Dr Deborah Burnett
Media Release: 25 August 2020
Researchers at the Garvan Institute of Medical Research have uncovered a key strategy the immune system uses to generate effective antibodies, which could inform vaccine design for some of the most challenging viruses.
In experimental models, the researchers discovered that the immune system mutated its B cells to generate more finely-tuned antibodies when the targets for those antibodies, referred to as ‘antigens’, were structurally flexible, rather than rigid. The researchers publish their findings in the journal PNAS.
“Our findings address a central issue for developing vaccines – how the immune system generates antibodies that recognise ‘foreign’ from ‘self’,” says co-senior author Professor Daniel Christ, Head of Antibody Therapeutics and Director of the Centre of Targeted Therapy at Garvan.
“Taking a comprehensive analytical approach, we found that a flexible target allows the immune system to create antibodies more finely-tuned to foreign molecules, which we hope will play a role in informing the design of future vaccines.”
Our immune system is constantly challenged by foreign microbes such as viruses. To clear a virus from our body, and to remember and eliminate it more quickly the next time we’re exposed, our immune system evolves. This happens in structures called germinal centres within our lymph nodes, where B cells multiply and mutate to produce antibodies more finely-tuned to target the virus.
“Long-lasting immunity is an important challenge for the immune system – antibodies have to bind like glue to foreign threats, such as viruses but avoid any of the body’s own molecules as this can lead to autoimmunity,” says Dr Deborah Burnett, co-first author of the paper.
At a sub-microscopic level, some molecules bend and move more than others – some are more rigid, while others are flexible. The same is true for molecules on viruses, for example, the spike protein on the SARS-CoV-2 virus that causes COVID-19 is highly flexible to adopt multiple different shapes.
“There is a longstanding debate about whether flexible or rigid antigens in vaccines are more likely to elicit a lasting immune response in humans. We wanted to help answer that question,” says Dr Peter Schofield, co-first author of the study.
More paths to reach fine-tuned immunity
“Using an artificial pair of foreign and self-molecules that are very similar, we created different versions of the same antigen, altering one connection that made it either more rigid or more flexible,” says Dr Schofield. The researchers then investigated how the immune system of mice generated antibodies to the different molecules.
The researchers discovered that when the foreign antigen was more flexible, the germinal centre could employ a greater number of evolution strategies to make antibodies that bound foreign but not self-molecules.
“Our results showed that the antibodies initially bonded to both the rigid self and flexible foreign antigens in the same way, unable to tell them apart. What surprised us was that, after only a few weeks, when the foreign antigen was flexible, the antibodies were able to specifically mutate to become 67 times more selective for foreign antigens, and 19 times less selective for self,” says Dr Burnett. “The antibodies generated against rigid foreign antigens were more likely to have autoimmune properties.”
Informing vaccine design
The ability to produce antibodies that bind foreign but not self-molecules is a major hurdle for vaccine development, say the researchers.
“It’s the major roadblock in the generation of effective HIV vaccines, which have so far been blocked by checkpoints in the body that avoid an autoimmune response,” says Professor Chris Goodnow, Garvan’s Executive Director and co-senior author of the study. “What we have discovered is fundamental to establishing long-lived immunity, which will inform vaccine design going forward.”
“There is circumstantial evidence that antibodies against the spike molecule on the SARS-CoV-2 virus may also recognise ‘self’. This may be an explanation for why antibody levels against the novel coronavirus appear to decline in patients quickly after infection,” he adds. “Understanding how to increase selection of antibodies that don’t bind self may illuminate a pathway to long-lived immunity against COVID-19.”
This research was supported by Australia’s National Health and Medical Research Council (Program Grants 1016953 & 1113904, Project Grant 1108800, and Fellowships 585490, 1157744, 190774, 1176351 & 1081858), the Australian Research Council (Discovery Grants 160104915 & 140103465) and the Bill and Patricia Ritchie Family Foundation.
Dr Viviane Richter
Garvan Institute of Medical Research