Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Vaccines for the twenty-first century society

A Corrigendum to this article was published on 30 January 2012

This article has been updated


Vaccines have been one of the major revolutions in the history of mankind and, during the twentieth century, they eliminated most of the childhood diseases that used to cause millions of deaths. In the twenty-first century, vaccines will also play a major part in safeguarding people's health. Supported by the innovations derived from new technologies, vaccines will address the new needs of a twenty-first century society characterized by increased life expectancy, emerging infections and poverty in low-income countries.


Health is probably the most important value of our society, which enjoys an unprecedented quality of life in high-income countries and improving conditions in poor countries. A lot of the progress made so far in improving healthcare has been due to the conquest of infectious diseases, an area in which vaccination has played a major part. During the past three decades, the vaccine field has been transformed by new technologies, and vaccination has the potential to have a very important role in the future as well. There is much excitement about the contributions that vaccines have made and will continue to make to our society this century, and several initiatives have been launched to better capture the full potential of what vaccines may deliver. The most important ones are the Decade of Vaccines launched by the Bill and Melinda Gates Foundation, the Millennium Development Goals of the United Nations, and the initiative of the US Institute of Medicine to identify and prioritize new preventive vaccines for development (Box 1). Here, we describe how vaccines may contribute to addressing the health needs of the twenty-first century, which is characterized by an aging society, emerging infections and poverty in low-income countries.

Vaccines for all ages

One of the great successes of modern society in high-income countries is the increase in life expectancy (Fig. 1). In countries with the longest life expectancy, average lifespan was 35 years in 1750 (Ref. 1) and 45 years in 1840, and this has since increased by approximately 2.5 years per decade, reaching 55 years in 1900 and 65 years in 1950 (Refs 2, 3). Today, life expectancy is above 80 years and, bearing in mind that predictions of a ceiling to life expectancy have been repeatedly wrong, we can extrapolate that it could reach 100 years in six decades2. A major reason for the steady increase of life expectancy is greater control of infectious diseases — this has led to decreased early mortality (only one in four children used to reach the age of 20) and has also provided a longer lifespan in adults by decreasing their exposure to acute and chronic inflammatory processes1.

Figure 1: Increase in life expectancy.
figure 1

The graph shows the increase in life expectancy that occurred in the countries with longest lifespans1,2,3 from 1750 to the present day and also the projected increase in longevity for this century. The average life expectancy for individuals in the society for which most vaccines were developed was 60–65 years. This society was characterized by a high proportion of children and young people, and is quite different from today's society, which is characterized by a high proportion of elderly people and a life expectancy of more than 80 years.

Vaccination served extremely well the needs of our twentieth-century society, members of which had a life expectancy of approximately 55–65 years. By eliminating many infectious diseases that used to cause millions of deaths, vaccination contributed to the increase in our lifespan (Fig. 1). Key contributions made by vaccination include the eradication of smallpox from our planet, the almost complete elimination of poliomyelitis, and a decrease of more than 95% in the incidence of diseases such as diphtheria, tetanus, pertussis, measles, mumps and rubella. More recently, vaccines against hepatitis A, hepatitis B, Haemophilus influenzae type b and pneumococcus have further decreased the mortality caused by infectious diseases4.

The key question for this article is whether vaccination will be able to significantly contribute to the health needs of the members of a twenty-first century society, who have a current lifespan of more than 80 years and a predicted future lifespan of 100 years. Today, developed countries have a low proportion of children and young adults, and a high proportion of elderly people (Fig. 1). This composition is quite different from the one for which most vaccines were developed, and today's society clearly has quite different medical needs. To answer the question of whether vaccines will be able to contribute to the needs of the twenty-first century society, we need to look at the health needs of this society and then ask whether we have the technologies to address these needs. Here, we describe each of the main stages of life and how the health needs of each age group in the twenty-first century could be addressed by vaccination (Fig. 2).

Figure 2: Target population for vaccines in the twenty-first century.
figure 2

a | The most important vaccines for each age group are reported. b | Special target groups for vaccination in the twenty-first century. The most important vaccines for each target group are reported. The lists of vaccines reported are indicative and they are not intended to be exhaustive. C. difficile, Clostridium difficile; E. coli, Escherichia coli; EV71, enterovirus 71; H. influenzae, Haemophilus influenzae; K. pneumoniae, Klebsiella pneumoniae; P. aeruginosa, Pseudomonas aeruginosa; S. aureus, Staphylococcus aureus; SARS, severe acute respiratory syndrome.

