Whole-Proteome Differential Screening Identifies Novel Vaccine Candidates for Schistosomiasis japonica

Author:

Wu Hannah W12ORCID,Park Sangshin123,Pond-Tor Sunthorn1,Stuart Ron1,Zhou Sha14,Hong Yang15,Ruiz Amanda E1,Acosta Luz16,Jarilla Blanca6,Friedman Jennifer F12,Jiz Mario6,Kurtis Jonathan D17

Affiliation:

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

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

3. Graduate School of Urban Public Health, University of Seoul, Seoul, Republic of Korea

4. Department of Pathogen Biology, Key Laboratory of Pathogen Biology of Jiangsu Province, Nanjing Medical University, Nanjing, China

5. Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Animal Parasitology, Ministry of Agriculture of China, Shanghai, China

6. Department of Immunology, Research Institute of Tropical Medicine, Manila, Philippines

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

Abstract

Abstract Schistosomiasis remains a leading cause of chronic morbidity in endemic regions despite decades of widespread mass chemotherapy with praziquantel. Using our whole proteome differential screening approach, and plasma and epidemiologic data from a longitudinal cohort of individuals living in a Schistosoma japonicum–endemic region of the Philippines, we interrogated the parasite proteome to identify novel vaccine candidates for Schistosoma japonicum. We identified 16 parasite genes which encoded proteins that were recognized by immunoglobulin G or immunoglobulin E antibodies in the plasma of individuals who had developed resistance to reinfection, but were not recognized by antibodies in the plasma of individuals who remained susceptible to reinfection. Antibody levels to Sj6-8 and Sj4-1 measured in the entire cohort (N = 505) 1 month after praziquantel treatment were associated with significantly decreased risk of reinfection and lower intensity of reinfection over 18 months of follow-up.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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