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Modelling the global burden of drug-resistant tuberculosis avertable by a post-exposure vaccine


There have been notable advances in the development of vaccines against active tuberculosis (TB) disease for adults and adolescents. Using mathematical models, we seek to estimate the potential impact of a post-exposure TB vaccine, having 50% efficacy in reducing active disease, on global rifampicin-resistant (RR-) TB burden. In 30 countries that together accounted for 90% of global RR-TB incidence in 2018, a future TB vaccine could avert 10% (95% credible interval: 9.7–11%) of RR-TB cases and 7.3% (6.6–8.1%) of deaths over 2020–2035, with India, China, Indonesia, Pakistan, and the Russian Federation having the greatest contribution. This impact would increase to 14% (12–16%) and 31% (29–33%) respectively, when combined with improvements in RR-TB diagnosis and treatment relative to a scenario of no vaccine and no such improvements. A future TB vaccine could have important implications for the global control of RR-TB, especially if implemented alongside enhancements in management of drug resistance.


The emergence of drug resistance poses a pressing challenge in the control of tuberculosis (TB) worldwide1. In 2018, an estimated 500,000 incident TB cases worldwide (out of a total of 10 million incident cases) were resistant to rifampicin, one of the key drugs in first-line anti-TB treatment2. Second-line treatment for these cases is costly, protracted and toxic, with an average treatment success of only 56%, compared to 85% for drug-sensitive TB2. Recent years have seen important advances in the development of shorter and safer regimens for treatment of rifampicin-resistant (RR-) TB3,4,5, as well as the potential for regimens to avoid using ineffective drugs by early detection of broader resistance profiles6,7; nonetheless, global uptake of these new regimens remains slow3.

Prevention of drug-resistant TB may be as important as improving patient outcomes for achieving desired reductions in the burden of disease8. Although recent years have seen notable advances in the development of simplified preventive regimens against drug-sensitive TB9,10, preventive therapy against drug-resistant infection is complicated by the fact that there is currently no assay for latent TB infection (LTBI) that can determine drug susceptibility of the infecting strain. In recent contacts of multidrug-resistant TB, preventive treatment can be tailored to the drug sensitivity status of the index case, but this approach does not address those with immunity to TB-specific antigens and no known contact. However, recent developments have raised the prospect of prevention through vaccination11. Informed in part by seminal modelling analysis12, in 2018 the World Health Organization (WHO) defined a preferred product profile for TB vaccine13. Amongst priorities for vaccine development, this document identified the ability to protect adults and adolescents with LTBI from developing the active form of the disease, with at least 50% efficacy, and offering at least ten years of protection13. In subsequent results from a phase 2b trial, amongst adults and adolescents with LTBI in Kenya and South Africa, the M72/AS01E (hereafter M72) vaccine decreased TB incidence by almost half14.

By offering protection regardless of drug sensitivity status, future TB vaccines may offer an important opportunity to reduce the transmission of drug-resistant TB, as well as the overall burden of TB. Prevention of TB through vaccination may have the corollary benefit of reducing population-level selection of resistant strains, as the use of anti-TB drugs declines. However, the potential impact of a future TB vaccine on the global burden of drug-resistant TB remains unknown. It is also uncertain how the impact of such a vaccine may compare with the uptake of new second-line regimens, that are shorter, safer and potentially more effective than earlier regimens involving injectable drugs5.

In the present work, we seek to address these questions using mathematical modelling of TB transmission dynamics, in 30 countries with a high burden of drug-resistant TB (Table 1). We modelled the potential impact of a rollout of an M72-like, ‘post-exposure’ vaccine (i.e. one intended for use amongst those already infected with TB) amongst adults and adolescents, and assessed health impacts between 2020 and 2035, with a focus on RR-TB. As a secondary analysis, we examined the potential contribution of a TB vaccine, to antimicrobial resistance more broadly than TB. There is evidence indicating that TB cases are often treated with empiric antibiotic therapy in primary care settings15, including the use of quinolones16,17. Therefore, if a vaccine reduces overall TB burden, it may also reduce the prevalence of symptoms that would trigger antibiotic consumption, reducing selection for resistance not only in TB but other pathogens or commensal bacteria that might be exposed18. We estimated the potential impact of a future TB vaccine, on reducing antibiotic consumption in this way.

Table 1 List of the 30 countries selected for the modelling analysis.



Supplementary Figs. 16 and Supplementary Table 1 show the results of model calibration in the 30 countries accounting for 90% of RR-TB incidence in 2018, based on four different model structures that capture variations in the epidemiology of TB and health systems across these countries (Table 1). Additional results show model validation with data that was not used for calibration, including prevalence surveys where available (Supplementary Fig. 7) and model-based estimates for the proportion of incident, drug-resistant TB that arises through transmission, rather than through treatment (Supplementary Fig. 8). Figure 1 shows illustrative results for RR-TB incidence trajectories in India, the Russian Federation, China, and Nigeria, as example countries representing each of the model structures (Table 1); Supplementary Fig. 9 shows these same dynamics, but illustrating the cases averted over time.