Pre-birth. In the past, pregnant women had high levels of antibodies against a range of pathogens to which they had been exposed, and they transferred protective immunity to their unborn fetus and then to their newborn baby via transplacental transfer of antibodies and by breast feeding. Today, young women are less exposed to infectious agents, and breast feeding is less common and of shorter duration. Therefore, mothers transfer fewer protective antibodies to their infants. The consequence is that newborns are not protected against various pathogens and diseases, including cytomegalovirus, influenza virus, group B streptococcus, hepatitis B virus, meningococcus (groups A, B, C, Y and W135), pertussis, respiratory syncytial virus and tetanus. With the exception of the hepatitis B virus vaccine and bacille Calmette–Guérin (BCG) that in some countries are given at birth, present immunization schedules start mostly at two months of age5,6. Consequently, the present immunization schedules do not induce protection against the majority of these diseases until the fifth month of life or later. This leaves a period of vulnerability during the first 4–6 months of life, which is associated with significant mortality and morbidity. A recent increase in the frequency of pertussis cases and subsequent mortality in infants younger than 5 months is an example of this trend7.

Recent successes involving the vaccination of pregnant women against neonatal tetanus8 and influenza virus9 in order to promote immunity in neonates have shown that vaccination before birth is safe and very effective in providing newborns and their mothers with protection from these pathogens. These studies show that vaccination can promote the natural immune protection in newborns that human evolution has selected for but which has been weakened as a result of decreased exposure of mothers to infectious agents. As most of the vaccines discussed above are already available and vaccines against meningococcus, respiratory syncytial virus and group B streptococcus are in development, we believe that children of the twenty-first century can be well-protected in the first months of life by vaccinating their mothers.

Infants and children. This age group is the one that is best-served by the present vaccination schedule. Currently, it is recommended that children are immunized against diphtheria, tetanus, pertussis, hepatitis B virus, H. influenzae type b, poliovirus, Streptococcus pneumoniae, rotavirus, measles, mumps and rubella5,6 (Fig. 2a). This immunization schedule should remain in place, and further immunizations against meningococcus, respiratory syncytial virus, influenza virus, group A streptococcus and Helicobacter pylori can be added to the schedule when these vaccines become available. Vaccination against hepatitis A virus can also be added to the schedule.

Importantly, once a proper programme of maternal immunization is implemented, it will be possible to relax the aggressive immunization schedules of today, in which children receive immunizations at 2, 3, 4 and 12 months of age or at 2, 4, 6 and 12 months of age5,6. Although these schedules are designed to induce protective immunity early in life, they are not optimal for effective priming of the still-immature immune system. Better priming, and different regimes, such as immunization at 3 and 5 months with a booster at 12 months may be considered. We need, however, to ensure that maternal immunization does not interfere with infant vaccination, since it is well known that the presence of maternal antibodies can prevent the infants from mounting optimal immune responses against live-attenuated viral vaccines, such as that used for measles, by interfering with viral replication. These effects are usually not present, even if in some cases they have been reported for inactivated vaccines, such as whole-cell pertussis, and therefore their presence needs to be assessed for each new vaccine10.

Adolescents. In some countries, vaccination against human papilloma virus and meningococcus serogroups A, C, Y and W135 is already recommended for adolescents. In addition, adolescents could receive a booster vaccine against diphtheria, tetanus and pertussis, and booster vaccines against influenza virus and meningococcus group B when these become available. Immunization against Epstein–Barr virus, herpes simplex virus, cytomegalovirus and parvovirus B19 will also be desirable when these vaccines become available.

Adults. Currently, adults in some countries receive scheduled vaccinations against tetanus and influenza. However, many times they are only vaccinated in special circumstances, such as when working with potentially infected human samples or when travelling to disease-affected areas (discussed in more detail below). However, an immunization schedule should be established for adults and should include vaccination against emerging strains of influenza virus and periodic boosts to maintain immunity to diphtheria, tetanus, pertussis, hepatitis B virus, respiratory syncytial virus and meningococcus (groups A, B, C, Y and W135).

