antigens. Although one Brazilian study suggested the co-administration of yellow fever and MMR vaccines results in lower seroconversion rates to the vaccine antigens than when the vaccines are administered at least 4 weeks apart (refer to 4.23.4 Vaccine above), further studies are required to determine the clinical significance of this finding. Yellow fever vaccine can be given at the same time as the Imojev Japanese encephalitis vaccine,31 using separate syringes and separate injection sites.
Children aged <9 months
Yellow fever vaccine is contraindicated in infants aged <9 months (refer to 4.23.9 Contraindications below).
Children aged ≥9 months and adults
Yellow fever vaccination can only be provided at Yellow Fever Vaccination Centres approved by the relevant state or territory health authorities (refer to ‘International travel requirements’ below).
A single dose of yellow fever vaccine is recommended for:
- persons ≥9 months of age travelling to, or living in, an area with a risk of yellow fever virus transmission. Information about the risk for specific destinations should be sought from a reputable source, such as the WHO32 or the Centers for Disease Control and Prevention,7 prior to travel.
- laboratory personnel who routinely work with yellow fever virus.
Vaccination is generally not recommended when travelling to an area where there is low potential for yellow fever virus exposure (i.e. no human yellow fever cases ever reported and evidence to suggest only low levels of yellow fever virus transmission in the past).
However, vaccination may be considered for travellers outside of the above groups under certain circumstances, for example, to meet specific countries’ vaccination requirements for travel (refer to ‘International travel requirements’ below).
In most individuals, a booster dose is not required as a single dose of yellow fever vaccine induces protective antibody levels that persist for many decades (refer to 4.23.4 Vaccine above).
A booster dose is recommended for those individuals who do not respond optimally to yellow fever vaccination (refer to 4.23.4 Vaccine above) if they are travelling to, or living in, an area with a risk of yellow fever virus transmission and 10 or more years have passed since their last dose. These individuals include:
- women who were pregnant when they received their initial dose of yellow fever vaccine, regardless of trimester
- persons who were infected with HIV when they received their initial dose of yellow fever vaccine (regardless of their degree of immunosuppression at the time).
A booster dose may be considered for travellers outside of the above groups under certain circumstances, for example, to meet specific countries’ vaccination requirements for travel (refer to ‘International travel requirements’ below) or due to a higher risk of yellow fever virus infection (e.g. if living in a high-risk location for an extended period of time or travelling to an area with ongoing outbreaks).
Laboratory workers with ongoing exposure to yellow fever virus should have neutralising antibody titres measured if 10 years or more have passed since their last vaccine dose to determine if a protective antibody level has been maintained. If antibody titres cannot be measured, a booster dose should be administered every 10 years.
Individuals who received a haematopoietic stem cell transplant after a dose of yellow fever vaccine should receive an additional vaccine dose prior to the next time they will be at risk of yellow fever virus infection, irrespective of the period since their last dose. The additional dose should preferably be administered after a period of 24 months has elapsed following the transplant. If the patient has ongoing graft-versus-host disease or remains on immunosuppressive therapy, vaccination should be delayed until the patient is sufficiently immunocompetent. (Refer also to 3.3.3 Vaccination of immunocompromised persons, ‘Haematopoietic stem cell transplant recipients’.)
International travel requirements
All those travelling to, or living in, countries with a risk of yellow fever virus transmission should be informed that the mosquito vectors of yellow fever usually bite during the day. They should be advised of the necessity for mosquito avoidance measures, even if vaccinated. These include the use of insect repellents, coils and sprays, the use of mosquito nets (preferably those that have been treated with an insecticide), and adequate screening of residential and work premises.
Under the International Health Regulations (2005) (IHR), many countries require travellers arriving from countries with a risk of yellow fever virus transmission to provide a valid International Certificate of Vaccination or Prophylaxis (ICVP) against yellow fever, or a valid letter of exemption, prior to entry. A country may require such documentation even for travellers who are only in transit through that country. This is because importation of the virus into these countries by an infected traveller could result in introduction and establishment of the virus in local Ae. aegypti mosquitoes. In 2014, the World Health Assembly of the WHO agreed to extend the validity of the ICVP from 10 years to the duration of the life of the vaccinated person, based on evidence demonstrating that a single dose of yellow fever vaccine provides protection for many decades in most individuals (refer to 4.23.4 Vaccine above). This change in the IHR took effect in June 2016 but yellow fever vaccination entry requirements for some countries may still vary.
