Details

Autor(en) / Beteiligte

• Aly, Ibrahim
• Ibrahim, Essam H
• Hamad, Rabab S
• Sayed, Hoda E L
• Attiyah, Sama M N
• E-Komy, Wafaa
• Ghramh, Hamed A
• Alshehri, Ali
• Alsyaad, Khalid M
• Alshehri, Mohammed
• Kilany, Mona
• Morsy, Kareem
• El-Kott, Attalla F
• Taha, Ramadan

Titel

The Protective Role of Toll-Like Receptor Agonist Monophosphoryl Lipid A Against Vaccinated Murine Schistosomiasis

Ist Teil von

• Acta parasitologica, 2020-09, Vol.65 (3), p.652-660

Ort / Verlag

Switzerland

Erscheinungsjahr

2020

Quelle

SpringerLink

Beschreibungen/Notizen

• Schistosomiasis is a disease that afflicts over 220 million people worldwide. To date, there is no vaccine against schistosomiasis and chemotherapy relies basically on a single drug, praziquantel. The current study was undertaken to investigate the therapeutic effects of monophosphoryl lipid A (MPLA) as an adjuvant in soluble egg antigen (SEA)-vaccinated and Schistosoma mansoni-infected mice. Mice were divided into two groups of uninfected and Schistosoma mansoni infected. The two groups were treated differently with MPLA, SEA and praziquantel. Study parameters included parasitological, immunological and biochemical parameters. Parasitological parameters revealed that intraperitoneal injection of MPLA into SEA-vaccinated and S. mansoni-infected mice was effective in reducing the worm and egg burden, granuloma count and diameter as well as the total area of infection in their livers versus SEA-untreated but infected ones. In addition, MPLA showed ameliorative action on the elevated liver oxidative stress marker, including malondialdehyde (MDA) and a decrease in the level of the antioxidant enzymes, reduced glutathione (GSH) and catalase (CAT) which may have a role in the liver damage and fibrosis due to S. mansoni infection. Treatment with MPLA has multi-functions in attenuating the deleterious impacts of S. mansoni infection in mice livers. Its effects are mediated through a reduction of ova count, worm burden, granuloma diameter and amelioration of antioxidant defense systems, and liver function biomarkers.