نتایج جستجو برای: ژن il7rα
تعداد نتایج: 15796 فیلتر نتایج به سال:
A mutation in the IL7Rα locus has been identified as a risk factor for multiple sclerosis (MS), a neurodegenerative autoimmune disease characterized by inflammation, demyelination, and axonal damage. IL7Rα has well documented roles in lymphocyte development and homeostasis, but its involvement in disease is largely understudied. In this study, we use the experimental autoimmune encephalomyeliti...
Adoptive cellular therapy, in which activated tumor-reactive T cells are transferred into lymphodepleted recipients, is a promising cancer treatment option. Activation of T cells decreases IL7 responsiveness; therefore, IL15 is generally considered the main driver of effector T-cell responses in this setting. However, we found in lymphodepleted mice that CD8(+) T cells activated with IL12 showe...
The IL7Rα gene is unequivocally associated with susceptibility to multiple sclerosis (MS). Haplotype 2 (Hap 2) confers protection from MS, and T cells and dendritic cells (DCs) of Hap 2 exhibit reduced splicing of exon 6, resulting in production of relatively less soluble receptor, and potentially more response to ligand. We have previously shown in CD4 T cells that IL7Rα haplotypes 1 and 2, bu...
Newborns are unable to mount antibody responses towards certain antigens. This has been related to the restricted repertoire of immunoglobulin (Ig) genes of their B cells. The mechanisms underlying the restricted fetal Ig gene repertoire are currently unresolved. We here addressed this with detailed molecular and cellular analysis of human precursor-B cells from fetal liver, fetal bone marrow (...
In murine ontogeny, fetal liver is the major hemato- and B-lymphopoietic site until birth. Hematopoiesis develops in largely non-hematopoietic niches, which provide contacts, chemokines and cytokines that induce migration, residence, proliferation and differentiation of progenitors. Within early multipotent progenitors an IL7Rα(+)CSF-1R(+) subset expressed a mixture of lymphoid- and myeloid-spe...
BACKGROUND Allergy to peanuts results in severe anaphylactic responses in affected individuals, and has dramatic effects on society and public policy. Despite the health impacts of peanut-induced anaphylaxis (PIA), relatively little is known about immune mechanisms underlying the disease. Using a mouse model of PIA, we evaluated mice with deletions in four distinct immune molecules (IL7Rα, L-se...
سابقه و هدف: مالتیپل اسکلروزیس (ms) یک بیماری خودایمنِ همراه با تخریب میلین است. مطالعه های همبستگی ژنتیکی (gas) تأثیر مستعد کنندگیِ برخی چند شکلی های تک نوکلئوتیدی (اسنیپ) را در ژن زیر واحد آلفا گیرندۀ اینترلوکین 7 (il7ra) برای ابتلا به ms مشخص نموده است که به طور کلی مربوط به کشورهای غربی می باشد. تاکنون گزارشهای اندکی بین ژن il7ra و ms در جمعیت های آسیایی وجود دارد. اسنیپrs11567685 به دلیل...
سابقه و هدف: مالتیپلاسکلروزیس (MS) یک بیماری خودایمنِ همراه با تخریب میلین است. مطالعه های همبستگی ژنتیکی (GAS) تأثیر مستعدکنندگیِ برخی چند شکلیهای تک نوکلئوتیدی (اسنیپ) را در ژن زیر واحد آلفا گیرندۀ اینترلوکین 7 (IL7Ra) برای ابتلا به MS مشخص نموده است که به طور کلی مربوط به کشورهای غربی میباشد. تاکنون گزارشهای اندکی بین ژن IL7Ra و MS در جمعیتهای آسیایی وجود دارد. اسنیپrs11567685 به دل...
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