It is recommended that the entry requirements for yellow fever vaccination for the countries a traveller intends to enter or transit through be confirmed prior to travel by contacting the country’s foreign missions in Australia.
Australia’s travel requirements
Australia strongly recommends that travellers >1 year of age entering Australia within 6 days of leaving a country on Australia’s list of yellow fever declared places, where they have stayed overnight or longer, have a valid ICVP with proof of valid yellow fever vaccination. Yellow fever vaccination and an ICVP can only be issued by accredited Yellow Fever Vaccination Centres approved by the relevant state or territory health authorities. The ICVP must record the name of the vaccinated individual, date of the vaccination (day–month–year sequence, with the month written in letters), the vaccine administered, the signature of the authorised health professional and the official stamp provided by the state or territory health authority.
Australia has adopted the WHO amendment to the IHR and as such, as of 16 June 2016, an ICVP is considered valid for the duration of the life of the vaccinated person. The certificate becomes valid 10 days after vaccination.
Travellers who do not have a valid certificate are provided with information on yellow fever and are recommended to promptly seek medical assessment if they develop relevant symptoms within 6 days of leaving a yellow fever declared place. A list of yellow fever declared places is available from the Australian Government Department of Health’s yellow fever fact sheet.
Exemptions to vaccination
People with a true contraindication to yellow fever vaccine (refer to 4.23.9 Contraindications below) who intend to travel to countries with a risk of yellow fever virus transmission should obtain a dated and signed letter on letterhead stationery from an accredited Yellow Fever Vaccination Centre. The letter should clearly state the yellow fever vaccine is contraindicated on medical grounds and display the centre’s official stamp provided by the state or territory health authority. Medical exemption letters should be written for the current trip only. If exemption to yellow fever vaccination is required for any subsequent trips, a new medical exemption letter should be issued. The vaccination provider is also required to complete, stamp and sign the Medical Contraindications to Vaccination section of the ICVP. Arriving travellers who possess a medical exemption letter for yellow fever vaccination are provided with information on yellow fever and recommended to promptly seek medical assessment if they develop relevant symptoms.
If it is expected that the exemption to yellow fever vaccination will be required in another country where travel is planned, the traveller should contact the country’s foreign missions in Australia to ascertain if the letter needs to be in another language in addition to English.
Yellow fever vaccine is not recommended for pregnant women or for women breastfeeding infants aged <9 months, other than in exceptional circumstances.
As with all live attenuated virus vaccines, yellow fever vaccine should not routinely be given to pregnant women, unless there is a risk of exposure to the virus. Pregnant women should be advised against going to an area with a risk of yellow fever virus transmission. However, where travel to an at-risk area is unavoidable, such women should be vaccinated.13,33-35 Women who received their first dose of yellow fever vaccine while pregnant may require additional doses in the future if they remain at risk of yellow fever virus transmission (refer to 4.23.7 Recommendations above).
The yellow fever vaccine has been given to considerable numbers of pregnant women4,13,33 with no evidence of any adverse outcomes. Therefore, women vaccinated in early pregnancy can be reassured that there is no evidence of risk to themselves and very low (if any) risk to the fetus.4
Administration of yellow fever vaccine to women who are breastfeeding infants aged <9 months should be avoided, except in situations where exposure to yellow fever virus cannot be avoided or postponed.34,35 Although extremely rare, there have been several case reports of transmission of the vaccine strain of yellow fever virus via breast milk resulting in probable vaccine-associated neurotropic disease in the infants (refer to 4.23.11 Adverse events below). On follow-up of these infants, their neurological development was considered normal.34,35
Refer to 3.3 Groups with special vaccination requirements, Table 3.3.1 Recommendations for vaccination in pregnancy for more information.
Any person with a true contraindication to yellow fever vaccination should be advised against going to an area with a risk of yellow fever virus transmission. However, where travel to an at-risk area is unavoidable, such persons should be advised of the necessity for mosquito avoidance measures (refer to 4.23.7 Recommendations, ‘International travel requirements’ above).
Anaphylaxis to vaccine components
Yellow fever vaccine is contraindicated in persons who have had:
- anaphylaxis following a previous dose of the vaccine
- anaphylaxis following any vaccine component.
In particular, the vaccine is contraindicated in persons with a known anaphylaxis to eggs. Persons with a known allergy to eggs wishing to receive yellow fever vaccination should discuss this with either an immunologist/allergist or be referred to a specialised immunisation adverse events clinic. Contact a specialist travel medicine clinic or your local state or territory health authority for further details (refer to Appendix 1 Contact details for Australian, state and territory government health authorities and communicable disease control).
Routine yellow fever vaccine is generally contraindicated in infants <9 months of age due to the risk of severe adverse events following vaccination (refer to 4.23.11 Adverse events below). However, countries experiencing a mass outbreak of yellow fever may elect to immunise infants from as young as 6 months of age.36
Persons who are immunocompromised
As with all live viral vaccines, the yellow fever vaccine should generally not be given to people who are immunocompromised due to either disease or medical treatment. The vaccine can, however, be considered on a case-by-case basis taking into account factors such as risk of exposure and level of compromise (refer to3.3.3 Vaccination of immunocompromised persons). There is a concern that immunocompromised individuals may not mount a sufficient immune response following vaccination and may be at risk of vaccine-related adverse events. However, there are few studies assessing yellow fever vaccine immunogenicity in these individuals (refer to 4.23.4 Vaccine above) and an association with serious adverse events has only been demonstrated for individuals with thymus disorders (refer to 4.23.11 Adverse events below).
Yellow fever vaccine can be given to certain persons infected with HIV who are at risk of yellow fever virus infection (refer to 4.23.10 Precautions below).
People with a history of any thymus disorder, including myasthenia gravis, thymoma, thymectomy and DiGeorge syndrome, or thymic damage from chemoradiotherapy or graft-versus-host disease, should not be given the yellow fever vaccine due to the increased risk of yellow fever vaccine-associated viscerotropic disease37 (refer to 4.23.11 Adverse events below).
Adults aged ≥60 years
The risk of severe adverse events following yellow fever vaccine is greater in those aged ≥60 years than in younger adults.38-42
Adults ≥60 years of age should be given yellow fever vaccine only if they intend to travel to endemic countries (as recommended above) and they have been informed about the (albeit very low) risks of developing a severe complication.
Yellow fever vaccine can be administered to HIV-infected persons who are at risk of yellow fever virus infection, providing they are not immunocompromised (refer to 3.3.3 Vaccination of immunocompromised persons). Studies of yellow fever vaccine in small numbers of HIV-infected participants suggest a reduced immune response, but vaccination is well tolerated14,15 (refer to 4.23.4 Vaccine above).
There are few studies of yellow fever vaccine in HIV-infected persons with CD4+ counts <200 per µL and a decision to vaccinate such persons where risk of yellow fever infection is unavoidable should be considered on a case-by-case basis.
Mild adverse events
Adverse events following yellow fever vaccine are generally mild. Vaccine recipients often report mild headaches, myalgia and low-grade fevers or other minor symptoms in the first 5 days after vaccination, which can last up to 2 weeks43. In clinical trials in which symptoms are actively elicited, up to 25% of vaccine recipients report mild adverse events and up to 1% curtail regular activities.4, 41,< a href="#44">44
Immediate hypersensitivity reactions
Immediate hypersensitivity reactions, including anaphylaxis, following yellow fever vaccine are very rare, with an incidence of less than 1 in 1 million, and occur principally in people with anaphylactic sensitivity to eggs.4,41,44 Although it has been suggested that an anaphylactic sensitivity to gelatin (added as a stabiliser to some yellow fever vaccines) may also precipitate anaphylaxis following vaccination,45 Stamaril does not contain gelatin.
Vaccine-associated neurotropic adverse events
Yellow fever vaccine-associated neurotropic disease (YF-AND) is a severe adverse event that is rarely fatal. YF-AND manifests as several distinct clinical syndromes, including meningoencephalitis (neurotropic disease), Guillain-Barré syndrome, acute disseminated encephalomyelitis and bulbar palsy.46,47 Between 1989 and March 2011, 113 cases of neurological adverse events following yellow fever vaccination were reported worldwide.4
YF-AND is more likely to occur in very young infants and the elderly. Of 23 cases of meningoencephalitis reported between 1945 and 2001, 16 (70%) were infants <9 months of age with the majority <4 months of age. Recommendations made in the 1960s against immunisation of infants aged <6 months led to a reduction in the number of reports.48,49 Although YF-AND is rare in adults overall, the risk among adults is greatest in persons ≥60 years of age.38,40,50
Vaccine-associated viscerotropic adverse events
Yellow fever vaccine-associated viscerotropic disease (YF-AVD), characterised by multi-organ system failure, is a recognised rare (3–4 cases per million doses of vaccine) but severe adverse event following yellow fever vaccination. YF-AVD mimics naturally acquired yellow fever disease, with the vaccine virus proliferating and disseminating throughout the host’s tissues.51
Two risk factors have been identified for YF-AVD: older age and a history of thymus disease or thymectomy. A systematic review of YF-AVD among the elderly completed by the WHO found evidence to support an increased risk of YF-AVD among elderly travellers, though the risk among the elderly in endemic populations is undetermined.42 Four of the initial 27 reported cases of YF-AVD worldwide occurred in persons who had thymectomies performed for thymomas,37 a condition with a low prevalence in the general population.37,52
A number of cases of YF-AVD have involved a history of autoimmune disease or diseases with potential autoimmune aetiology. However, in a number of these cases, the individual also had another known risk factor. More information is needed to inform whether there is a greater risk of YF-AVD in persons with autoimmune disease.53
Yellow fever is a notifiable and quarantinable disease in all states and territories in Australia.
Further instructions about the public health management of yellow fever, including management of cases of yellow fever and their contacts, should be obtained from state/territory public health authorities (refer to Appendix 1 Contact details for Australian, state and territory government health authorities and communicable disease control).
The product information states that pregnancy is a contraindication to the yellow fever vaccine. The ATAGI recommends instead that pregnant women can be vaccinated where travel to an area with a risk of yellow fever virus transmission is unavoidable.
- Jentes ES, Poumerol G, Gershman MD, et al. The revised global yellow fever risk map and recommendations for vaccination, 2010: consensus of the Informal WHO Working Group on Geographic Risk for Yellow Fever. The Lancet Infectious Diseases 2011;11:622-32.
- Monath TP. Yellow fever: an update. The Lancet Infectious Diseases 2001;1:11-20.
- World Health Organization (WHO). Yellow fever fact sheet (revised in December 2009). Weekly Epidemiological Record 2010;85:33-6.
- Monath TP, Gershman M, Staples JE, Barrett AD. Yellow fever vaccine. In: Plotkin SA, Orenstein WA, Offit PA, eds. Vaccines. 6th ed. Philadelphia, PA: Elsevier Saunders 2013.
- Yactayo S, Ramón P, Luce R, Millot V. Yellow fever in Africa and the Americas, 2014. Weekly Epidemiological Record 2015;90:323-34.
- Monath TP, Cetron MS. Prevention of yellow fever in persons traveling to the tropics. Clinical Infectious Diseases 2002;34:1369-78.
- Gershman MD, Staples JE. Infectious diseases related to travel. Yellow fever. In: CDC Health information for international travel 2016: the Yellow Book. New York: Oxford University Press, 2016. Available at: (www.cdc.gov/travel) (accessed Jan 2016).
- Gotuzzo E, Yactayo S, Córdova E. Efficacy and duration of immunity after yellow fever vaccination: systematic review on the need for a booster every 10 years. American Journal of Tropical Medicine and Hygiene 2013;89:434-44.
- Belmusto-Worn VE, Sanchez JL, McCarthy K, et al. Randomized, double-blind, phase III, pivotal field trial of the comparative immunogenicity, safety, and tolerability of two yellow fever 17D vaccines (Arilvax™ and YF-VAX®) in healthy infants and children in Peru. American Journal of Tropical Medicine and Hygiene 2005;72:189-97.
- Osei-Kwasi M, Dunyo SK, Koram KA, et al. Antibody response to 17D yellow fever vaccine in Ghanaian infants. Bulletin of the World Health Organization 2001;79:1056-9.
- Nascimento Silva JR, Camacho LA, Siqueira MM, et al. Mutual interference on the immune response to yellow fever vaccine and a combined vaccine against measles, mumps and rubella. Vaccine 2011;29:6327-34.
- Nasidi A, Monath TP, Vandenberg J, et al. Yellow fever vaccination and pregnancy: a four-year prospective study. Transactions of the Royal Society of Tropical Medicine and Hygiene 1993;87:337-9.
- Suzano CE, Amaral E, Sato HK, Papaiordanou PM, Campinas Group on Yellow Fever Immunization during Pregnancy. The effects of yellow fever immunization (17DD) inadvertently used in early pregnancy during a mass campaign in Brazil. Vaccine 2006;24:1421-6.
- Sibailly TS, Wiktor SZ, Tsai TF, et al. Poor antibody response to yellow fever vaccination in children infected with human immunodeficiency virus type 1. Pediatric Infectious Disease Journal 1997;16:1177-9.
- Veit O, Niedrig M, Chapuis-Taillard C, et al. Immunogenicity and safety of yellow fever vaccination for 102 HIV-infected patients. Clinical Infectious Diseases 2009;48:659-66.
- Receveur MC, Thiébaut R, Vedy S, et al. Yellow fever vaccination of human immunodeficiency virus-infected patients: report of 2 cases. Clinical Infectious Diseases 2000;31:e7-8.
- Tattevin P, Depatureaux AG, Chapplain JM, et al. Yellow fever vaccine is safe and effective in HIV-infected patients. AIDS 2004;18:825-7.
- Pistone T, Verdière CH, Receveur MC, et al. Immunogenicity and tolerability of yellow fever vaccination in 23 French HIV-infected patients. Current HIV Research 2010;8:461-6.
- Sidibe M, Yactayo S, Kalle A, et al. Immunogenicity and safety of yellow fever vaccine among 115 HIV-infected patients after a preventive immunisation campaign in Mali. Transactions of the Royal Society of Tropical Medicine and Hygiene 2012;106:437-44.
- Pacanowski J, Lacombe K, Campa P, et al. Plasma HIV-RNA is the key determinant of long-term antibody persistence after yellow fever immunization in a cohort of 364 HIV-infected patients. Journal of Acquired Immune Deficiency Syndromes 2012;59:360-7.
- Kernéis S, Launay O, Ancelle T, et al. Safety and immunogenicity of yellow fever 17D vaccine in adults receiving systemic corticosteroid therapy: an observational cohort study. Arthritis Care and Research 2013;65:1522-8.
- Scheinberg M, Guedes-Barbosa LS, Mangueira C, et al. Yellow fever revaccination during infliximab therapy. Arthritis Care and Research 2010;62:896-8.
- Oliveira AC, Mota LM, Santos-Neto LL, et al. Seroconversion in patients with rheumatic diseases treated with immunomodulators or immunosuppressants, who were inadvertently revaccinated against yellow fever. Arthritis and Rheumatology 2015;67:582-3.
- de Melo AB, da Silva MP, Magalhães MC, et al. Description of a prospective 17DD yellow fever vaccine cohort in Recife, Brazil. American Journal of Tropical Medicine and Hygiene 2011;85:739-47.
- Collaborative Group for Studies on Yellow Fever Vaccines. Duration of post-vaccination immunity against yellow fever in adults. Vaccine 2014;32:4977-84.
- Centers for Disease Control and Prevention (CDC), Advisory Committee on Immunization Practices (ACIP). Grading of recommendations, assessment, development, and evaluation (GRADE) for yellow fever vaccine booster doses. 2015. Available at: (www.cdc.gov/vaccines/acip/recs/grade/yf-vac-boost.html) (accessed Dec 2015).
- World Health Organization (WHO). Vaccines and vaccination against yellow fever: WHO position paper – June 2013. Weekly Epidemiological Record 2013;88:269-83.
- Hepburn MJ, Kortepeter MG, Pittman PR, et al. Neutralizing antibody response to booster vaccination with the 17d yellow fever vaccine. Vaccine 2006;24:2843-9.
- Omilabu SA, Adejumo JO, Olaleye OD, Fagbami AH, Baba SS. Yellow fever haemagglutination-inhibiting, neutralising and IgM antibodies in vaccinated and unvaccinated residents of Ibadan, Nigeria. Comparative Immunology, Microbiology and Infectious Diseases 1990;13:95-100.
- National vaccine storage guidelines: Strive for 5. 2nd ed. Canberra: Australian Government Department of Health and Ageing, 2013. Available at: (www.immunise.health.gov.au/internet/immunise/publishing.nsf/Content/IMM77-cnt) (accessed Jan 2016).
