Mem Inst Oswaldo Cruz, Rio de Janeiro, 113(8) August 2018
Perspective

Discrepancies in the evaluation of the safety of the human papillomavirus vaccine

Jorge L Cervantes+, Amy Hoanganh Doan

Texas Tech University Health Sciences Center, Paul L Foster School of Medicine, El Paso, TX, USA

DOI: 10.1590/0074-02760180063
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ABSTRACT

Despite being more than ten years since its introduction, global acceptance to the human papillomavirus (HPV) vaccine is still low. The immunogenetic background of the host, and HPV antigen recognition, are important in natural HPV infection, and should be taken into account in the understanding of adverse autoimmune reactions by the HPV vaccine in certain groups. There is no doubt of the benefit of vaccines in the reduction of the incidence of infectious diseases, and in the case of HPV, the prevention of persistent infection that would lead to cervical cancer. Side-effects, however, should be closely monitored and reported without any bias, to ensure that the benefits of vaccines outweigh the risks of adverse reactions. In this article we bring the attention on certain adverse effects of the vaccine against HPV that have not been well studied as they are not well defined. We also compare the different approaches on HPV vaccine policies regarding its adverse reactions in countries like Japan and Colombia, vs. the recommendations issued by the WHO.

The vaccine against the human papillomavirus (HPV) - HPV infection is the most common sexually transmitted viral infection. Several risk factors for HPV infection have been identified, and include genetic predisposition, immune status, co-infection with other sexually transmitted diseases, and smoking. Persistent infection with this virus is associated with squamous carcinoma of the cervix, oropharynx, anus, genitalia (vulva, vagina and penis), head, and neck. Approximately 90% of HPV infections resolve spontaneously through the immune system. Persistent infection with high-risk types 16 and 18 contributes to 20% and 50% of cervical cancers, respectively (Skeate et al. 2016 22 ). It is thus, not surprising that the first HPV vaccines were directed toward these genotypes (Muñoz et al. 2008 16 ). There are 13 other high risk genotypes, including 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73 and 82 (Skeate et al. 2016 22 ), whose presence in certain populations of Latin America (Cervantes et al. 2003 2 ), could explain the discrepancy between the prevalence of 16/18 genotypes and the incidence of cervical cancer. A newer nonavalent vaccine has been approved by the Food and Drug Administration (FDA) to account for infections by seven high-risk HPV genotypes (16, 18, 31, 33, 45, 52, and 58) (Kirby 2015 11 ), as the HPV vaccine does not provide protection against other types than those included in the vaccine.

Current HPV vaccines are based on virus-like particles, and are composed of self-assembled pentamers of the larger protein of the L1 capsid. HPV vaccines are prophylactic and are not therapeutic. The goal of prophylactic HPV vaccination is to avoid persistent infections that will progress to an invasive carcinoma. HPV vaccination would not be appropriate to elicit an anti-cancer response, since the tumor cells do not express significant levels of L1 protein. For treatment of cancers originating from HPV there is immunotherapy, which focuses on generating a cellular immune response against antigens associated with cellular transformation (Skeate et al. 2016 22 ). The HPV vaccine does not modify the cellular immunity that is responsible for eliminating the infected cells, rather it induces the production of antibodies against the L1 protein in blood. The two main HPV vaccines, Gardasil (Merck) and Cervarix (GSK), were approved in 2006 and in 2009, respectively, so it is still difficult to predict its long-term efficacy.

 

Rejection of the HPV vaccine - Even though more than 10 years have passed since its introduction, the global acceptance of the HPV vaccine remains low. In Latin America, the immunization rate is lower than expected (Tabakman 2017 24 ). In developed countries such as Canada, the rejection of HPV vaccination is high in both the lowest and the highest economic levels (Remes et al. 2014 20 ).

Several countries in Latin America have shown a marked decrease in their immunization rates (Tabakman 2017 24 ). The initial recommendation of three intramuscular doses has now been reduced to two doses in a period of 6 to 24 months, in order to reduce costs and increase compliance (Handler et al. 2015 8 ). Adherence to the three doses of the vaccine has also been low in Latin American countries, such as Brazil, Mexico, and Argentina (Tabakman 2017 24 ). This occurs after complaints of various symptoms, including suicides in Colombian girls after receiving the vaccine (Tabakman 2017 24 ).

Japan, after four years since its introduction, suspended the recommendation to immunize against HPV in 2014 (Larson et al. 2014 12 ). The decision was made after reported cases of chronic pain and other symptoms. Despite the reviews claiming that these reported cases were not related to the vaccine, no agreement was reached between Japan and the World Health Organization (WHO). Japan has previously shown to have very stringent thresholds for risk acceptance. One example of such, occurred during the bovine spongiform encephalopathy crisis, where, Japan re-examined meat samples imported from the US regardless of the safety assurance from the United States Department of Agriculture (USDA) and ultimately decided to suspend the importation of meat from the United States.