Elderly individuals. An important target group for the development of new vaccines will be the elderly, a demographic group for which vaccines have not been fully exploited yet. This population has several new medical needs. First, the aging immune system makes them more vulnerable to many infections against which they were previously immune. Susceptibility to infections, such as influenza virus, meningococcus, group B streptococcus, pneumococcus, respiratory syncytial virus and varicella zoster virus, becomes higher in this age group; as such, they will need more-frequent booster vaccinations, in many cases with vaccines potentiated by adjuvants that are specifically designed to stimulate the aging immune system to respond better to vaccination. One example of a licensed adjuvant that has been efficiently used to boost immune responses in the elderly is the oil-in-water emulsion MF59 (Novartis), which is licensed for use as an adjuvanted seasonal influenza vaccine in European countries and in several other countries and has been shown to reduce hospitalization in the elderly11. Other licensed or experimental adjuvants are good candidates for novel vaccines for elderly patients in the future (Table 1).

Table 1 Vaccine adjuvants

The second medical need for the elderly is immunity to antibiotic-resistant bacteria that are acquired during hospitalization — these infections are most frequent in this age group. Therefore, it would be useful to vaccinate the elderly against Staphylococcus aureus, Clostridium difficile, Candida spp., Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae and Acinetobacter baumannii.

Another important medical need for this population is a strategy for the prevention of cancer. The risk of most cancers increases with age and the question is whether we can prevent or delay the age at which cancers strike. Tumours caused by infectious agents, such as certain liver12, cervical13 and stomach14 cancers, can be eliminated by preventing infection through vaccination. In addition, some cancers that are not associated with infectious agents, such as breast, colorectal and prostate cancer, could be prevented by vaccination with self antigens that are preferentially expressed by the tumour cells. Antigens such as lactalbumin and human epidermal growth factor receptor 2 (HER2; also known as neu and ERBB2) have been shown to work as vaccination targets in animal models of breast cancer. In addition, vaccines targeting mucin 1 (MUC1) have shown promise against colorectal cancer in early trials, and several antigens are being evaluated against prostate cancer15. These vaccines would induce protective immunity before tumour formation and should be able to provide early protection against emerging tumours. This will require the identification of antigens that can provide protection without inducing undesired autoimmune phenomena.

Vaccines for other groups

In addition to the vaccines required for different age groups, there are a number of other groups of people with distinct needs who will require special considerations (Fig. 2b).

Travellers. Travellers of all ages should be vaccinated against the diseases that they may find in the areas they travel to. Vaccines against the following pathogens and diseases can be considered before travelling: cholera, dengue, enterotoxigenic E. coli (ETEC), influenza virus, hepatitis A virus, hepatitis B virus, Japanese encephalitis virus, malaria, meningococcus (groups A, B, C, Y, W and X), paratyphoid fever, rabies, Shigella spp., tick-borne encephalitis virus, tuberculosis, typhoid fever and yellow fever. Although vaccines exist for several of these diseases, there is a significant need for effective vaccines against dengue, cholera, ETEC, malaria, Shigella spp. and paratyphoid fever. In addition, travellers would benefit from safer vaccines against yellow fever and more-effective vaccines against typhoid fever.

Patients with chronic diseases. People with chronic diseases, such as autoimmune disease and immunosuppressive disorders, and individuals with chronic respiratory or cardiac disease have special vaccination needs that are specific to their condition. Some vaccines that should be considered include those against cytomegalovirus, influenza virus, fungal infections (such as those caused by Aspergillus spp. and Candida spp.), parainfluenza, P. aeruginosa, respiratory syncytial virus, S. aureus and tuberculosis. Patients with hereditary haemoglobinopathies, such as sickle-cell anaemia, should be protected against infection with parvovirus B19.

Patients with HIV. Patients with HIV may also consider vaccination against influenza virus, pneumococcus, pneumocystosis and tuberculosis. However, as these subjects are immunocompromised, many live-attenuated vaccines may be dangerous or not well tolerated. Therefore, subunit vaccines, possibly supported by potent adjuvants, may be required to elicit protective responses.

