Background Hydatid disease is a widespread disease that affects all human organs. Aims This study aimed to evaluate antibodies (IgA, IgG, and IgM), complement proteins (C3 and C4), MIF of PMNs cells, reduction of nitro blue tetrazolium (NBT), and phagocytic activity against Candida albicans. Methodology Hydatid cysts were collected from surgically injured patients at Fallujah Teaching Hospital, Twenty BALB/c mice were injected with Protoscolex antigen as treatment groups or phosphate-buffered saline (PBS) as control groups, at booster and challenge doses. Antibodies and complement concentrations were measured by enzyme-linked immunosorbent assay (ELISA), and the MIF of PMNs cells, reduction of NBT, and phagocytic activity against Candida albicans were measured to assess cellular activity. Results The results showed significant differences in the levels of antibodies compared to the control group 21 days after injection of the protoscolex antigen at a concentration of 0.5 ml subcutaneously. There were also significant differences between the treatment and control group in the levels of C3 and C4. NBT dye reduction and phagocytosis of Candida albicans by PMNs showed significant differences compared to the control group. The results also showed a significant decrease in PMN viability in the treatment group. An increase in neutrophil migration diameter was observed. The results showed a 50.4% decrease in the infection level in the treatments injected with the antigen, and the average diameter of the hydatid cysts decreased compared with the control group. Conclusions The results indicate that Protoscolex antigen activates the immune response and reduces severity of hydatid disease. This highlights its potential as a promising candidate for developing a vaccine or preventive strategy against hydatid disease.
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Amir Hussain
Edinburgh Napier University
Anwar Khalil Ismael
Mohammed Y. I. Al-Hamadani
University Of Fallujah
F1000Research
University Of Fallujah
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Hussain et al. (Thu,) studied this question.
synapsesocial.com/papers/69a75c5dc6e9836116a25303 — DOI: https://doi.org/10.12688/f1000research.174636.1