Fig. 1: Illustration of the projected impact on RR-TB of an M72-like vaccine.
figure 1

n = 200 posterior samples. Median (solid and dashed lines) and 95% Bayesian credible intervals (CrIs) of rifampicin-resistant tuberculosis (RR-TB) incidence rates over 2019–2035 are presented. For clarity, uncertainty regions with CrIs are only shown for the vaccine (not comparator) scenarios. These projections correspond to a post-exposure vaccine that reduces the risk of reactivation of latent TB infection by 50%, and that is implemented through routine vaccination and catch-up campaign amongst those over 15-years old. The figure shows projections for the countries with the highest absolute burden of RR-TB from each of the country categories listed in Table 1. Blue dashed curves illustrate a ‘status quo’ baseline, assuming no vaccine implementation and no change in the management of RR-TB. Blue solid curves show the impact of vaccination. Red curves show corresponding dynamics, under an alternative ‘improved RR-TB management’ baseline where the detection of RR-TB at the point of TB diagnosis is increased to 85%, and second-line treatment success is increased to 75%, in countries that have not yet achieved these targets. The Russian Federation in particular shows a lower impact of improved RR-TB management than other countries, owing to its already-higher coverage of drug susceptibility tests (Supplementary Fig. 10). Although the 95% CrIs for these projected dynamics with vaccination overlap in these regions, the overall incidence reductions are significant, in the sense of having uncertainty intervals that are strictly positive (Table 2, Supplementary Fig. 9).

Vaccine impact on RR-TB incidence

Figure 2 summarises the overall impact in terms of cumulative RR-TB cases averted between 2020 and 2035, illustrating dominant contributions from India and China, as well as from high-burden countries including Indonesia, Pakistan, the Russian Federation and Nigeria. Globally, relative to a status quo comparator, an M72-like vaccine would avert 620,000 cases (95% credible intervals [CrI]: 516,000–867,000) of RR-TB between 2020 and 2035 (Table 2). Molecular diagnostic tools are offering new opportunities for early recognition of rifampicin resistance19, while new, shorter, safer second-line regimens may facilitate improved treatment outcomes5. If use of an M72-like vaccine is combined with increased uptake of these tools (i.e. improved management of RR-TB), the overall impact would increase to 831,000 RR-TB cases (95% CrI: 643,000–1,170,000) averted.

Fig. 2: Country-wise contribution to vaccine-avertable incidence of RR-TB.
figure 2

The area of each square is proportional to the median estimate from n = 200 posterior samples, for the absolute number of avertable rifampicin-resistant tuberculosis (RR-TB) cases by a post-exposure, M72-like vaccine, between 2020 and 2035. Panel a shows cases averted by a vaccine alone, while panel b shows cases averted by a combination of a vaccine and measures to improve the management of RR-TB (both relative to a scenario of no vaccine, and no improvement in RR-TB, i.e. status quo). Countries are denoted by their ISO alpha-3 codes and their corresponding full names are listed in Table 1. Colours for each country are only for the purpose of display, and do not designate any quantitative scale.

Table 2 Summary of model-projected impact of a post-exposure, M72-like vaccine on RR-TB burden.

Figure 3 shows percent reductions of RR-TB cases by country. Globally, the effect of vaccination would be to avert 10% (95% CrI: 9.7–11%) of RR-TB cases between 2020 and 2035, relative to a status quo comparator (Table 2). Combined with improved RR-TB management, this impact would increase to 14% (95% CrI: 12–16%) of RR-TB cases. For countries having only small improvement gaps in coverage of drug susceptibility testing and success of second-line treatment, like Myanmar and Kazakhstan (Supplementary Fig. 10), improved management of RR-TB would have only limited incremental impact on RR-TB burden, in addition to vaccination. Supplementary Fig. 11 illustrates that, at the global level, ~2500 adolescents and adults with LTBI would need to be vaccinated to avert 1 RR-TB case.

Fig. 3: Projected percent cases of RR-TB averted by an M72-like vaccine.
figure 3

Rectangular bars show median estimates and error bars show 95% Bayesian credible intervals (CrIs), both estimated from n = 200 posterior samples for each country. Blue bars show the vaccine-avertable proportions of rifampicin-resistant tuberculosis (RR-TB) cases relative to a ‘status quo’ scenario, while adjacent bars together show averted proportions in combination with ‘improved RR-TB management’, as outlined in the caption to Fig. 1. The latter bars are stratified to show: (i) the impact of improved management of RR-TB alone, i.e. in the absence of vaccination (orange segment), and (ii) the incremental impact of vaccination, acting in combination with these improvements (red segment). Error bars on the stacked orange and red bars show the 95% CrIs of the total impact of a vaccine combined with improved management of RR-TB. Countries are ranked in a descending order according to the number of RR-TB incident cases in 2018.