Emerging infections

More than 30 emerging or re-emerging infections have been identified during the past 30 years16,17 (Table 2). Among these are previously unrecognized diseases, such as AIDS, severe acute respiratory syndrome (SARS), avian and swine influenza and enterovirus 71 (EV71), and re-emerging diseases, such as anthrax, cholera, dengue, diphtheria, Ebola virus disease, malaria, tuberculosis, West Nile virus infection, meningococcus X and plague (Fig. 2b). In addition, several infectious diseases that cause significant morbidity and mortality, such as malaria and HIV, have resisted attempts to develop effective vaccines. The growth of the human population, global travelling and the changes in our planet's ecosystems suggest that novel infectious diseases will continue to emerge. In many cases, it will be possible to control these emerging threats by vaccination; however, this will require a coordinated effort involving the public and private sectors and the regulatory agencies to ensure that the appropriate technologies, manufacturing capacity and financial resources will be available when needed. Examples in which the public and private sector have been combining resources to fight emerging infections include the PATH Malaria Vaccine Initiative (MVI), the Global HIV Vaccine Enterprise, the tuberculosis initiative Aeras, and the preparation for pandemic influenza.

Table 2 Examples of newly emerging and re-emerging infectious diseases*

The MVI is a PATH initiative to develop a malaria vaccine. The most advanced programme is the one in collaboration with GlaxoSmithKline, in which the sporozoite antigen RTS,S adjuvanted with AS01, a combination of liposomes, a saponin called QS21 and monophosphoryl lipid A (MPL) (Table 1), showed 30–50% efficacy in Phase II studies and a 55.8% efficacy against clinical disease in Phase III clinical trials in Africa18. The Global HIV Vaccine Enterprise is a global alliance involving most of the stakeholders in HIV vaccine development. The alliance is developing a new strategic vision for the development of an HIV vaccine19. The goal is to assure the efficient development of an effective vaccine through the collaboration of all players. Aeras is a non-profit initiative dedicated to the development of novel tuberculosis vaccines. The organization is planning to perform several clinical trials to test the efficacy of new vaccines in the near future20. In the case of avian influenza, the public sector has been sponsoring clinical trials and the development of novel technologies for vaccine manufacturing, such as the production of influenza vaccines in cell culture21. Such technological advances, if applied to seasonal influenza vaccinations, could provide influenza vaccines that are more rapidly available and safer.

In most cases, emerging infections require the fast development of new vaccines, and novel adjuvants have a key role in this. A great example has been the recent pandemic influenza caused by the H1N1 virus. In this instance, the availability of licensed oil-in-water emulsion adjuvants, such as MF59 and AS03 (GlaxoSmithKline) (see Table 1 on licensed adjuvants), allowed the production of more doses of vaccine, by reducing the quantity of antigen needed in each vaccine dose, and resulted in an effective vaccine for all age groups. An additional benefit of adjuvants is the possibility to anticipate pandemics. For instance, today we have the possibility to prevent the risk of avian influenza by priming the population with an adjuvanted vaccine containing an H5N1 strain22,23 or by vaccinating against H2N2, an old virus for which humans no longer have any immunity. This virus still circulates in birds and pigs, from which it could cross the species barrier and be newly introduced into humans, as has happened for H1N1 in 2009 (Ref. 24). However, overall, even expanded cell culture production capacities and the use of adjuvants would not suffice to produce vaccine for the entire world population of approximately seven billion people in a timely manner in the case of a new and rapidly spreading pandemic disease agent. Therefore, the continued research into novel technologies, such as recombinant, vectored, nucleic-based and synthetic vaccines, remains a priority.


Infectious diseases can be a major cause of poverty. A study published in Science in 2008 (Ref. 25) found that, in sub-Saharan Africa, when a case of meningococcal meningitis strikes a family, the entire family income of several years can be spent to take care of the sick family member. This causes a spiral of poverty from which the family will never recover. Conversely, in cases in which families remained free from infectious diseases, they could build their own sustainable economic basis. In his recent speech addressing the world health assembly, Bill Gates said that “healthy people can drive thriving economies” (Ref. 26). Vaccines are by far the most effective tools to quickly eliminate infectious diseases in low-income countries and provide them the opportunity to fight poverty. There are many examples, such as the meningococcus C vaccination campaign in the United Kingdom27 and the recent vaccination against meningococcus A in Africa28, in which successful vaccination campaigns have eliminated diseases in entire countries within one year. A number of vaccines are needed to help fight poverty in low-income countries (Fig. 2b). Some of these vaccines are already available, or soon will be, in high-income countries, including vaccines against hepatitis A virus, hepatitis B virus, influenza virus, meningococcus (serogroups A, B, C, Y and W135), rabies, rotavirus and yellow fever virus. Other vaccines that may not be necessary for high-income societies but that are urgently needed in low-income countries, include vaccines against cholera, dengue, ETEC, Japanese encephalitis virus, hepatitis E, malaria, meningococcus X, parasitic infections, Salmonella typhi, Salmonella paratyphi, Salmonella typhimurium, Salmonella enterica, Shigella spp. and tuberculosis.

