Your browser doesn't support javascript.
loading
Deep humoral profiling coupled to interpretable machine learning unveils diagnostic markers and pathophysiology of schistosomiasis.
Saha, Anushka; Chakraborty, Trirupa; Rahimikollu, Javad; Xiao, Hanxi; de Oliveira, Lorena B Pereira; Hand, Timothy W; Handali, Sukwan; Secor, W Evan; A O Fraga, Lucia; Fairley, Jessica K; Das, Jishnu; Sarkar, Aniruddh.
Afiliación
  • Saha A; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30309, USA.
  • Chakraborty T; Center for Systems Immunology, Departments of Immunology and Computational & Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Rahimikollu J; Integrative Systems Biology Program, Pittsburgh, PA 15213, USA.
  • Xiao H; Center for Systems Immunology, Departments of Immunology and Computational & Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • de Oliveira LBP; Joint CMU-Pitt Ph.D. Program in Computational Biology, Pittsburgh, PA 15213, USA.
  • Hand TW; Center for Systems Immunology, Departments of Immunology and Computational & Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Handali S; Joint CMU-Pitt Ph.D. Program in Computational Biology, Pittsburgh, PA 15213, USA.
  • Secor WE; Programa Multicêntrico de Bioquímica e Biologia Molecular (PMBqBM), Federal University of Juiz de Fora, Campus Governador Valadares, Juiz de Fora, Minas Gerais 36036-900, Brazil.
  • A O Fraga L; University Vale do Rio Doce, Governador Valadares, Minas Gerais 36036-900, Brazil.
  • Fairley JK; Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Das J; Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
  • Sarkar A; Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Sci Transl Med ; 16(765): eadk7832, 2024 Sep 18.
Article en En | MEDLINE | ID: mdl-39292803
ABSTRACT
Schistosomiasis, a highly prevalent parasitic disease, affects more than 200 million people worldwide. Current diagnostics based on parasite egg detection in stool detect infection only at a late stage, and current antibody-based tests cannot distinguish past from current infection. Here, we developed and used a multiplexed antibody profiling platform to obtain a comprehensive repertoire of antihelminth humoral profiles including isotype, subclass, Fc receptor (FcR) binding, and glycosylation profiles of antigen-specific antibodies. Using Essential Regression (ER) and SLIDE, interpretable machine learning methods, we identified latent factors (context-specific groups) that move beyond biomarkers and provide insights into the pathophysiology of different stages of schistosome infection. By comparing profiles of infected and healthy individuals, we identified modules with unique humoral signatures of active disease, including hallmark signatures of parasitic infection such as elevated immunoglobulin G4 (IgG4). However, we also captured previously uncharacterized humoral responses including elevated FcR binding and specific antibody glycoforms in patients with active infection, helping distinguish them from those without active infection but with equivalent antibody titers. This signature was validated in an independent cohort. Our approach also uncovered two distinct endotypes, nonpatent infection and prior infection, in those who were not actively infected. Higher amounts of IgG1 and FcR1/FcR3A binding were also found to be likely protective of the transition from nonpatent to active infection. Overall, we unveiled markers for antibody-based diagnostics and latent factors underlying the pathogenesis of schistosome infection. Our results suggest that selective antigen targeting could be useful in early detection, thus controlling infection severity.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquistosomiasis / Biomarcadores / Aprendizaje Automático Límite: Adult / Animals / Female / Humans Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquistosomiasis / Biomarcadores / Aprendizaje Automático Límite: Adult / Animals / Female / Humans Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos