Antibody fucosylation predicts disease severity in secondary dengue infection

Author:

Bournazos Stylianos1ORCID,Vo Hoa Thi My2ORCID,Duong Veasna3ORCID,Auerswald Heidi3ORCID,Ly Sowath4ORCID,Sakuntabhai Anavaj56ORCID,Dussart Philippe3ORCID,Cantaert Tineke2ORCID,Ravetch Jeffrey V.1ORCID

Affiliation:

1. Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY, USA.

2. Immunology Unit, Institut Pasteur du Cambodge, Institut Pasteur International Network, Phnom Penh, Cambodia.

3. Virology Unit, Institut Pasteur du Cambodge, Institut Pasteur International Network, Phnom Penh, Cambodia.

4. Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Institut Pasteur International Network, Phnom Penh, Cambodia.

5. Functional Genetics of Infectious Diseases Unit, Department of Global Health, Institut Pasteur, Paris Cedex 15, France.

6. Centre National de la Recherche Scientifique (CNRS), UMR2000, Paris Cedex 15, France.

Abstract

IgG fucosylation predicts dengue severity Secondary infections with dengue virus (DENV) can produce life-threatening symptoms, including thrombocytopenia and hemorrhagic disease, when preexisting DENV-reactive immunoglobulin G1 (IgG1) antibodies promote the infection of immune cells. Although severe dengue symptoms are associated with increased levels of afucosylated IgG1 glycoforms, it is unclear whether this is simply a result of the infection or if it is a preexisting phenomenon that can dictate susceptibility to this disease. Bournazos et al. studied the Fab and Fc structures of anti-DENV antibodies from patients before and after infection and with variable disease outcomes (see the Perspective by de Alwis and Ooi). They found that DENV infection induced specific increases in IgG1 afucosylation, and levels of afucosylated IgG1 could indeed predict dengue disease severity, making IgG1 fucosylation status a potentially useful prognostic tool for the treatment of dengue patients. Science , abc7303, this issue p. 1102 ; see also abj0435, p. 1041

Funder

National Heart, Lung, and Blood Institute

National Institute of Allergy and Infectious Diseases

European Union Seventh Framework Program

Department of Health and Human Services

Howard Hughes Medical Institute/Wellcome Trust

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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