 

Adverse reactions to the HPV vaccine - According to HPV vaccine manufacturers, the most common adverse reactions to Gardasil include pain, swelling, redness, stinging, bruising, bleeding at the injection site, and headache, fever, nausea, diarrhea, abdominal pain, and syncope (https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM111263.pdf). For Cervarix, local adverse reactions occurring in ≥ 20% of subjects are pain, redness, and swelling at the site of injection. The most common general adverse events in ≥ 20% of the subjects are fatigue, headache, myalgia, gastrointestinal symptoms, and arthralgia (FDA).

The most frequent reported symptoms of HPV vaccination are chronic pain with paresthesia, headaches, fatigue, and orthostatic intolerance (Martínez-Lavin 2015 14 ). Small series and isolated cases of complex regional pain syndrome (CRPS), postural orthostatic tachycardia syndrome (POTS), and fibromyalgia, have been reported after vaccination against HPV. These conditions are often difficult to diagnose, and show similar clinical characteristics (Goldenberg 2009 7 ).

Apparently, dysfunction of the sympathetic nervous system plays an important role in the pathogenesis of these syndromes (Martínez-Lavin 2015 14 ). Ninety three percent of affected subjects continue to have disabling symptoms for more than four years, unable to return to school or work (Tomljenovic et al. 2014 25 , Martínez-Lavin et al. 2015 13 ). Other studies, nevertheless, have shown a lack of evidence of an association between HPV vaccine and CRPS (Weinbaum and Cano 2015 26 ) or fatigue (Donegan et al. 2013 4 , Feiring et al. 2017 5 ).

It should be mentioned that chronic arthropathy has also been observed with other vaccines, such as the rubella vaccine.

 

HPV vaccine safety - The recommendation for the use of HPV vaccine by the WHO is based on efficacy and effectiveness data (WHO 2017a 27 ). The Global Advisory Committee for the Safety of Vaccines (GACVS) is an independent body composed of clinicians and expert scientists, who meet under the WHO to provide rigorous advice on the safety of vaccines of global importance. In its latest report, the committee has evaluated the risk of developing Guillain-Barré syndrome, concluding that the risk is no more than 1 case per 1 million vaccinated (WHO 2017b 28 ). The committee has also found no evidence of causality between the HPV vaccine and SDRC or STPO, and considers that there is still no evidence suggestive of a causal association for the various symptoms (including pain and motor dysfunction) after reviewing data obtained from surveillance in Japan. A review of the HPV vaccine safety by the Centers for Disease Control and Prevention (CDC) found no difference in side effects between vaccinated and unvaccinated individuals (Gee et al. 2016 6 ). In fact the CDC’s Vaccine Adverse Event reporting System (VAERS) states that the HPV vaccine is very safe, and has not found any unexpected patterns in maternal or fetal outcomes (Moro et al. 2015 15 ).

These conclusions, however, are based on records that should be interpreted with care, especially when assessing cases with non-specific diagnosis, for which there is not a clear consensus on the diagnostic criteria (Goldenberg 2009 7 ) (Fig. 1).

Despite these pronouncements on the safety of HPV vaccine, regions in Colombia have reported a disproportionate number of neuropathic pain cases (with respect to the expected reactions declared by the pharmaceutical company producing Gardasil) (Sánchez-Gómez and Hernández-Flórez 2014 21 ).

It is important to note that the occurrence of demyelinating disease after vaccination, despite being low, is not negligible. This type of complication has been reported for multiple vaccines such as influenza, HPV, hepatitis A or B, rabies, measles, rubella, yellow fever, anthrax, meningococcus, and tetanus.

 

Post-vaccination syndromes: beyond adjuvants - The presence of viral nucleic acids can cause autoimmune phenomena (Jeffs et al. 2016 10 ). HPV vaccines, however, are composed of proteins as we previously described. An adjuvant is a substance commonly used in vaccines in order to increase the immune response against an antigen. The quadrivalent vaccine of Gardasil (Merck) contains a simple adjuvant of aluminum hydroxide (225 mg). The nonavalent vaccine contains twice the concentration of adjuvant (500 mg of Aluminum)(Gee et al. 2016 6 ). The Cervarix vaccine uses a proprietary adjuvant, 3-O-desacyl-4 monophosphoryl lipid A (AS04), which appears to be more potent (Handler et al. 2015 8 ).