Today, there are two main obstacles to the development of vaccines for low-income countries. First, our society has no mechanism to develop those vaccines that are only needed in low-income countries and for which there is no market in high-income countries. Second, those vaccines for which there is also a medical need in high-income countries are optimized mostly for the medical needs of these countries, and they are suboptimal for the medical needs of low-income countries. For instance, polio and rotavirus vaccines are less effective in the developing world. Furthermore, these vaccines only became available in low-income countries 10–20 years after their introduction in high-income countries.

Recently, and for the first time, some initiatives have been launched to effectively address these problems. Examples of organizations and projects that aim to develop vaccines specifically for low-income countries are the International Vaccine Institute in Korea, the Novartis Vaccines Institute for Global Health, the Sabin Vaccine Institute, the Hilleman Laboratories, and the Meningitis Vaccine Project. Their missions and activities are described in Box 2. Progress has also been made in developing mechanisms to accelerate the availability of existing vaccines to low-income countries. The most innovative mechanism is the pneumococcal Advanced Market Commitment (AMC) of the GAVI alliance, an initiative in which five countries (Canada, Italy, Norway, Russia and the United Kingdom) and the Bill and Melinda Gates Foundation committed US$1.5 billion to purchase the newly developed pneumococcus vaccine and make it available to those countries that cannot afford it. Although these initiatives show that we are making progress in the field, a much stronger coordination between public sector, private sector, regulatory bodies and funding agencies will be necessary to make an impact in the short term and capture the unique opportunity to provide good health for every human being.

New vaccine development technologies

Will we be able to develop vaccines against many of the new challenging medical needs of our society? Clearly, vaccines to prevent tumours are still at an early stage in their development, and we are struggling to develop effective vaccines against several infectious agents, including HIV, tuberculosis and malaria. However, thanks to the revolutionary technologies of the past 20 years, vaccines have become much safer and it is now possible to develop vaccines against infectious agents or diseases that could not be effectively targeted using early vaccination methods (Fig. 3). For example, recombinant DNA technology made possible the development and large-scale manufacture of the hepatitis B vaccine; conjugation technology made possible the development of vaccines against H. influenzae type b, pneumococcus and meningococcus; genomics has allowed the discovery of new antigens by reverse vaccinology and made possible the development of a vaccine against meningococcus B. Following this example, the genome approach provided promising antigen targets for vaccines against group B streptococcus, group A streptococcus and pneumococcus, as well as for antibiotic-resistant bacteria, such as S. aureus. Novel technologies, such as the virus-like particles that allowed the development of a vaccine against papilloma virus, nucleic acid vaccines and synthetic vaccines are promising to start a revolution in the vaccine field. Furthermore, scientists have made great progress in understanding the human immune system and in developing novel adjuvants. For more than 70 years, aluminium salts have been the only adjuvants licensed for human use worldwide. In the past decades, oil-in-water emulsions and liposome-based adjuvants have been licensed in Europe. AS04 (GlaxoSmithKline), an adjuvant composed of aluminium salt and the Toll-like receptor (TLR) agonist MPL, has been licensed for use in a vaccine against human papilloma virus (Table 1). In addition, several novel adjuvants targeting other TLRs, such as TLR9, TLR7 and TLR2, are in the advanced developmental stage29 (Table 1), either alone or in combination with different classes of adjuvants, such as alum, emulsions, saponins and liposomes.

Figure 3: Technologies for vaccine development.
figure 3

Since the times of Pasteur, vaccines have been developed using empirical approaches consisting mostly of killed or live-attenuated microorganisms, partially purified components of pathogens (subunit vaccines), detoxified toxins or polysaccharides. These vaccines have been very successful in eliminating many devastating diseases. During the past 30 years, subsequent waves of new technologies have made possible vaccines that were impossible with the empirical approaches. These include recombinant DNA technology, glycoconjugation, reverse vaccinology and many emerging next-generation technologies, such as novel adjuvants, synthetic biology and structure-based vaccine design (structural vaccinology), that promise a very successful future for vaccines. BCG, bacille Calmette–Guérin; C. difficile, Clostridium difficile; E. coli, Escherichia coli; H. influenzae, Haemophilus influenzae; MMRV, measles, mumps, rubella, varicella; S. aureus, Staphylococcus aureus.