Vaccine impact on RR-TB mortality

Figures 4 and 5 show corresponding results in terms of RR-TB mortality: globally, vaccination would avert 119,000 (95% CrI: 96,000–174,000) RR-TB deaths between 2020 and 2035, amounting to a reduction of 7.3% (95% CrI: 6.6–8.1%). Improvement in RR-TB management showed a greater impact on preventing mortality than incidence of RR-TB burden. When combined with vaccination, 499,000 (95% CrI: 391,000–729,000) RR-TB deaths would be averted between 2020 and 2035, amounting to a reduction of 31% (95% CrI: 29–33%) (Table 2). Supplementary Fig. 11 illustrates that, at the global level, ~13,000 adolescents and adults with LTBI would need to be vaccinated to avert 1 death from RR-TB. This estimate may vary by local settings, depending on country-specific rates of TB mortality.

Fig. 4: Country-wise contribution to vaccine-avertable deaths from RR-TB.
figure 4

As for Fig. 2, the area of each square here is proportional to the median estimate from n = 200 posterior samples, for the absolute number of avertable rifampicin-resistant tuberculosis (RR-TB) deaths by a post-exposure, M72-like vaccine, between 2020 and 2035. Panel a shows deaths averted by a vaccine alone, while panel b shows deaths averted by a combination of a vaccine and measures to improve the management of RR-TB (both relative to a scenario of no vaccine, and no improvement in RR-TB, i.e. status quo). Countries are denoted by their ISO alpha-3 codes and their corresponding full names are listed in Table 1. Colours for each country are only for the purpose of display, and do not designate any quantitative scale.

Fig. 5: Projected percent deaths from RR-TB averted, as a result of anti-TB vaccination.
figure 5

Rectangular bars show median estimates and error bars show 95% Bayesian credible intervals (CrIs), both estimated from n = 200 posterior samples for each country. As in Fig. 3, blue bars here show the vaccine-avertable proportions of rifampicin-resistant tuberculosis (RR-TB) deaths relative to a ‘status quo’ scenario, while adjacent bars show averted proportions in combination with ‘improved RR-TB management’, as outlined in the caption to Fig. 1. The latter bars are stratified to show: (i) the impact of improved management of RR-TB alone, i.e. in the absence of vaccination (orange segment), and (ii) the incremental impact of vaccination, acting in combination with these improvements (red segment). Error bars on the stacked orange and red bars show the 95% CrIs of the total impact of a vaccine combined with improved management of RR-TB. Countries are ranked in a descending order according to the number of RR-TB incident cases in 2018.

In all of these estimates we assumed the vaccine would have the same efficacy amongst individuals with and without human immunodeficiency virus (HIV) infection. Supplementary Table 2 shows sensitivity analyses when assuming that vaccine efficacy is reduced by half amongst those with HIV. Such a scenario shows only a modest effect on the global impact of vaccination on RR-TB: for example, with 10% (95% CrI: 9.7–11%) cases averted under the status quo scenario, being reduced to 10% (95% CrI: 9.5–11%).

Vaccine impact on antibiotic consumption

Supplementary Fig. 12 and Supplementary Table 3 additionally illustrate how vaccination reduces the total amount of second-line TB treatment needed, because of its impact on RR-TB. By contrast, efforts to improve the management of RR-TB would increase the demand for second-line drugs, as a result of increased identification of resistant cases (Supplementary Table 4). Finally, Supplementary Fig. 13 illustrates that future TB vaccines are likely to have only modest impact on antibiotic consumption beyond TB drugs, typically amounting to <1% of total estimated antibiotic consumption in each country. This limited impact arises because of the relative rarity of TB amongst those with respiratory symptoms receiving antibiotics, when compared against other aetiologies such as acute respiratory infections.


Our results suggest that an M72-like vaccine, when deployed as a post-exposure vaccine amongst adults and adolescents, could have an important impact on drug-resistant TB. Such a vaccine, acting alone, could avert 10% (95% CrI: 9.7–11%) of cumulative RR-TB cases over the next 15 years. Indeed, this impact is comparable to that of combining improvements in the management (detection and treatment) of RR-TB, projected to be 14% (95% CrI: 12–16%) of RR-TB cases over the same period (Table 2). The combined effect of vaccination and improved management is roughly additive (Figs. 3 and 5).

The impact of vaccination on relative reductions in RR-TB burden is roughly consistent across countries, reducing RR-TB cases between 5 and 16% (Fig. 2). Similar figures apply to relative reductions in RR-TB deaths (Fig. 4). In terms of country contributions to the projected global impact of vaccination, India and China are consistently the leading countries (Figs. 2 and 4), owing to their relatively large shares of global TB burden2. Countries in the former Soviet Union have the world’s highest rates of drug resistance amongst TB cases, however, their relative contributions to the global vaccine-avertable burden of RR-TB are lower, as a result of having smaller TB epidemics in absolute terms2.

