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Why TB Vaccines Should Be a Top Priority

 

Guest Blog by John Godwin, International Development Consultant & Australia Representative for Aeras, a non-profit product development organization dedicated to the development of effective tuberculosis (TB) vaccines and biologics to prevent TB. 

TB should be a priority for AusAID because of the high burden of disease in Asia and the Pacific. Eight low and middle-income countries in the Asia Pacific region – Bangladesh, Cambodia, China, India, Indonesia, the Philippines, Thailand and Vietnam – are among the 22 countries with the highest burdens of TB globally.

Earlier last month, AusAID released a Draft Medical Research Strategy to guide funding of medical research. AusAID’s initial priorities will be funding product development partnerships (PDPs) for malaria and TB research. This is great news and comes at a time when so many other donor governments are cutting back due to the financial downturn.

The current TB vaccine, BCG, has not been effective in curbing the TB epidemic, leaving TB To continue having enormous public health impacts. The spread of drug resistant strains is an alarming development. Globally, approximately 440,000 new cases of multidrug resistant TB (MDR-TB) occur each year, killing more than a third of its victims. Most worryingly, MDR-TB has gone from being the result of poor adherence to frontline drugs, to primary transmission in a significant proportion of cases.The only way to stop the spread of TB is to prevent its emergence. In this regard, the most cost- effective weapon would be a vaccine that prevents adolescents and adults from developing the disease. Newer TB vaccines that will either replace or boost BCG are being developed and a number of these have entered late stage clinical trials. 

The new AusAID Strategy presents an opportunity for Australia to provide leadership in vaccine research. However, concerns have arisen that one aspect of the Draft Strategy may severely limit AusAID’s ability to play a lead role in this critical area. The Draft Strategy proposes a condition that research will only be funded if there is “a short time (up to 5 years) to an outcome for poor people”.

In the vaccine development field, the requirement of a new product in less than five years is unduly restrictive. Imposing a strict five-year timeframe does not take into account the time required to enrol more than 20,000 participants in a Phase III trial and conduct the necessary follow-up. That said, the global epidemic will continue to spread, costing the health system and the global economy billions each year without a vaccine.

Until recently little attention or investment had been devoted to new TB vaccines. However, tremendous progress has been made in the past 10 years. The pipeline has grown from a single vaccine candidate in clinical testing in 2000, to now more than 12. Development of new TB vaccines is at a crucial juncture right now with a number of candidates in late stage trials. With sufficient support from governments, private donors and industry partners, we will be able to sustain this momentum toward an improved vaccine to prevent TB by 2020.

Australia is home to a robust network of TB researchers that can be leveraged to accelerate global TB vaccine development. For example, researchers at the Centenary Institute at Sydney University are providing global leadership in aspects of TB vaccine research and are important partners.

Over the past 25 years, there has been a significant increase in funding for TB research, with support from the Bill & Melinda Gates Foundation and the US, UK, Dutch, British, Norwegian,and other European governments. Mass vaccination campaigns would save millions of people from TB-related morbidity and mortality and would benefit economies. It would also protect countries where TB is not currently endemic, for example, Australia, from the threat of drug- resistant TB.

There is a risk that reduced funding for TB vaccine research as a result of reduced donor budgets may see the R&D effort lose momentum. Australian participation alongside other donors in funding the vaccine development effort would help accelerate progress, and build on AusAID’s leadership role in tackling the Asia Pacific region’s major health challenges. With the finalization of the Medical Research Strategy, AusAID should commit funding to the multinational global TB vaccine effort, particularly since almost a third of the world’s MDR-TB burden is in the Western Pacific region.

The world simply cannot afford to not invest in the ultimate weapon against TB – a vaccine.

*Image from Aeras homepage

Posted by John Godwin in Global Health for column GPP - Australia on Sep 3rd 2012, 13:05

Comments

11/09/12 9:28am - Posted By Rhea Coler, IDRI - Flag as inappropriate - Reply to this comment
There are many challenges ahead in this field including funding, clinical trial designs, and advancing candidates from early safety & immunogenicity trials to proof-of-concept efficacy trials. In the last decade much progress has been made in the field of TB vaccine development, and we have reason to be optimistic about the prospects for a TB vaccine that is more effective than the current BCG vaccine. We have a rich pipeline of at least 15 new candidate vaccines that have entered into clinical testing, including ID93/GLA-SE which was developed by IDRI.
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There's no question that sestnciits are often ineffective at communicating about their work outside of their field, and if they were better at this some of the confusion might be avoided. Carl Sagans and Neil de Grasse Tysons are rare. Still, there's a reason why physicists become physicists instead of journalists, and why journalists write for newspapers instead of working in physics labs. It is probably not reasonable to expect those in such different fields to have the same skill sets. It is no more apropriate to say sestnciits should just communicate better than it is to say journalists should just understand math better. And jargon is not arbitrary or purposeless. It develops because, within the field that generates it, it has a function it communicates an idea with greater clarity and precision, and often brevity, than ordinary colloquial English. I can say the results of the Student's T-test show the difference in means between groups is not due to chance, or I can say the difference is statistically significant, or even just significant. When talking to colleagues, it is clearly more efficient to use the shorthand, and it is understandable that having to then translate this into longer, clumsier language for the benefit of the lay public can be an irksome or difficult chore for many sestnciits.My purpose in posting this list was not to lay blame for the often poor communication between sestnciits and the general public, but to point out some examples of one phenomenon which contributes to this problem; the variable meaning of words in quotidian and technical usage. The same kind of meaning variability applies to language in general, and it is probably unavoidable. Different groups, defined by class, ethnicity, region, education level, profession, and many other such criteria, will use the same words in different ways, and confusion may result. Hopefully, in the case of sestnciits communicating with non-scientists, making both sides aware of the way some words differ in their general and technical usage can help to mitigate the communication problem a little bit.
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The definition of an aiangenictlly shifted flu virus' changed subtly with the H1N1 swine pandemic'. Prior to 2009, the term shift' was applied when a new' H-type appeared (or reappeared, after not having been circulating for many years) and pandemics were associated with a change in circulating H-type (probably H3 to HI with the Spanish flu in 1918-19, H1 to H2 with the Asian flu in 1956-57, H2 to H3 with the Hong Kong flu in 1968-69). H1 viruses had been circulating since 1976 (why wasn't that reappearance designated a pandemic some textbooks, eg Mandel et al, DO count it but there wasn't an enormous loss of life as in 1918-19, 1956-57 or 1968-69, so maybe that is why it is largely ignored and not counted as a pandemic). The H1N1 swine was a mild infection for most (not to underestimate the impact it had for those who had more severe illnesses and the people who died) and might have qualified as a drifted' virus in earlier years. There have been other years when a drifted' virus has caused more morbidity and mortality than H1N1 swine (eg the 1989-90 H3 virus in the UK, at least).But a universal vaccine (irrespective of the semantics around pandemics) would be very welcome declaration of interest: I am approaching my elder years, when flu becomes more of a threat, and I welcome anything I can get especially a vaccine to try to keep me healthy!
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