- Nasveld PE, Marjason J, Bennett S, et al. Concomitant or sequential administration of live attenuated Japanese encephalitis chimeric virus vaccine and yellow fever 17D vaccine: randomized double-blind phase II evaluation of safety and immunogenicity. Human Vaccines 2010;6:906-14.
- World Health Organization (WHO). International travel and health. Available at: (www.who.int/ith/en/) (accessed Jan 2016).
- Cavalcanti DP, Salomão MA, Lopez-Camelo J, Pessoto MA, Campinas Group of Yellow Fever Immunization during Pregnancy. Early exposure to yellow fever vaccine during pregnancy. Tropical Medicine and International Health 2007;12:833-7.
- Kuhn S, Twele-Montecinos L, MacDonald J, Webster P, Law B. Case report: Probable transmission of vaccine strain of yellow fever virus to an infant via breast milk. CMAJ Canadian Medical Association Journal 2011;183:E243-5.
- Centers for Disease Control and Prevention (CDC). Transmission of yellow fever vaccine virus through breast-feeding – Brazil, 2009. MMWR. Morbidity and Mortality Weekly Report 2010;59:130-2.
- Monath TP. Review of the risks and benefits of yellow fever vaccination including some new analyses. Expert Review of Vaccines 2012;11:427-48.
- Barwick Eidex R. History of thymoma and yellow fever vaccination [letter]. The Lancet 2004;364:936.
- Khromava AY, Barwick Eidex R, Weld LH, et al. Yellow fever vaccine: an updated assessment of advanced age as a risk factor for serious adverse events. Vaccine 2005;23:3256-63.
- Lawrence GL, Burgess MA, Kass RB. Age-related risk of adverse events following yellow fever vaccination in Australia. [erratum appears in Commun Dis Intell. 2004;28(3):348]. Communicable Diseases Intelligence 2004;28:244-8.
- Lindsey NP, Schroeder BA, Miller ER, et al. Adverse event reports following yellow fever vaccination. Vaccine 2008;26:6077-82.
- Domingo C, Niedrig M. Safety of 17D derived yellow fever vaccines. Expert Opinion on Drug Safety 2009;8:211-21.
- Rafferty E, Duclos P, Yactayo S, Schuster M. Risk of yellow fever vaccine-associated viscerotropic disease among the elderly: a systematic review. Vaccine 2013;31:5798-805.
- Monath TP, Nichols R, Archambault WT, et al. Comparative safety and immunogenicity of two yellow fever 17D vaccines (ARILVAX and YF-VAX) in a phase III multicenter, double-blind clinical trial. American Journal of Tropical Medicine and Hygiene 2002;66:533-41.
- Marfin AA, Barwick Eidex RS, Kozarsky PE, Cetron MS. Yellow fever and Japanese encephalitis vaccines: indications and complications. Infectious Disease Clinics of North America 2005;19:151-68.
- Kelso JM, Mootrey GT, Tsai TF. Anaphylaxis from yellow fever vaccine. Journal of Allergy and Clinical Immunology 1999;103:698-701.
- McMahon AW, Eidex RB, Marfin AA, et al. Neurologic disease associated with 17D-204 yellow fever vaccination: a report of 15 cases. Vaccine 2007;25:1727-34.
- Kitchener S. Viscerotropic and neurotropic disease following vaccination with the 17D yellow fever vaccine, ARILVAX®. Vaccine 2004;22:2103-5.
- Stuart G. Reactions following vaccination against yellow fever. In: Yellow fever vaccination. World Health Organization Monograph Series No. 30. Geneva: WHO, 1956.
- Yellow fever vaccine: recommendation of the US Public Health Service Advisory Committee on Immunization Practices. Annals of Internal Medicine 1969;71:365-7.
- Martin M, Weld LH, Tsai TF, et al. Advanced age a risk factor for illness temporally associated with yellow fever vaccination. Emerging Infectious Diseases 2001;7:945-51.
- Gershman MD, Staples JE, Bentsi-Enchill AD, et al. Viscerotropic disease: case definition and guidelines for collection, analysis, and presentation of immunization safety data. Vaccine 2012;30:5038-58.
- Thomas PA. The need for organization and collaboration: establishing a thymoma registry. Thoracic surgery clinics 2011;21:131-4.
- Centers for Disease Control and Prevention (CDC), Staples JE, Gershman M, Fischer M. Yellow fever vaccine: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. Recommendations and Reports 2010;59(RR-7):1-26.