Animal tests suggest inhaled COVID-19 vaccine may prevent disease

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Chinese and Australian scientists have developed an inhaled COVID-19 vaccine, and tests in animals found it triggers an immune response and confers strong protection against infection. The researchers hope their new vaccine, which is based on a modified bacterial protein, will be more effective than injected vaccines at preventing infection because it primes the airways, which injectable liquid vaccines do not. They say their vaccine should also be simpler and cheaper to transport as it's a dry powder that doesn't require cold storage to remain stable.

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From: Springer Nature

Development of an inhaled vaccine for COVID-19 

The development of an inhaled vaccine for SARS-CoV-2 is reported in Nature. The compound elicits an increased immune response compared to pre-vaccination and confers strong protection against infection in mice, hamsters, and nonhuman primates, showing promise as an alternative to injections.

Since it was declared a pandemic in early 2020, numerous efforts have been made to develop and approve vaccines for COVID-19. The majority of successful candidates are delivered via intramuscular injections, which induce the production of the antibody immunoglobulin G (IgG). These have proved effective at preventing severe disease, however, they have limited efficacy for preventing infection, as this requires inducing immunity within the mucosal tissue in the lungs and airways. In addition, they are often in liquid form, which necessitates cold chain storage conditions to keep them stable, resulting in increased costs.

Guanghui Ma and colleagues developed an inhalable, dry powder aerosol vaccine for SARS-CoV-2. The vaccine encapsulates a non-toxic bacterial protein called CTB, which is modified to display the SARS-CoV-2 receptor-binding domain antigen, within microcapsules small enough to enter and deposit deep within the lungs. Additionally, a ‘mosaic iteration’ of the vaccine was produced, which contained both ancestral and Omicron variant viruses, to test efficacy against fighting multiple strains.

Following a single dose, the candidate was delivered efficiently to mucosal tissue within the lungs and showed sustained antigen release and successful uptake by antigen-presenting cells. It also induced a long-term increase in IgG and immunoglobulin A (IgA) production in mice, hamsters, and nonhuman primates, which provides effective protection against SARS-CoV-2 infection. The ‘mosaic iteration’ of the vaccine was associated with extending the breadth of this antibody response in both serum and mucus samples, suggesting an effectiveness at tackling co-circulating strains and the Omicron variant. Additionally, the powder was shown to be stable at room temperature after one month of storage, which could reduce the storage and transportation costs of distributing the vaccine, therefore making it more accessible.

This inhaled vaccine shows promise as a way to prevent COVID-19 by targeting the lung cells directly, inducing a more robust immune response than previous inhaled vaccines. The aerosol delivery system has potential as a tool to combat both COVID-19 and other respiratory diseases, the authors conclude. 

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conference:
Nature
Research:Paper
Organisation/s: The University of Queensland, Chinese Academy of Sciences, China, McMaster University, Canada
Funder: This work was supported by the National Natural Science Foundation of China (grant nos. T2225021, 21821005, 32030062, U2001224, 81930122, U20A20361 and 82202028), Beijing Natural Science Foundation (JQ21027), CAS Project for Young Scientists in Basic Research (YSBR-083), National Key Research and Development Program of China (2021YFC2302600), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB29040303), CAMS Innovation Fund for Medical Science (2021-I2M-1-024), and the Major Science and Technology Special Projects of Yunnan Province (202002AA100009). We thank X. Zhao for providing wild-type and Omicron pseudotyped viruses and B. Wang for providing the SARS-CoV-2 RBD peptide pool.
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