The fast development of new technologies (Table 3), suggests that we will soon be able to develop effective vaccines against many new pathogens, improve the safety and efficacy of the existing vaccines, and start to tackle novel targets for the treatment of diseases such as chronic infectious diseases and cancer.

Table 3 New and improved technologies and resulting vaccines


We believe that vaccines will be as important to our society in the twenty-first century as they were in the twentieth century, if not even more so. They will serve every age group and will become the most efficient 'life insurance' of the twenty-first century, contributing to a disease-free life of longer duration and better quality for many members of modern society. In addition, we believe that, in the medium term, the progress scientists are making in understanding the immune system will enable the development of therapeutic vaccines to fight pre-existing diseases, such as those resulting from chronic infections and cancer.

Change history

  • 30 January 2012

    On page 872 of the original version of this article, under the subheading "New vaccine development technologies", there was an error in the sentence that began: "AS04 (GlaxoSmithKline), an adjuvant composed of aluminium salt and the Toll-like receptor (TLR) against MPL". This sentence should begin: "AS04 (GlaxoSmithKline), an adjuvant composed of aluminium salt and the Toll-like receptor (TLR) agonist MPL". The authors apologize for this error.


  1. Crimmins, E. M. & Finch, C. E. Infection, inflammation, height, and longevity. Proc. Natl Acad. Sci. USA 103, 498–503 (2006).

    CAS  Article  Google Scholar 

  2. Oeppen, J. & Vaupel, J. W. Demography. Broken limits to life expectancy. Science 296, 1029–1031 (2002).

    CAS  Article  Google Scholar 

  3. Kirkwood, T. B. A systematic look at an old problem. Nature 451, 644–647 (2008).

    CAS  Article  Google Scholar 

  4. Rappuoli, R., Miller, H. I. & Falkow, S. The intangible value of vaccination. Science 297, 937–939 (2002).

    CAS  Article  Google Scholar 

  5. Centers for Disease Control and Prevention. Recommended immunization schedules for persons aged 0–18 years — United States. Morb. Mortal. Wkly Rep. 60 (5), 1–4 (2011).

  6. Immunization, Vaccines and Biologicals, World Health Organization [online], (2011).

  7. Centers for Disease Control and Prevention. Notes from the Field: Pertussis --- California, January--June 2010. Morb. Mortal. Wkly Rep. 59, 817 (2010).

  8. Roper, M. H., Vandelaer, J. H. & Gasse, F. L. Maternal and neonatal tetanus. Lancet 370, 1947–1959 (2007).

    Article  Google Scholar 

  9. Zaman, K. et al. Effectiveness of maternal influenza immunization in mothers and infants. N. Engl. J. Med. 359, 1555–1564 (2008).

    CAS  Article  Google Scholar 

  10. Siegrist, C. A. The challenges of vaccine responses in early life: selected examples. J. Comp. Pathol. 137 (Suppl. 1), S4–S9 (2007).

    CAS  Article  Google Scholar 

  11. O'Hagan, D. T., Rappuoli, R., De Gregorio, E., Tsai, T. & Del Giudice, G. MF59 adjuvant: the best insurance against influenza strain diversity. Expert Rev. Vaccines 10, 447–462 (2011).

    CAS  Article  Google Scholar 

  12. Pineau, P. & Tiollais, P. Hepatitis B vaccination: a major player in the control of primary liver cancer. Pathol. Biol. (Paris) 58, 444–453 (2010).

    CAS  Article  Google Scholar 

  13. Romanowski, B. Long term protection against cervical infection with the human papillomavirus: review of currently available vaccines. Hum. Vaccin. 7, 161–169 (2011).

    Article  Google Scholar 

  14. Rupnow, M. F., Chang, A. H., Shachter, R. D., Owens, D. K. & Parsonnet, J. Cost-effectiveness of a potential prophylactic Helicobacter pylori vaccine in the United States. J. Infect. Dis. 200, 1311–1317 (2009).