The term “ASIA” (Autoimmune/inflammatory Syndrome Induced by Adjuvants) describes a spectrum of clinical conditions that share similar signs and symptoms, including somatoform and dysautonomic post-vaccination phenomena (Palmieri et al. 2017 18 ). With respect to the HPV vaccine, it has been estimated that the rate of ASIA syndrome is 3.6 cases per 100,000 doses of anti-HPV vaccine (95% CI 3.4-3.7). The most common clinical manifestations are pyrexia (58%), myalgia (27%) and arthralgia or arthritis (19%).

It would not be the first time that adjuvants in a vaccine cause an adverse reaction. The use of AS03 as an adjuvant in the Pandemix vaccine against the influenza virus was linked to the development of autoimmune narcolepsy.

A recent study, however, shows that aluminum present in the adjuvant does not play a role in cellular hypersensitivity (Poddighe et al. 2017 19 ). On the other hand, a review of the adverse effects in clinical trials comparing women who received the bivalent vaccine vs. those who received the aluminum placebo, showed an increase in deaths in the vaccinated group. This result cautions of a projected greater systemic adverse effects with the nonavalent vaccine. Furthermore, there is also a report of autoimmune thrombocytopenia with antiphospholipid antibodies after HPV vaccination (Bizjak et al. 2016 1 ).

Equally important, the absence of symptoms does not exclude the presence of an inflammatory phenomenon, with epipharingitis being found in all women examined after HPV vaccination in Japan (Hotta et al. 2017 9 ). This phenomenon is more severe if the patient has a predisposition to develop autoimmune diseases such as lupus (Soldevilla et al. 2012 23 ) (Fig. 2). Another reported post-HPV vaccination syndrome is called multiple evanescent white dot syndrome, a rare retinopathy of unknown origin (Ogino et al. 2014 17 ). The favorable response to immunosuppressive therapy suggests an autoimmune phenomenon, or at least an imbalance in immune function (Fig. 2).

This evidence justifies the call made in countries such as Colombia for the identification of predictive markers to develop autoimmune diseases in the population to be vaccinated against HPV.

 

In conclusion - Apart from cultural and religious barriers, the adverse effects to HPV vaccines must be re-evaluated, since the initial clinical trials of the first vaccines were tested in different populations than women in Latin America or Japan. The role of the host immunogenetic background in HPV infection and the recognition of HPV antigens (Cervantes 2011 3 ) are important, and have been studied for decades. The benefit of vaccines is undoubtedly to reduce the incidence of infectious diseases, and in the case of HPV, prevent the development of persistent infections leading to cervical cancer. Even so, the side effects must be closely monitored, and reported without bias, to ensure that the benefits outweigh the risks.

 

AUTHORS' CONTRIBUTION

 

JC conceptualised the topic; A-H D and JC wrote the paper.

