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Evaluation of some chemotherapeutics as anti-cryptosporidial agents in immunocompromised mice / Mennat Elrahman Ahmed Fahmy ; Supervised Amany Ahmed Abelaal , Soad Ismail Hassan , Hanaa Omar Fadl

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Mennat Elrahman Ahmed Fahmy , 2020Description: 227 P. : charts , facsimiles ; 25cmOther title:
  • تقييم بعض الأدوية كعلاج لعدوى خفيات الأبواغ فى الفئران مثبطة المناعة [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Parasitology Summary: Cryptosporidium species are apicomplexan protozoan parasites that infect gastrointestinal tract of a wide variety of animals, including humans. Since the immune status of the host is crucial for determining susceptibility to Cryptosporidium infection as well as the outcome and severity of the disease, the current work aimed to study the effect of combination therapy in treating cryptosporidiosis plus exploring the modulating effects of infection and the treatment on the local adaptive immune response in two different experimental mice models of immune-alteration; the diabetic (type 1) model and dexamethasone-treated model.The results of this study showed that the combination of selenium supplementation with ivermectin or nitazoxanide improved the percentage of oocysts reduction compared to groups receiving therapeutic drugs alone. Moreover, the combination of ivermectin with nitazoxanide gave the best oocysts reduction rates with the lowest score of ileitis severity. Immunohistochemical studies recorded the ability of treatment, in the diabetic infected groups, to up-regulate the local ileal CD4 and CD8 T cells with re-inversion of the ratio towards CD4 which is essential for cure, indicating the good impact of treatment on the local immunity. On the other hand, in all dexamethasone-treated groups, CD4 T cells were down-regulated and could not be elevated enough even after treatment. This indicates the liability of the diabetic model to tolerate Cryptosporidium infection if properly treated
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.26.Ph.D.2020.Me.E (Browse shelf(Opens below)) Not for loan 01010110082947000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.26.Ph.D.2020.Me.E (Browse shelf(Opens below)) 82947.CD Not for loan 01020110082947000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Parasitology

Cryptosporidium species are apicomplexan protozoan parasites that infect gastrointestinal tract of a wide variety of animals, including humans. Since the immune status of the host is crucial for determining susceptibility to Cryptosporidium infection as well as the outcome and severity of the disease, the current work aimed to study the effect of combination therapy in treating cryptosporidiosis plus exploring the modulating effects of infection and the treatment on the local adaptive immune response in two different experimental mice models of immune-alteration; the diabetic (type 1) model and dexamethasone-treated model.The results of this study showed that the combination of selenium supplementation with ivermectin or nitazoxanide improved the percentage of oocysts reduction compared to groups receiving therapeutic drugs alone. Moreover, the combination of ivermectin with nitazoxanide gave the best oocysts reduction rates with the lowest score of ileitis severity. Immunohistochemical studies recorded the ability of treatment, in the diabetic infected groups, to up-regulate the local ileal CD4 and CD8 T cells with re-inversion of the ratio towards CD4 which is essential for cure, indicating the good impact of treatment on the local immunity. On the other hand, in all dexamethasone-treated groups, CD4 T cells were down-regulated and could not be elevated enough even after treatment. This indicates the liability of the diabetic model to tolerate Cryptosporidium infection if properly treated

Issued also as CD

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