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رسائل دكتوراة الانجليزية 2014 08f37a65-0074-4c77-9fd3-9aecc0bc68b4

ROLE OF MYD88 PROTEIN IN THE MAINTENANCE OF IMMUNOLOGICAL SELF-TOLERANCE: INDUCTION OF AUTOIMMUNITY BY SALMONELLA INFECTION CONSEQUENT TO MYD88 DEFICIENCY

Jincy Merin Issac, باسل الرمادي

كلية الطب والعلوم الصحية-جامعة الإمارات العربية المتحدة · الامارات

الموضوعات

طب

الملخص

Activation of the innate immune system is a prerequisite for the induction of adaptive immune responses to both infectious and non-infectious agents. Toll-like receptors (TLRs) are a family of proteins important for recognizing pathogen associated molecular patterns. MyD88 is an adaptor molecule whose function is critical in TLR signaling. MyD88-deficient (MyD88-/-) mice exhibit heightened susceptibility to infections, even by attenuated strains of Salmonella enterica serovar Typhimurium. Paradoxically, despite their hypersusceptibility, infected MyD88-/- mice produce elevated serum levels of anti-Salmonella antibodies regardless of the route of infection. This hypergammaglobulinemia was observed with both Th1-driven (IgG2c and IgG3) and Th2-driven (IgG1) antibody isotypes. The dysregulated antibody responses also led to the production of autoantibodies as demonstrated by reactivity to dsDNA and thyroglobulin, positive nuclear staining with HEp2 cells, and immune complex deposition in the kidneys of MyD88-/- mice. Utilizing intracellular cytokine staining, real-time PCR and 6-color flowcytometric analysis, we demonstrated that these autoimmune responses correlate with the activation of distinct populations of IFN-+/IL-4+ and IFN+/IL-10+ T helper lymphocytes. Further analysis revealed that these most likely represent a specialized family of cells known as follicular helper T cells (TFH cells) which function to promote B cell activation and antibody production. The aberrant expansion of these TFH-like cells could underlie the activation of autoreactive B cells leading to humoral autoimmunity. Our findings highlight a critical role for TLR-MyD88 pathway in controlling reactivity to self-antigens and provide a potential mechanism for the inter-relationship between microbial infections and autoimmune disease development in humans.

التعريف والنوع

رقم الوثيقة
08f37a65-0074-4c77-9fd3-9aecc0bc68b4
رقم العقد
0
نوع الوسائط
Crawler
نوع المحتوى
الرسائل العلمية
صيغة المصدر
رسائل دكتوراة
نوع الملف
pdf text
أسماء الملفات
7142_1.pdf

بيانات النشر

ألقاب المؤلفين
[{"name_ar":"Jincy Merin Issac","title_ar":"اعداد","title_en":"Preparation"},{"name_ar":"باسل الرمادي ","title_ar":"اشراف","title_en":"Supervision"}]
اللغة
English

المصدر والدورية

اسم المصدر
ROLE OF MYD88 PROTEIN IN THE MAINTENANCE OF IMMUNOLOGICAL SELF-TOLERANCE: INDUCTION OF AUTOIMMUNITY BY SALMONELLA INFECTION CONSEQUENT TO MYD88 DEFICIENCY

المحتوى والصفحات

عدد الصفحات
0

إشراف وإعداد

الإشراف
باسل الرمادي
الإعداد
Jincy Merin Issac

الاقتباسات الببليوغرافية

APA

Jincy Merin Issac و باسل الرمادي . (2014). ROLE OF MYD88 PROTEIN IN THE MAINTENANCE OF IMMUNOLOGICAL SELF-TOLERANCE: INDUCTION OF AUTOIMMUNITY BY SALMONELLA INFECTION CONSEQUENT TO MYD88 DEFICIENCY. أطروحة(رسائل دكتوراة). كلية الطب والعلوم الصحية-جامعة الإمارات العربية المتحدة. الامارات .

MLA

Jincy Merin Issac و باسل الرمادي . ROLE OF MYD88 PROTEIN IN THE MAINTENANCE OF IMMUNOLOGICAL SELF-TOLERANCE: INDUCTION OF AUTOIMMUNITY BY SALMONELLA INFECTION CONSEQUENT TO MYD88 DEFICIENCY. 2014. كلية الطب والعلوم الصحية-جامعة الإمارات العربية المتحدة، رسائل دكتوراة.