REFERENCES
01. Bizjak M, Bruck O, Kanduc D, Praprotnik S, Shoenfeld Y. Vaccinations and secondary immune thrombocytopenia with antiphospholipid antibodies by human papillomavirus vaccine. Semin Hematol. 2016; 53(Suppl. 1): S48-50.
02. Cervantes J, Lema C, Hurtado L, Andrade R, Quiroga G, Garcia G, et al. Prevalence of human papillomavirus infection in rural villages of the Bolivian Amazon. Rev Inst Med Trop São Paulo. 2003; 45(3): 131-5.
03. Cervantes JL. Multiple human papillomavirus infection: don’t forget the genetic background. J Infect Dis. 2011; 204(11): 1816-7.
04. Donegan K, Beau-Lejdstrom R, King B, Seabroke S, Thomson A, Bryan P. Bivalent human papillomavirus vaccine and the risk of fatigue syndromes in girls in the UK. Vaccine. 2013; 31(43): 4961-7.
05. Feiring B, Laake I, Bakken IJ, Greve-Isdahl M, Wyller VB, Haberg SE, et al. HPV vaccination and risk of chronic fatigue syndrome/myalgic encephalomyelitis: a nationwide register-based study from Norway. Vaccine. 2017; 35(33): 4203-12.
06. Gee J, Weinbaum C, Sukumaran L, Markowitz LE. Quadrivalent HPV vaccine safety review and safety monitoring plans for nine-valent HPV vaccine in the United States. Hum Vaccin Immunother. 2016; 12(6): 1406-17.
07. Goldenberg DL. Diagnosis and differential diagnosis of fibromyalgia. Am J Med. 2009; 122(Suppl. 12): S14-21.
08. Handler NS, Handler MZ, Majewski S, Schwartz RA. Human papillomavirus vaccine trials and tribulations: vaccine efficacy. J Am Acad Dermatol. 2015; 73(5): 759-67.
09. Hotta O, Tanaka A, Torigoe A, Imai K, Ieiri N, Japanese Focal Inflammation Research Group. Involvement of chronic epipharyngitis in autoimmune (auto-inflammatory) syndrome induced by adjuvants (ASIA). Immunol Res. 2017; 65(1): 66-71.
10. Jeffs LS, Nitschke J, Tervaert JW, Peh CA, Hurtado PR. Viral RNA in the influenza vaccine may have contributed to the development of ANCA-associated vasculitis in a patient following immunisation. Clin Rheumatol. 2016; 35(4): 943-51.
11. Kirby T. FDA approves new upgraded Gardasil 9. Lancet Oncol. 2015; 16(2): e56.
12. Larson HJ, Wilson R, Hanley S, Parys A, Paterson P. Tracking the global spread of vaccine sentiments: the global response to Japan’s suspension of its HPV vaccine recommendation. Hum Vaccin Immunother. 2014; 10(9): 2543-50.
13. Martínez-Lavin M, Martínez-Martínez LA, Reyes-Loyola P. HPV vaccination syndrome. A questionnaire-based study. Clin Rheumatol. 2015; 34(11): 1981-3.
14. Martínez-Lavin M. Hypothesis: human papillomavirus vaccination syndrome - small fiber neuropathy and dysautonomia could be its underlying pathogenesis. Clin Rheumatol. 2015; 34(7): 1165-9.
15. Moro PL, Zheteyeva Y, Lewis P, Shi J, Yue X, Museru OI, et al. Safety of quadrivalent human papillomavirus vaccine (Gardasil) in pregnancy: adverse events among non-manufacturer reports in the Vaccine Adverse Event Reporting System 2006-2013. Vaccine. 2015; 33(4): 519-22.
16. Muñoz N, Reina JC, Sánchez GI. La vacuna contra el virus del papiloma humano: una gran arma para la prevención primaria del cáncer de cuello uterino. Colombia Med. 2008; 39(2): 196-2014.
17. Ogino K, Kishi S, Yoshimura N. Multiple evanescent white dot syndrome after human papillomavirus vaccination. Case Rep Ophthalmol. 2014; 5(1): 38-43.
18. Palmieri B, Poddighe D, Vadala M, Laurino C, Carnovale C, Clementi E. Severe somatoform and dysautonomic syndromes after HPV vaccination: case series and review of literature. Immunol Res. 2017; 65(1): 106-16.
19. Poddighe D, Vadala M, Laurino C, Palmieri B. Somatoform and neurocognitive syndromes after HPV immunization are not associated to cell-mediated hypersensitivity to aluminum. Toxicol In Vitro. 2017; 43: 58-61.
20. Remes O, Smith LM, Alvarado-Llano BE, Colley L, Levesque LE. Individual - and regional-level determinants of human papillomavirus (HPV) vaccine refusal: the Ontario Grade 8 HPV vaccine cohort study. BMC Public Health. 2014; 14: 1047.
21. Sánchez-Gómez FJ, Hernández-Flórez LJ. La vacunación contra el vírus del papiloma humano en Colombia. Revista Geren Polit Salud. 2014; 13(27): 05-9.
22. Skeate JG, Woodham AW, Einstein MH, da Silva DM, Kast WM. Current therapeutic vaccination and immunotherapy strategies for HPV-related diseases. Hum Vaccin Immunother. 2016; 12(6): 1418-29.
23. Soldevilla HF, Briones SF, Navarra SV. Systemic lupus erythematosus following HPV immunization or infection? Lupus. 2012; 21(2): 158-61.
24. Tabakman R. El fracaso de la aplicación de la vacuna contra el virus del papiloma humano en Latinoamérica. Medscape. 2017. Available from: http://www.fasgo.org.ar/images/Fracaso_HPV.pdf.
25. Tomljenovic L, Colafrancesco S, Perricone C, Shoenfeld Y. Postural orthostatic tachycardia with chronic fatigue after HPV vaccination as part of the “autoimmune/auto-inflammatory syndrome induced by adjuvants”: case report and literature review. J Investig Med High Impact Case Rep. 2014; 2(1): 2324709614527812.
26. Weinbaum CM, Cano M. HPV vaccination and complex regional pain syndrome: lack of evidence. EBioMedicine. 2015; 2(9): 1014-5.
27. WHO - World Health Organization. Human papillomavirus vaccines: WHO position paper, May 2017 - Recommendations. Vaccine. 2017a; 35(43): 5753-5.
28. WHO - World Health Organization. Safety update of HPV vaccines. 2017b. Available from: http://www.who.int/vaccine_safety/committee/ topics/hpv/June_2017/en/.

+ Corresponding author: jorge.cervantes@ttuhsc.edu
Received 2 February 2018
Accepted 8 May 2018

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