Association of Antibodies to Helminth Defense Molecule 1 With Inflammation, Organomegaly, and Decreased Nutritional Status in Schistosomiasis Japonica

Author:

Ruiz Amanda E12ORCID,Pond-Tor Sunthorn1,Stuart Ronald1,Acosta Luz P3,Coutinho Hannah M3,Leenstra Tjalling34,Fisher Sydney1,Fahey Owen1,McDonald Emily A14,Jiz Mario A123,Olveda Remigio M1,McGarvey Stephen T5,Friedman Jennifer F14,Wu Hannah Wei14,Kurtis Jonathan D12

Affiliation:

1. Center for International Health Research, Rhode Island Hospital, Brown University Medical School , Providence, Rhode Island , USA

2. Department of Pathology and Laboratory Medicine, Brown University Medical School , Providence, Rhode Island , USA

3. Department of Immunology, Research Institute of Tropical Medicine , Manila , the Philippines

4. Department of Pediatrics, Rhode Island Hospital, Brown University Medical School , Providence, Rhode Island , USA

5. Department of Epidemiology and International Health Institute, Brown University School of Public Health , Providence, Rhode Island , USA

Abstract

Abstract Immunomodulation enhances parasite fitness by reducing inflammation-induced morbidity in the mammalian host, as well as by attenuating parasite-targeting immune responses. Using a whole-proteome differential screening method, we identified Schistosoma japonicum helminth defense molecule 1 (SjHDM-1) as a target of antibodies expressed by S. japonicum–resistant but not S. japonicum–susceptible individuals. In a longitudinal cohort study (n = 644) conducted in a S. japonicum–endemic region of the Philippines, antibody levels to SjHDM-1 did not predict resistance to reinfection but were associated with increased measures of inflammation. Individuals with high levels of anti–SjHDM-1 immunoglobulin G had higher levels of C-reactive protein than those with low anti–SjHDM-1. High anti–SjHDM-1 immunoglobulin G responses were also associated with reduced biomarkers of nutritional status (albumin), as well as decreased anthropometric measures of nutritional status (weight-for-age and height-for-age z scores) and increased measures of hepatomegaly. Our results suggest that anti–SjHDM-1 responses inhibit the immunomodulatory function of SjHDM-1, resulting in increased morbidity rates.

Funder

Howard Hughes Medical Institute

Brown University Initiative to Maximize Student Development Program

National Institute of General Medical Sciences

National Institutes of Health

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

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