Researchers follow two main approaches to an HIV vaccine: antibodies and T cells. Antibodies, proteins produced by the immune system to identify and neutralize foreign objects, were big in the early years of the research, but after disappointing results interest moved to responses conducted by immune cells. This changed again with the discovery of broadly neutralizing antibodies, which are produced by 20 percent of HIV-positive individuals two or three years after infection. These antibodies are able to target specific regions of the virus that are important for its survival and are present in many of the different HIV subtypes. So a vaccine comprising them might be effective despite the virus’s variability, a problem that has been a considerable hurdle. They are so promising, researchers at the meeting said, that one of the recommended therapeutic approaches is to inject the antibodies directly into the bloodstreams of those at risk. Although these antibodies have been used to treat specific illnesses, they have not been considered as a vaccine substitute for the broad population. Another strategy is to use the parts of the HIV virus these antibodies recognize as models to teach the immune system how to make more of their own broadly neutralizing antibodies. But neutralization is not the only ability these molecules bring to the fight. The RV144 trial showed that antibodies can also battle the virus tapping other abilities that, for example, lead to the death of the infected cell. Despite these novel investigations, researchers at the conference noted that work to exploit the body’s own T cells—immune cells that can promote a response or kill an infected cell—has not been forgotten. Although vaccines based on them have thus far failed to prevent infection, they still prove somewhat effective in therapeutic applications directed at controlling viral load in those already infected. In fact, the combination of antibody and T cell approaches is one of the avenues the researchers are beginning to explore—the holy grail being a vaccine that can prevent infection as well as control virus replication. The way forward
As that work proceeds, experts are anticipating more results from follow-up studies of RV144 that should determine the effects of additional booster shots. One of the studies, RV305, showed that patients from the original RV144 trial displayed a spike in immune response with a boost six or eight years after being vaccinated. The P5 consortium is also planning to use the same vaccine structure from RV144 in South Africa, adapted to the HIV subtype common there. The future will probably also see much greater cooperation among the various camps within the field: vaccinologists and pathogenicists, preventive and therapeutic vaccines, vaccine and microbicide approaches. As a matter of fact, the Barcelona meeting was the last Aids Vaccine Conference. Next year the gathering will be called the HIV Research for Prevention Conference (H4P) and will bring together the fields of vaccines, microbicides and antiretroviral drugs. The new crossover of work and communication can only help in finding an effective vaccine, said Jose Esparza, senior advisor on global health of the Bill & Melinda Gates Foundation, during a closing plenary. It will generate even more human data, which trumps everything that is done in vitro, he said. “Different vaccine concepts need to be tested in parallel. Clinical trials are critical, especially large-scale ones,” Esparza declared. “We need to conduct our research with the necessary sense of urgency that the epidemic is imposing on us.” Follow Scientific American on Twitter @SciAm and @SciamBlogs. Visit ScientificAmerican.com for the latest in science, health and technology news.
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- HIV vaccine
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