Chagas Disease vaccine works in mice

Trypanosoma cruzi Chagas disease, caused by Trypanosoma cruzi and transmitted by insects in Latin America is among the most common tropical diseases, and so far without effective vaccine. A new study published in PLOS Pathogens shows that a candidate vaccine can induce long-lasting immunity against the parasite in mice.

The relatively mild acute phase of Chagas disease is followed by the more dangerous chronic phase, during which parasites take up residence in the host, mostly in the heart and stomach muscles. About a third of infected people (presumably those with higher chronic parasite numbers) develop serious heart disease or digestive tract complications many years after the initial infection. An ideal Chagas vaccine would prevent infection altogether, but one that prevents the complications during the chronic phase by keeping parasite numbers low would eliminate most of the disease burden.

Researchers had previously shown that a vaccine that contains three particular parasite proteins is a good candidate: Mice that were infected with T. cruzi immediately after vaccination were able to keep parasite numbers down during the acute infection and showed none of the inflammation in muscle tissue seen after infection of un-vaccinated mice. In this study, the researchers tested whether the vaccinated mice would be protected in the long run. To do this, they vaccinated mice with a combination of two of the T. cruzi proteins (TcG2 and TcG4), which they had shown to be the most potent in provoking both an antibody and a T-cell immune response.

The vaccination was done in two steps: the first injection contained DNA coding for the TcG2 and TcG4 proteins, and the second, three weeks later, a mix of the two proteins themselves (D/P regimen). Some mice were also given a booster immunization three months later, which consisted again of a mix of the two proteins (D/P/P regimen). Even without the booster shot, the D/P regimen caused long-lasting, T. cruzi-specific, changes in the immune system. The vaccine generated a pool of TH1 CD4+T cells (also called helper T cells) that are necessary for an effective antibody response as well as a stable pool of CD8+T memory cells. Both pools rapidly expanded when mice were infected with T. cruzi four months after vaccination, and the vaccinated mice were able to keep parasite numbers 2-3 fold lower than unvaccinated infected mice.

Mice that had received the booster shot at three months (D/P/P regimen) and were infected four months later had an even more potent immune response: their parasite numbers were about 5-fold lower than those of unvaccinated controls. The vaccine-induced immunity waned slightly six months after the booster immunization, but was still sufficient to provide 2-fold control of invading pathogens. This should be sufficient to break the parasite transmission cycle (i.e. biting insects don’t pick up enough parasites to infect the next host) and prevent chronic disease symptoms in the vaccinated host.

The TcG2/TcG4 D/P vaccine provided long-term anti-T. cruzi T cell immunity, and booster immunization would be an effective strategy to maintain or enhance the vaccine-induced protective immunity against T. cruzi infection and Chagas disease. The next steps toward clinical studies in humans include characterizing the quality and quantity of immunity to the vaccine candidates in naïve individuals.

A Two-Component DNA-Prime/Protein-Boost Vaccination Strategy for Eliciting Long-Term, Protective T Cell Immunity against Trypanosoma cruzi. (2015) PLoS Pathog 11(5): e1004828. doi:10.1371/journal.ppat.1004828

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