A broadly protective antibody that targets the flavivirus NS1 protein

Author:

Modhiran Naphak1ORCID,Song Hao23ORCID,Liu Lidong4,Bletchly Cheryl5,Brillault Lou16,Amarilla Alberto A.1ORCID,Xu Xiaoying2,Qi Jianxun2ORCID,Chai Yan2ORCID,Cheung Stacey T. M.1,Traves Renee1ORCID,Setoh Yin Xiang1ORCID,Bibby Summa1,Scott Connor A. P.1ORCID,Freney Morgan E.1ORCID,Newton Natalee D.1ORCID,Khromykh Alexander A.1,Chappell Keith J.1ORCID,Muller David A.1ORCID,Stacey Katryn J.1ORCID,Landsberg Michael J.1ORCID,Shi Yi2ORCID,Gao George F.23ORCID,Young Paul R.1ORCID,Watterson Daniel1ORCID

Affiliation:

1. Australian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Australia.

2. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.

3. Research Network of Immunity and Health (RNIH), Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.

4. Division of Laboratory Medicine, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

5. Microbiology, Pathology Queensland, Queensland Health, Herston, Queensland, Australia.

6. Centre for Microscopy and Microanalysis, The University of Queensland, Brisbane, Australia.

Abstract

Two antibodies against flaviviruses Flaviviruses are a group of RNA viruses that include the human pathogens dengue virus, Zika virus, and West Nile virus. The envelope protein (E) on the virus surface has been the target of vaccine development, but problems have arisen with antibodies against E, leading to enhanced infection. Now, Modhiran et al. and Biering et al. describe two different antibodies that bind to the flavivirus NS1 protein and prevent it from disrupting epithelial cells, which is associated with severe disease. Both antibodies cross-react with multiple flavivirus NS1 proteins. The antibodies reduce viremia and increase survival in mouse models of flavivirus disease. Both papers include structures of NS1 bound to an antibody, which give insight into the protective mechanism. Science , this issue p. 190 , p. 194

Funder

National Health and Medical Research Council

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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