Persistent infections are GOOD for you: Sickly people will end up having stronger immune system in old age 

  • Researchers found lingering infections strengthen the body's defenses
  • It means people with repeated bouts of herpes or TB will end up stronger
  • The findings could pave the way to 'active' vaccines that keep testing the body 

Sickly people are seen as weak, constantly succumbing to repeated infections. 

But new research suggests they will have the last laugh - as their immune systems will be stronger in later life.

Persistent illnesses are essentially training the body, ultimately building up long-term immunity, according to a study by Washington University School of Medicine.

Experts say the findings show a need for 'long-lasting' vaccinations that continually release traces of the infection.

But scientists have no idea how we do that without causing mass outbreaks of easily-spread infections.

The research, published today in Proceedings of the National Academy of Sciences, specifically focuses on leishmaniasis as an example. 

Leishmaniasis, a tropical disease that kills tens of thousands of people every year, is caused by a parasite. 

The researchers found that by constantly reminding the immune system what the parasite that causes leishmaniasis looks like, a persistent infection kept the immune system on alert against new encounters. 

This, they believe, would be the same for immune systems constantly bombarded by bacteria responsible for tuberculosis or viruses that lead to herpes and chickenpox. 

'People had been thinking of the role of the immune system in persistent infection in terms of mowing down any pathogens that reactivate in order to protect the body from disease,' said Dr Stephen Beverley, the Marvin A. Brennecke Professor of Molecular Microbiology and the study's senior author.

'What was often overlooked was that in the process of doing this, the immune system is constantly being stimulated, which potentially promotes protection against future illness.' 

His co-author Dr Michael Mandell added: 'A lot of pathogens cause persistent infections, but the process was something of a black box. 

'Nobody really knew what was going on during persistent infection and why it was associated with immunity.'

To find out, Mandell and Beverley studied Leishmania, a group of parasites that cause ulcers on the skin and can infect internal organs. 

An estimated 250 million people worldwide are infected with the parasite - found in tropical areas - and 12 million have active disease. 

The disease can be disfiguring or even fatal, but once a person is infected, he or she is protected from getting sick a second time. 

In other words, infection confers long-term immunity.

People are thought to continue to harbor the parasite at low numbers for years after they recover from the disease, including some people treated with anti-leishmania drugs. 

This persistence may be to the benefit of their human hosts; studies in mice have shown that completely clearing the parasite often makes the animals susceptible to another bout of disease if they encounter the parasite again.

Studying mice, the researchers used fluorescent markers to distinguish different types of mouse cells, and found that most of the parasites live in immune cells capable of killing the parasites. 

Yet, despite their dangerous homes, the parasites appeared normal in shape and size.

Further, most of the parasites continued to multiply, yet the total number of parasites stayed the same over time.

'Mike Mandell called it the 'Jimmy Hoffa effect' because we couldn't locate the body,' Dr Beverley said. 

'We were unable to show directly that the parasites were being killed. But some of them must have been dying because the numbers weren't going up.'

The immune cells that housed the parasites are responsible for killing pathogens and activating a more robust immune response. 

It is this process - the ongoing multiplication and killing of parasites - that the researchers believe underlies the long-term immunity associated with persistent infection, explaining why people typically can't get sick with the same pathogen twice.

'It seems that our immunologic memory needs reminding sometimes,' Dr Mandell said. 

'As the persistent parasites replicate and get killed, they are continually stimulating the immune system, keeping it primed and ready for any new encounters with the parasite.'

These findings suggest that there are benefits as well as dangers to persistent infection, and, for some organisms at least, developing a vaccine that elicits life-long immunity might require a live vaccine that has the ability to persist without sickening people.

'Usually scientists design vaccines to get sterilizing immunity. They're trying to just kill all the bugs,' Dr Beverley said. 

'But what you really need is protection against the pathologic consequences of the disease, not necessarily sterilizing immunity. For some of these organisms, solid, long-term protection may come at the price of persistent infection.'

 

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