Gender-dependent specific immune response during chronic human Schistosomiasis haematobia

Author:

Remoué F1,To Van D2,Schacht A-M1,Picquet M3,Garraud O4,Vercruysse J3,Ly A2,Capron A1,Riveau G1

Affiliation:

1. INSERM Unité 167, Institut Pasteur de Lille, Lille, France

2. Programme ESPOIR, 
Région Médicale de St-Louis, Saint-Louis, Sénégal

3. Laboratory of Parasitology, University of Gent, Merelbeke, Belgium and

4. Unité d’Immunologie, Institut Pasteur de Dakar, Dakar, Sénégal

Abstract

SUMMARY The cellular and humoral acquired immune responses to Schistosoma haematobium 28 kD gluthathione S-Transferase (Sh28GST) antigen were evaluated in a Senegalese population chronically infected with S. haematobium parasite. We show a gender-dependent immune response in adult individuals presenting similar intensities of infection. Indeed, the specific IgA response and production of TGF-β and IL-10 were found significantly higher in females compared to males. In addition, we showed that this profile was combined with a weak production of Th1-related cytokines (TNFα and IFNγ) and was associated with an absence of proliferation to the antigen. A significantly higher Nuclear Matrix Protein 41/7 secretion, an apoptosis marker, was specifically observed in mononuclear blood cell cultures of females suggesting that a specific cell death process was engaged in a gender-dependent manner. This specific profile could be associated with the so-called T helper type-3 (Th3) immune response specifically promoting the production of IgA and would be developed upon the down-regulation of the specific Type-1 response by a probable cell death mechanism. This gender-dependent immune regulation, which may be under the influence of nonimmunological factors like sexual hormones, may be related to the chronicity of the infection.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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