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The effect of treatment with mesenchymal stem cells on mice treated with collagen induced arthritis : Possible role of interleukin 4 / Shaimaa Moustafa Haikal ; Supervised Magdy Ali Amin , Laila Ahmed Rashed , Nourtan F. Abdeltawab

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Shaimaa Moustafa Haikal , 2016Description: 83 P. : photographs ; 25cmOther title:
  • تأثير العلاج بالخلايا الجذعية الوسيطة على الفئران المعالجه بالكولاجين المسبب لمرض التهاب المفاصل : الدور المحتمل للانترليوكين4 [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Microbiology and Immunology Summary: Rheumatoid arthritis (RA) is a debilitating disease causing decreased quality of life. The disease affects primarily small joints of the hands and feet and is classified as a chronic autoimmune disorder. Mesenchymal stromal cells (MSCs) have been shown to exert immunosuppressive activity with the possibility for use in the treatment of RA. Similarly, interleukin (IL)-4 has been investigated as a possible RA treatment. Therefore, in the current study, we aimed to investigate the effect of combination therapy of bone marrow-derived MSCs (BM-MSCs) and IL-4 as a possible treatment of murine collagen-induced arthritis (CIA). We induced arthritis in Balb/c mice by intradermal injection of 100 æg of type II collagen (CII) at day 0 and 21 and mice were examined daily for the onset of clinical manifestations of arthritis. Mice were divided into four groups, first group received intravenous injection (i.v.) of MSCs only, second group received intraperitoneal injection (i.p.) of IL-4 only, and a third group received i.v. and i.p MSCs and IL-4 respectively. A fourth CIA control group received PBS after induction of arthritis. In addition, a fifth group of untreated mice served as healthy controls. After four weeks of treatment, we collected blood from each group and mice were sacrificed and synovial tissue was examined. RA was evident in CIA control group by histopathological examination of knee joints that showed erosions of articular cartilage, edema and influx of inflammation compared to healthy controls
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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 Cai01.08.06.M.Sc.2016.Sh.E (Browse shelf(Opens below)) Not for loan 01010110071133000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.06.M.Sc.2016.Sh.E (Browse shelf(Opens below)) 71133.CD Not for loan 01020110071133000

Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Microbiology and Immunology

Rheumatoid arthritis (RA) is a debilitating disease causing decreased quality of life. The disease affects primarily small joints of the hands and feet and is classified as a chronic autoimmune disorder. Mesenchymal stromal cells (MSCs) have been shown to exert immunosuppressive activity with the possibility for use in the treatment of RA. Similarly, interleukin (IL)-4 has been investigated as a possible RA treatment. Therefore, in the current study, we aimed to investigate the effect of combination therapy of bone marrow-derived MSCs (BM-MSCs) and IL-4 as a possible treatment of murine collagen-induced arthritis (CIA). We induced arthritis in Balb/c mice by intradermal injection of 100 æg of type II collagen (CII) at day 0 and 21 and mice were examined daily for the onset of clinical manifestations of arthritis. Mice were divided into four groups, first group received intravenous injection (i.v.) of MSCs only, second group received intraperitoneal injection (i.p.) of IL-4 only, and a third group received i.v. and i.p MSCs and IL-4 respectively. A fourth CIA control group received PBS after induction of arthritis. In addition, a fifth group of untreated mice served as healthy controls. After four weeks of treatment, we collected blood from each group and mice were sacrificed and synovial tissue was examined. RA was evident in CIA control group by histopathological examination of knee joints that showed erosions of articular cartilage, edema and influx of inflammation compared to healthy controls

Issued also as CD

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