We have presented results for the number of second-line TB treatments that would be avertable by a TB vaccine between 2020 and 2035, but a cost impact is outside the scope of this study. This is an important component of any costing analysis, because of the disproportionate cost of managing drug-resistant TB, for any national TB programme20,21. Notably, our results illustrate that—while vaccination could reduce the need for second-line drugs by reducing incidence of RR-TB—measures to improve the detection of RR-TB would have the opposite effect, by increasing the number of patients needing to be treated with second-line drugs (Supplementary Fig. 12). Appropriate TB treatment is critical for patient outcomes7,22. However, our results illustrate that a combined strategy—of vaccination with improved RR-TB management—could help to mitigate the budgetary burden on TB programmes, by reducing overall RR-TB burden while minimising the numbers of second-line treatments required (Table 2, Supplementary Fig. 12). Any resulting cost savings would release programmatic funds, potentially for other TB control efforts such as intensified case-finding that could—in turn—have a synergistic effect on reducing the burden of drug-resistant TB.

As a grounding example for our analysis, we have drawn data from the phase 2b trial of the M72/AS01E vaccine, which was limited to individuals with evidence of latent TB infection. Accordingly, we modelled a scenario where a vaccine is deployed solely for post-exposure protection, i.e. to reduce the risk of TB disease amongst those already infected. We expect that incorporating pre-exposure protection, and broadening eligibility to include all individuals regardless of infection status, would substantially increase the projected impact of vaccination. Future trial data will be valuable in informing these projections. Another important area for future work is the feasibility of, and best implementation strategies for, the type of mass vaccination programme considered here. School-based vaccination may be important in reaching 15-year-olds, and is already used for the delivery of tetanus and HPV vaccines in low- and middle-income countries23,24. To ensure equitable access, however, such strategies will need to be supplemented by additional measures such as mobile vaccine delivery, to reach those not in the school system. Supplementary analysis illustrates the importance of mass vaccination campaigns amongst adults, showing that without these additional efforts, overall impact on RR-TB incidence and mortality would drop by 85% (Supplementary Table 2). In practice, such catch-up efforts would need to be planned carefully: the existing coverage of adult immunisation in countries such as India presents substantial challenges25,26, which would likely apply to a future TB vaccine as well. In both types of vaccination effort, there are important considerations around whether the vaccine should be offered only to those with evidence of LTBI, or regardless. In the present work, we have assumed the former, a choice necessitated by the available data: the recent phase 2b trial of the M72/AS01E vaccine was restricted to those with LTBI14. As more data emerges about the effectiveness of the vaccine in uninfected individuals, an important area for further analysis would be the relative value of limiting vaccination coverage to those with LTBI (incurring the cost and effort of identifying these individuals), vs universal eligibility within defined age groups (incurring the cost of additional vaccinations). The per-dose cost of any future TB vaccine will likely be a driving factor in these considerations.

Another approach to prevention, currently part of WHO guidelines for programmatic management of TB, is the use of preventive therapy regimens amongst those known to have TB infection27. Although recent years have seen the emergence of shortened and simplified preventive therapy regimens9,10, these are rifampicin-based regimens, and thus unlikely to be effective against RR-TB infection. There is increasing recognition of the potential value of fluoroquinolone-based preventive regimens amongst contacts of those with known drug-resistant TB28,29 although there remains a pressing need for more clinical trials to demonstrate efficacy8. On the other hand, by preventing TB at the population level, not just amongst contacts of known cases, a future vaccine might have further-reaching impact than preventive therapy: however, a strategy, such as the one we have modelled here, may take several years to fully realise this impact (Supplementary Fig. 9). Any future strategy for TB prevention is, therefore, likely to require a combination of preventive therapy and vaccination.

In addition to mass vaccination, supplementary immunisation approaches may also have an important impact, for example, vaccination of close contacts of diagnosed TB cases. Recent modelling work (albeit in the context of preventive therapy) suggests that preventing 60% of incident TB amongst household contacts of TB cases in the WHO South-East Asian Region could reduce annual incidence rates in the Region by ~8%, by 203030. That analysis assumed preventive therapy to be ineffective amongst those with drug-resistant infection; a vaccine in place of preventive therapy, therefore, might be expected to have a similar impact on RR-TB, if not higher. Our analysis also does not address the potential use of therapeutic vaccination, that is administered following completion of treatment for active TB, in order to minimise the risk of recurrence31. By potentially reducing the risk of treatment-acquired drug resistance developing into active, infectious TB, such approaches could also have important implications for future RR-TB incidence.