    Article  Google Scholar 

  15. Eisenstein, M. Vaccines: know your enemy. Nature 471, S8–S9 (2011).

    CAS  Article  Google Scholar 

  16. Morens, D. M., Folkers, G. K. & Fauci, A. S. The challenge of emerging and re-emerging infectious diseases. Nature 430, 242–249 (2004).

    CAS  Article  Google Scholar 

  17. Morens, D. M., Folkers, G. K. & Fauci, A. S. Emerging infections: a perpetual challenge. Lancet Infect. Dis. 8, 710–719 (2008).

    Article  Google Scholar 

  18. The RTS,S Clinical Trials Partnership. First results of phase 3 trial of RTS,S/AS01 malaria vaccine in African children. N. Engl. J. Med. 18 Oct 2011 (doi:10.1056/NEJMoa1102287).

  19. Council of the Global HIV Vaccine Enterprise et al. The 2010 scientific strategic plan of the Global HIV Vaccine Enterprise. Nature Med. 16, 981–989 (2010).

  20. Kaufmann, S. Is the development of a new tuberculosis vaccine possible? Nature Med. 6, 955–960 (2000).

    CAS  Article  Google Scholar 

  21. HHS pandemic influenza implementation plan. Chapter 5: vaccines. United States Department of Human & Health Services [online] (2006).

  22. Galli, G. et al. Fast rise of broadly cross-reactive antibodies after boosting long-lived human memory B cells primed by an MF59 adjuvanted prepandemic vaccine. Proc. Natl Acad. Sci. USA 106, 7962–7967 (2009).

    CAS  Article  Google Scholar 

  23. Fragapane, E. et al. A heterologous MF59-adjuvanted H5N1 prepandemic influenza booster vaccine induces a robust, cross-reactive immune response in adults and the elderly. Clin. Vaccine Immunol. 17, 1817–1819 (2010).

    CAS  Article  Google Scholar 

  24. Nabel, G. J., Wei, C. J. & Ledgerwood, J. E. Vaccinate for the next H2N2 pandemic now. Nature 471, 157–158 (2011).

    CAS  Article  Google Scholar 

  25. Roberts, L. Infectious disease. An ill wind, bringing meningitis. Science 320, 1710–1715 (2008).

    CAS  Article  Google Scholar 

  26. Mr Bill Gates, Co-chair of the Bill & Melinda Gates Foundation. World Health Organization [online] (2011).

  27. Campbell, H., Borrow, R., Salisbury, D. & Miller, E. Meningococcal C conjugate vaccine: the experience in England and Wales. Vaccine 27, B20–B29 (2009).

    Article  Google Scholar 

  28. Sow, S. O. et al. Immunogenicity and safety of a meningococcal A conjugate vaccine in Africans. N. Engl. J. Med. 364, 2293–2304 (2011).

    CAS  Article  Google Scholar 

  29. Steinhagen, F., Kinjo, T., Bode, C. & Klinman D. M. TLR-based immune adjuvants. Vaccine 29, 3341–3355 (2011).

    CAS  Article  Google Scholar 

  30. Global health leaders launch decade of vaccines collaboration. Bill & Melinda Gates Foundation [online] (2010).

  31. Millennium Development Goals. United Nations Development Programme [online].

  32. Identifying and prioritizing new preventive vaccines for development. The National Acaedamies Current Projects System [online] (2010).

  33. Human hookworm vaccine initiative (HHVI). Sabin Vaccine Institute [online].

  34. Timeline. Meningitis Vaccine Project [online].

Download references


The authors are grateful to C. Mallia for editorial assistance and to G. Corsi for assistance with the artwork.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Rino Rappuoli.

Ethics declarations

Competing interests

The authors are employed by or have a consultancy contract with Novartis Vaccines.

Related links

Related links



GAVI Alliance

Global HIV Vaccine Enterprise

Hilleman Laboratories

International Vaccine Institute

Meningitis Vaccine Project

Novartis Vaccines

Novartis Vaccines Institute for Global Health


PATH Malaria Vaccine Initiative

Sabin Vaccine Institute

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Rappuoli, R., Mandl, C., Black, S. et al. Vaccines for the twenty-first century society. Nat Rev Immunol 11, 865–872 (2011).

Download citation

  • Published:

  • Issue Date:

  • DOI:

Further reading


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing