CD71 targeting boosts immunogenicity of sublingually delivered influenza haemagglutinin antigen and protects against viral challenge in mice
Vaccines are complicated. The research and development, the
pricing, the delivery (getting them to the right people), the acceptance
(getting the right people to take them) are all complicated. Vaccines are
unlike other forms of medicine because they are universally prescribed as a
preventative rather than a cure. When vaccines are successful, they can be
self-defeating because they reduce the disease and therefore the fear of the
disease, which gets people to use them in the first place.
Vaccine uptake varies for various sensible and less sensible
reasons, which you can track live at the vaccine confidence project run by
the London school of hygiene and tropical medicine. One reason for poor vaccine
uptake is fear of needles and therefore one approach to improve vaccines is to
develop vaccines that don’t need needles.
Going needle free
Finding alternatives to needles is more than a ‘first world
problem’. There has been, historically, an issue with the re-use of dirty
needles and the spread of blood borne diseases. This has been reduced by moving
to syringes that can only be used once. Vaccines without needles may also be
scientifically better. Delivering vaccine to the site of infection (or mucosal
delivery) can improve the response to the vaccine. The mucosa refers to
internal body surfaces that face the outside (and have mucus): it includes the
nose and lungs, mouth, stomach and guts and genital tract. These tissues are a
major route into the body for a wide range of infectious organisms, so require
extra vigilant immunity. But, critically, mucosal surfaces are sites of
exchange (lungs – oxygen, guts – food, genitals – babies). They therefore need
to be porous enough to allow in beneficial material but not so porous that bugs
can get in. Balancing these two needs leads to specialised immune responses at
mucosal surfaces. In our
current study: “CD71 targeting boosts immunogenicity of sublingually
delivered influenza haemagglutinin antigen and protects against viral challenge
in mice”, we exploited our knowledge of mucosal immunology to develop better
vaccines.
On the tip of your tongue
Paul and Jamie (co-authors on the paper) have previously
shown that targeting a specific molecule called the transferrin receptor
(whose normal purpose is to pump iron into the body, also known as CD71) can improve
the quality of vaccine responses. It has been shown that applying vaccines
under the tongue (sublingually) can lead to a better response. The current
study looked at combining these two approaches – targeting the transferrin
receptor on the tongue to deliver vaccines. When used, the immune response to
influenza was significantly improved, leading to a more protective vaccine.
This approach could be used for a range of diseases, removing needles and
improving the response.
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