Our focus on post-exposure vaccination amongst adults and adolescents with LTBI is motivated by the recent phase 2b trial of the M72 vaccine14, which suggested a 50% reduction in incidence amongst those receiving the vaccine. However, these numbers should be interpreted with caution, primarily because they come from a trial that was only designed to assess safety and immunogenicity, not efficacy; larger trials are needed to estimate protective efficacy with precision. Moreover, the protective effect was seen mostly after a year, in males and those under 25 years of age. The study was conducted in South Africa, Kenya and Zambia, settings with a high overall burden of TB (for example with South Africa having an annual TB incidence of 520 per 100,000 population2), and it is unclear how these findings might generalise to other settings. Therefore, phase 3 trial results in different settings will be invaluable in gaining more reliable estimates of efficacy. These limitations notwithstanding, our modelling results would apply generally to any post-exposure vaccine having 50% efficacy amongst adults and adolescents. For the purpose of our current study, the important findings reported in ref. 14 show that such a vaccine is indeed plausible.

As with any modelling analysis, our work has some limitations to note. For simplicity, and to cover 30 countries in a systematic way, we captured key features of TB transmission with four different model structures, using country-specific calibrations. Some model parameters are subject to substantial uncertainty, such as the quality of TB care in the private healthcare sector; we have aimed to address this uncertainty by adopting wide uncertainty intervals for these parameters (Supplementary Table 5), and by propagating this uncertainty to model projections using Bayesian calibration methods. For simplicity we adopted a simple model mechanism for ageing, assuming a constant per-capita hazard of transitioning between child and adult strata. This simplification allows us to accommodate additional, country-specific complexities such as public and private healthcare providers, and the role of HIV in driving TB dynamics. Nonetheless, our results for TB impact remain broadly consistent with those reported in earlier studies which use more complex demographic structure12. In the case of China, where most TB burden is concentrated in those aged over 65 years, additional sensitivity analysis suggests that model results do not change substantially, with the inclusion of a third age group to represent the elderly (Supplementary Fig. 14). Our model also entails simplifications around HIV and TB, adopting a relatively simple HIV care cascade (Supplementary Fig. 15c), as well as borrowing from previous work32 to incorporate simplified scenarios for the scale-up and maintenance of antiretroviral treatment (ART) (Supplementary Methods 1). Sensitivity analysis suggests that the influence of HIV on effectiveness of a future TB vaccine would have important implications for vaccine impact in countries with high HIV burden but would not substantially change our estimates for vaccine impact at the global level (Supplementary Table 2).

Such limitations notwithstanding, the essential findings of our analysis are likely to hold true: that an M72-like vaccine, even with an efficacy of only 50%, at 72–76% coverage of LTBI adolescents and adults, would have an important impact on the global burden of RR-TB, as well as important synergistic effects with ongoing efforts to improve the detection and treatment of RR-TB. As with many challenges in TB control, optimal control strategies in the future are likely to involve a combination of different approaches: our work illustrates the critical role that vaccination could play, as part of these strategies.


Model structure

We limited our analysis to the 30 countries shown in Table 1 and Supplementary Fig. 16, which together accounted for 90% of global RR-TB incidence in 20182. To account for the wide variation in TB epidemiology and health systems between these different countries, we developed four different TB models, relating to each of the categories shown in Table 1, and described in further detail in Supplementary Methods 1. For countries where HIV is a driving factor in TB burden (Supplementary Fig. 17), we modelled the historical dynamics of HIV using data obtained from The Joint United Nations Programme on HIV/AIDS (UNAIDS)33. We also modelled the impact of HIV on TB progression, as well as the mitigating effect of ART and isoniazid preventive therapy for TB (assuming such preventive therapy to be effective only against drug-sensitive infection). We did not explicitly model the dynamics of HIV and ART, instead taking these as model inputs. For countries where the private sector has a substantial presence, we distinguished between those receiving care in the public and private sectors, and assumed a lower standard of TB care in the latter than in the former34,35,36,37. Given little systematic data for care provided by the private sector in different countries, we adopted broad uncertainty intervals for the accuracy of TB diagnosis and for treatment completion rates in this sector.

For each of four TB models we stratified the population into those above and below 15 years of age, and modelled ageing as a constant rate-of-transition between these strata, chosen to capture the country demographics as of 201838. Model equations and parameters can be found in Supplementary Methods 1, Supplementary Fig. 15, and Supplementary Tables 5, 6.

Data and calibration

For each country we calibrated the model to a range of epidemiological and programmatic indicators, including the WHO estimates for TB incidence and mortality, stratified by age group; the proportion of incident TB cases being RR-TB; and the proportion of TB incidence that occurred in those coinfected with HIV (Supplementary Table 7). For countries having a strong private sector healthcare presence, we assumed that all those surviving to the point of care-seeking are managed by either the public or private sector: by combining data for public sector notifications with model projections for incidence and mortality, therefore, we aimed to estimate the proportion of patients being managed by the public vs private sectors. For countries with a driving role of HIV in the TB epidemic, we obtained ART coverage from UNAIDS, for simplicity assuming a linear scale-up to current levels32. We calibrated the model using Adaptive Markov Chain Monte Carlo39, which allows systematic propagation of uncertainty from model inputs to model projections, while updating the proposal distribution at each iteration. We reduced autocorrelation by taking every 150th sample and discarded the first 20,000 samples, to yield 200 samples overall (Supplementary Methods 2). We calculated 2.5th and 97.5th percentiles as the 95% credible intervals, and the 50th percentile as point estimates, on these samples and on model projections. As a form of model validation, we compared model projections for TB prevalence to findings from prevalence surveys, where available. For any countries where model-projected prevalence did not match those from the prevalence surveys (in particular, where the uncertainty intervals did not overlap), we recalibrated the models using the prevalence survey data, to ensure consistency with all available information.

Intervention simulations

Consistent with the WHO preferred product characteristics13 and the outcome of the M72/AS01E trial14, we assumed that the effect of the vaccine is to attenuate the rates of primary progression and reactivation of latent TB amongst adults and adolescents, thereby reducing TB incidence rates amongst those vaccinated by 50%. We did not consider the vaccine protection against recurrence of TB. We assumed an average duration of protection of 10 years, and that after this period, vaccinated individuals revert to their unvaccinated status of LTBI. In the main analysis, we assumed for simplicity that the effectiveness of a future TB vaccine would be unaffected by the HIV status of recipients. Currently, there is no evidence for the effect of HIV coinfection on the performance of M72-like vaccines, as the recent phase 2b trial was limited to HIV-negative individuals. However, the RTS,S malaria and pneumococcal conjugate vaccines offer examples of vaccines whose effectiveness is impaired by HIV40,41. Therefore, as a sensitivity analysis, we modelled a scenario where a future TB vaccine has half the efficacy amongst HIV positive individuals, compared to those without HIV.

We assumed a routine TB immunisation programme which vaccinates adolescents on their 15th birthday from 2025 to 2035, with country-specific vaccination coverage derived from secondary school attendance42 (Supplementary Fig. 18). In addition, to boost vaccine coverage among all adults over 15 years old, we assumed 2-year catch-up campaigns, implemented every 5 years, with a peak coverage of 72–76%, according to WHO region12. The peak coverage of these campaigns was derived from earlier modelling work12, where the data were extracted from previous rubella vaccination campaigns and adapted to a wider target population of adults and adolescents. We projected the averted cumulative incidence of RR-TB; the averted cumulative deaths; and the averted patient-months of second-line TB treatment over 2020–2035. We assessed these outcomes with respect to a ‘status quo’ comparator, assuming current TB services continue indefinitely without change. We also considered an ‘improved RR-TB management’ comparator, reflecting ongoing improvements in the management of RR-TB, in particular assuming that 85% of TB diagnoses also receive drug susceptibility testing for rifampicin resistance (for example, through the increased use of molecular diagnostic tools19), and that second-line treatment success is increased to 75% (resulting from adoption of new, second-line regimens5), from 2020 onwards. Supplementary Fig. 10 shows these indicators of RR-TB management in relation to the levels currently reported by different countries.

Potential contribution to control of antibiotic consumption

Unnecessary antibiotic consumption is a key driver of antimicrobial resistance, more broadly than TB. We additionally examined the potential for a future TB vaccine to reduce this consumption through the bystander effect43: that is, as a result of reducing symptomatic presentations for primary care, and thus reducing instances of empiric antibiotic treatment. We used data from Demographic Health Surveys (DHS)44, for the proportion of acute respiratory illness that is medically attended and treated with antibiotics in different settings, together with estimates from the Global Burden of Disease 2017 project45 for all-cause incidence of respiratory disease in the same countries as those covered in the DHS data (Supplementary Methods 3).

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

Country-specific data used in this study are publicly available and their sources are summarised in Supplementary Table 7, including population statistics from the United Nations World Prospect Project 2019 (; TB incidence, mortality, and other programmatic indicators from the WHO Global Tuberculosis Database (; HIV prevalence and ART coverage from the data tool of UNAIDS (; and secondary school attendance from the United Nations Children’s Fund ( For analysis of antibiotic consumption for cough-related diseases, data were obtained from the DHS Program (, through the rdhs 0.6.3 package in R 4.0.2) and the Global Burden of Disease Study 2017 ( Extracted data are also presented in Supplementary Table 7 or available at data are provided with this paper.

Code availability

MATLAB codes for simulating TB dynamics and vaccine impacts are available at


  1. Dheda, K. et al. The Lancet Respiratory Medicine Commission: 2019 update: epidemiology, pathogenesis, transmission, diagnosis, and management of multidrug-resistant and incurable tuberculosis. Lancet Respir. Med. 7, 820–826 (2019).

    CAS  Article  Google Scholar 

  2. World Health Organization. Global tuberculosis report 2019. (2019).

  3. Gandhi, N. R., Brust, J. C. M. & Shah, N. S. A new era for treatment of drug-resistant tuberculosis. Eur. Respir J. 52, (2018).

  4. Nunn, A. J. et al. A trial of a shorter regimen for rifampin-resistant tuberculosis. N. Engl. J. Med. 380, 1201–1213 (2019).

    CAS  Article  Google Scholar 

  5. World Health Organization. WHO consolidated guidelines on drug-resistant tuberculosis treatment. (2019).

  6. Lange, C. et al. Perspectives for personalized therapy for patients with multidrug-resistant tuberculosis. J. Intern. Med. 284, 163–188 (2018).

  7. Zurcher, K. et al. Drug susceptibility testing and mortality in patients treated for tuberculosis in high-burden countries: a multicentre cohort study. Lancet Infect. Dis. 19, 298–307 (2019).

    CAS  Article  Google Scholar 

  8. Fox, G. J. et al. Preventing the spread of multidrug-resistant tuberculosis and protecting contacts of infectious cases. Clin. Microbiol. Infect. 23, 147–153 (2017).

    CAS  Article  Google Scholar 

  9. Swindells, S. et al. One month of rifapentine plus isoniazid to prevent HIV-related tuberculosis. N. Engl. J. Med. 380, 1001–1011 (2019).

    CAS  Article  Google Scholar 

  10. Sterling, T. R. et al. Three months of rifapentine and isoniazid for latent tuberculosis infection. N. Engl. J. Med. 365, 2155–2166 (2011).

    CAS  Article  Google Scholar 

  11. Kaufmann, S. H., Weiner, J. & von Reyn, C. F. Novel approaches to tuberculosis vaccine development. Int. J. Infect. Dis. 56, 263–267 (2017).

    Article  Google Scholar 

  12. Knight, G. M. et al. Impact and cost-effectiveness of new tuberculosis vaccines in low- and middle-income countries. Proc. Natl. Acad. Sci. USA 111, 15520–15525 (2014).

    ADS  CAS  Article  Google Scholar 

  13. World Health Organization. WHO preferred product characteristics for new tuberculosis vaccines. (2018).

  14. Tait, D. R. et al. Final analysis of a trial of M72/AS01E vaccine to prevent tuberculosis. N. Engl. J. Med. 381, 2429–2439 (2019).

    CAS  Article  Google Scholar 

  15. Pai, M., Daftary, A. & Satyanarayana, S. TB control: challenges and opportunities for India. Trans. R. Soc. Tropical Med. Hyg. 110, 158–160 (2016).

    Article  Google Scholar 

  16. McDowell, A. & Pai, M. Treatment as diagnosis and diagnosis as treatment: empirical management of presumptive tuberculosis in India. Int. J. Tuberc. Lung D. 20, 536–543 (2016).

    CAS  Article  Google Scholar 

  17. Satyanarayana, S. et al. Use of standardised patients to assess antibiotic dispensing for tuberculosis by pharmacies in urban India: a cross-sectional study. Lancet Infect. Dis. 16, 1261–1268 (2016).

    Article  Google Scholar 

  18. von Gottberg, A. et al. Emergence of levofloxacin-non-susceptible Streptococcus pneumoniae and treatment for multidrug-resistant tuberculosis in children in South Africa: a cohort observational surveillance study. Lancet 371, 1108–1113 (2008).

    Article  Google Scholar 

  19. Weyer, K. et al. Rapid molecular TB diagnosis: evidence, policy making and global implementation of Xpert MTB/RIF. Eur. Respir. J. 42, 252–271 (2013).

    Article  Google Scholar 

  20. Gunther, G., Gomez, G. B., Lange, C., Rupert, S. & van Leth, F., Tbnet. Availability, price and affordability of anti-tuberculosis drugs in Europe: a TBNET survey. Eur. Respiratory J. 45, 1081–1088 (2015).

    Article  Google Scholar 

  21. Pooran, A., Pieterson, E., Davids, M., Theron, G. & Dheda, K. What is the cost of diagnosis and management of drug resistant tuberculosis in South Africa? PLoS ONE 8, e54587 (2013).

  22. Cox, H. & Mizrahi, V. The coming of age of drug-susceptibility testing for tuberculosis. N. Engl. J. Med. 379, 1474–1475 (2018).

    Article  Google Scholar 

  23. Bundy, D. A. P. et al. Investment in child and adolescent health and development: key messages from Disease Control Priorities, 3rd edition. Lancet 391, 687–699 (2018).

    Article  Google Scholar 

  24. Wigle, J., Coast, E. & Watson-Jones, D. Human papillomavirus (HPV) vaccine implementation in low and middle-income countries (LMICs): health system experiences and prospects. Vaccine 31, 3811–3817 (2013).

    Article  Google Scholar 

  25. Dash, R. et al. Towards adult vaccination in India: a narrative literature review. Hum. Vaccin. Immunother. 16, 991–1001 (2020).

