Enteric fever (commonly known as typhoid fever) is a bacterial disease caused by Salmonella Typhi. It is spread through the ingestion of food or drink contaminated by the feces or urine of infected people. It is usually characterized by fever, headache, constipation, and malaise, but it has few symptoms that reliably distinguish it from other infectious diseases, which makes it difficult to diagnose and treat. Symptoms range from mild to severe, and can even result in death.
Because it is difficult to diagnose typhoid, estimates for the numbers of typhoid cases and deaths vary but 21 million cases of typhoid fever and 200,000 deaths are estimated to occur worldwide. Like cholera, it occurs in low-income settings with poor sanitation and hygiene, and lack of clean water. Infants and young children in particular are at risk.
There are several typhoid vaccines on the market: the live oral Ty21a vaccine, mainly used as a traveler’s vaccine; the injectable Vi polysaccharide vaccine (Vi vaccine); and the Vi polysaccharide tetanus toxoid conjugate vaccine (Typbar; produced by Bharat Biotech). However there are limitations that preclude their use in developing countries.
IVI’s Enteric Fever Program aims to accelerate the development and introduction of safe, effective and affordable typhoid conjugate vaccines to prevent and control typhoid in developing countries. We are using the experiences and lessons learned from our work in cholera to accelerate the development and delivery of a new vaccine against typhoid. A public-private partnership approach with partners from from Korea, Indonesia, Bangladesh, and the U.S is being used to make a new typhoid vaccine accessible and available to populations that desperately need it.
IVI has completed development of a typhoid conjugate which consists of the Vi polysaccharide purified from Salmonella Typhi chemically conjugated to diphtheria toxoid (DT). Compared with Vi typhoid vaccines, this new typhoid conjugate vaccine (Vi-DT) promises to protect infants less than two years of age as well as young children against typhoid fever and provide a longer duration of protection.
IVI has now transferred the technology for production and quality control of Vi-DT to three manufacturing partners and will now assist with the development of a clinical plan and performance of clinical trials required for licensure and WHO prequalification. As with all of IVI’s vaccine technology transfer partnerships global access agreements have been signed to ensure high quality affordable vaccine for use in public-sector markets. IVI continues to work with two of our partners – SK Chemicals of Korea and BioFarma of Indonesia – to finalize clinical development plans and it is anticipated that the clinical trials with both companies will begin in 2016. In addition, Vi-DT technologies were transferred to Incepta Vaccine Ltd of Bangladesh in 2014.
IVI has also been developing a functional serum bactericidal assay that should help answer questions concerning vaccine efficacy and correlates of protection and hopefully will simplify the pathway to licensure and WHO prequalification of the IVI’s and other Vi conjugate vaccines.
Having three manufacturers of the typhoid vaccine will help ensure a sufficient and cost-competitive supply for the global market. The vaccine is expected to be licensed and WHO prequalified in readiness for global use as early as 2019.
A New Bivalent Enteric Fever Conjugate Vaccine on the Horizon
We are also developing a conjugate vaccine to protect against typhoid and paratyphoid fever. There is reportedly a high burden of paratyphoid fever in South Asia therefore a single vaccine that can protect against both diseases would be extremely beneficial. IVI has developed new conjugation methodologies for the paratyphoid conjugate. A bivalent (typhoid/paratyphoid A) candidate is in the preclinical phase, and plans will be made for technology transfer to a manufacturer soon.
Generating Evidence on the Burden of Typhoid
From 2011 to 2014, we conducted typhoid surveillance among a network of 13 field sites in ten sub-Saharan African countries through the Typhoid Surveillance in Africa Program (TSAP). While anecdotes suggest that typhoid is a problem in Africa, there were limited scientific data to back up those claims. TSAP, funded by the Bill & Melinda Gates Foundation, was established to generate scientific data on the epidemiology of typhoid in Africa.
TSAP results show a significant burden of typhoid in Ghana, Kenya, Madagascar and Burkina Faso; yet non-typhoidal Salmonella infection may be more of a problem than S. Typhi, particularly in Plasmodium falciparum malaria-endemic settings. In addition, multi-drug resistance is a concern and severe typhoid cases are seen in rural settings. Based on these findings, IVI is moving to the next research phase, which will look at the outcomes of severe typhoid cases in Africa – Severe Typhoid in Africa Program (SETA).
SETA, supported by the Bill & Melinda Gates Foundation, will continue and expand the collection of data from the typhoid fever surveillance network established in TSAP. SETA will continue to collect standardized disease burden data from various sub-Saharan African countries, several of which were in TSAP.
SETA will collect additional information on invasive Salmonella infections such as long-term manifestations of illness and socio-economic burden. Samples will be collected from patients to measure their immune system response as well as describe the carrier states of Salmonella infections. Evidence from SETA will continue to strengthen the case for prevention and control measures, including the introduction of vaccines against typhoid/paratyphoid and non-typhoidal Salmonella infections.
We gratefully acknowledge the Governments of the Republic of Korea and Sweden, and the Bill & Melinda Gates Foundation for their support.