Polyreactive antibodies as potential humoral biomarkers of host resistance to cystic echinococcosis. (5th November 2020)

• Record Type: Journal Article
• Authors: García‐Luna, Joaquín; Magnone, Javier; Miles, Sebastián; López‐Santurio, Camila; Dematteis, Sylvia; Mourglia‐Ettlin, Gustavo
• Is Part Of: Parasite immunology. Volume 43:Number 3(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-11-05
• Subjects: biomarkers -- cystic echinococcosis -- Echinococcus granulosus -- polyreactive antibodies -- resistance; Veterinary parasitology -- Immunological aspects -- Periodicals; Host-parasite relationships -- Immunological aspects -- Periodicals; 571.96
• DOI: 10.1111/pim.12802
• Languages: English
• ISSNs: 0141-9838

Abstract

Abstract: Polyreactive antibodies (pAb) bind to a broad range of unrelated structures, providing hosts with functional components able to rapidly recognize and protect against different pathogens. However, their roles against helminth parasites are still unexplored. Here, pAb profiles were analysed in cystic echinococcosis (CE), a zoonosis caused by the cestode Echinococcus granulosus sensu lato . Levels of anti‐DNP (2, 4‐dinitrophenyl‐hapten) antibodies were measured as a surrogate parameter of pAb in different biological settings. Firstly, levels of serum and peritoneal pAb were measured during early experimental secondary CE, using both high (Balb/c) and low (C57Bl/6) susceptible mouse strains. Serum pAb mostly differed in normal mice, being pAb levels of IgG subclasses with poor anti‐parasite activities predominant in Balb/c animals. Conversely, peritoneal pAb isotypes/subclasses with efficient anti‐parasite activities predominated in normal and infected C57Bl/6 mice. Secondly, sera from potentially resistant patients, susceptible individuals and healthy donors were analysed, showing higher pAb levels of the IgA and IgG—particularly IgG1—isotypes in potentially resistant individuals compared to control groups. Finally, since remarkable differences were observed in pAb profiles according to the intrinsic host susceptibility to the infection, we proposed here that pAb might be considered as potential humoral biomarkers for host resistance to CE.