    Article  Google Scholar 

  26. Tan, L. J. Adult vaccination: now is the time to realize an unfulfilled potential. Hum. Vaccin. Immunother. 11, 2158–2166 (2015).

    Article  Google Scholar 

  27. World Health Organization. WHO consolidated guidelines on tuberculosis: module 1: prevention: tuberculosis preventive treatment. (2020).

  28. Fox, G. J., Oxlade, O. & Menzies, D. Fluoroquinolone therapy for the prevention of multidrug-resistant tuberculosis in contacts. A cost-effectiveness analysis. Am. J. Respir. Crit. Care Med. 192, 229–237 (2015).

    CAS  Article  Google Scholar 

  29. Malik, A. A. et al. Tuberculosis preventive therapy for individuals exposed to drug-resistant tuberculosis: feasibility and safety of a community-based delivery of fluoroquinolone-containing preventive regimen. Clin. Infect. Dis. 70, 1958–1965 (2020).

    ADS  CAS  Article  Google Scholar 

  30. Mandal, S., Bhatia, V., Sharma, M., Mandal, P. P. & Arinaminpathy, N. The potential impact of preventive therapy against tuberculosis in the WHO South-East Asian Region: a modelling approach. BMC Med. 18, 163 (2020).

    Article  Google Scholar 

  31. Vekemans, J. et al. Preferred product characteristics for therapeutic vaccines to improve tuberculosis treatment outcomes: Key considerations from World Health Organization consultations. Vaccine 38, 135–142 (2020).

    CAS  Article  Google Scholar 

  32. Vesga, J. F. et al. Assessing tuberculosis control priorities in high-burden settings: a modelling approach. Lancet Glob. Health 7, e585–e595 (2019).

    Article  Google Scholar 

  33. UNAIDS. AIDSinfo. (2020).

  34. Das, J. et al. Use of standardised patients to assess quality of tuberculosis care: a pilot, cross-sectional study. Lancet Infect. Dis. 15, 1305–1313 (2015).

    Article  Google Scholar 

  35. Sreeramareddy, C. T., Qin, Z. Z., Satyanarayana, S., Subbaraman, R. & Pai, M. Delays in diagnosis and treatment of pulmonary tuberculosis in India: a systematic review. Int. J. Tuberc. Lung Dis. 18, 255–266 (2014).

    Article  Google Scholar 

  36. Wells, W. A., Uplekar, M. & Pai, M. Achieving systemic and scalable private sector engagement in tuberculosis care and prevention in Asia. PLoS Med. 12, e1001842 (2015).

    Article  Google Scholar 

  37. Uplekar, M. Public-private mix for tuberculosis care and prevention. What progress? What prospects? Int. J. Tuberc. Lung Dis. 20, 1424–1429 (2016).

    CAS  Article  Google Scholar 

  38. United Nations Deparatment of Economic and Social Affairs. World Population Prospects. (2019).

  39. Haario, H., Saksman, E. & Tamminen, J. An adaptive Metropolis algorithm. Bernoulli 7, 223–242 (2001).

    MathSciNet  Article  Google Scholar 

  40. Otieno, L. et al. Safety and immunogenicity of the RTS,S/AS01 malaria vaccine in infants and children identified as HIV-infected during a randomized trial in sub-Saharan Africa. Vaccine 38, 897–906 (2020).

    CAS  Article  Google Scholar 

  41. Klugman, K. P. et al. A trial of a 9-valent pneumococcal conjugate vaccine in children with and those without HIV infection. N. Engl. J. Med. 349, 1341–1348 (2003).

    CAS  Article  Google Scholar 

  42. United Nations Children’s Fund. UNICEF Data: Secondary education. (2019).

  43. Lipsitch, M. & Siber, G. R. How can vaccines contribute to solving the antimicrobial resistance problem? Mbio 7, (2016).

  44. ICF. The DHS Program Data. (2019).

  45. Global Burden of Disease Collaborative Network. Global Burden of Disease study 2017 (GBD 2017) results. (2018).

  46. World Health Organization. Public–private mix for TB prevention and care: a roadmap. (2018).

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This work is funded by the Bill & Melinda Gates Foundation (OPP1190803). H.F. and N.A. also acknowledge the Centre funding (MR/R015600/1) jointly from the UK Medical Research Council (MRC) and the UK Foreign, Commonwealth & Development Office (FCDO), under the MRC/FCDO Concordat agreement and also within the scope of the EDCTP2 programme supported by the European Union.

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R.L. and N.A. conceived the study. H.F. and N.A. developed the models, curated research data, and performed the analysis. J.L., I.F. and R.L. provided validation of study findings and input on model design. H.F. and N.A. prepared the first draft of the manuscript, and all authors contributed to the revised manuscript.

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Correspondence to Han Fu.

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Fu, H., Lewnard, J.A., Frost, I. et al. Modelling the global burden of drug-resistant tuberculosis avertable by a post-exposure vaccine. Nat Commun 12, 424 (2021).

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