نتایج جستجو برای: cd40 ligand cd154

تعداد نتایج: 111671  

Journal: :The Egyptian journal of immunology 2009
Ola A Hussein Alaa A Omran Amina M Elnaggar Ayman Fathy

Chronic lymphocytic leukemia (CLL) is a haematopoetic neoplasm caused primarily by defects in apoptosis mechanisms and complicated by progressive marrow failure, immunosupression and increased resistance to chemotherapy. The CD40-CD40 ligand (CD40L) interaction has been shown to significantly increase antigen presentation in normal and malignant B-cells and it is a powerful regulator of cell su...

Journal: :International immunology 2001
L L Pearson B E Castle M R Kehry

The biochemical pathways involved in CD40 signaling have been extensively studied in B cells and B cell lines, and appear to be primarily initiated by recruitment of the tumor necrosis factor (TNF) receptor-associated factor (TRAF) signaling proteins to the CD40 cytoplasmic domain. Signaling pathways activated through CD40 in monocytes/macrophages have not been characterized as well as in B cel...

Journal: :Infection and immunity 2001
A R Hayward M Cosyns M Jones E M Ponnuraj

To clear a Cryptosporidium parvum infection, mice need CD4+ T cells, major histocompatibility complex class II, and an intact CD40-CD154 signaling pathway. CD40 is constitutively expressed on marrow-derived cells such as dendritic cells and B lymphocytes and is induced by gamma interferon (IFN-gamma) on most somatic cells. To determine whether the CD40 needed to clear a C. parvum infection has ...

Journal: :Blood 2005
Lan V Pham Archito T Tamayo Linda C Yoshimura Yen-Chiu Lin-Lee Richard J Ford

Abnormalities in B-lymphocyte CD40 ligand (CD154) expression have been described for a number of immunologic diseases, including B-cell lymphomas. Although functional analysis of the CD154 gene and protein has been extensive, little is known about the mechanisms controlling CD154 expression in activated T cells, and even less is known for normal and malignant B cells. In this study we describe ...

2012
Ivana R. Ferrer Maylene E. Wagener Mingqing Song Mandy L. Ford

CD154/CD40 blockade combined with donor specific transfusion remains one of the most effective therapies in prolonging allograft survival. Despite this, the mechanisms by which these pathways synergize to prevent rejection are not completely understood. Utilizing a BALB/c (H2-K(d)) to B6 (H2-K(b)) fully allogeneic skin transplant model system, we performed a detailed longitudinal analysis of th...

Journal: :Journal of immunology 2012
Ivana R Ferrer Danya Liu David F Pinelli Brent H Koehn Linda L Stempora Mandy L Ford

Blockade of the CD40/CD154 pathway remains one of the most effective means of promoting graft survival following transplantation. However, the effects of CD40/CD154 antagonism on dendritic cell (DC) phenotype and functionality following transplantation remain incompletely understood. To dissect the effects of CD154/CD40 blockade on DC activation in vivo, we generated hematopoietic chimeras in m...

Journal: :Cancer research 1999
F Sbih-Lammali B Clausse H Ardila-Osorio R Guerry M Talbot S Havouis L Ferradini J Bosq T Tursz P Busson

The expression and function of CD95 and CD40 were investigated in malignant cells from EBV-positive undifferentiated nasopharyngeal carcinomas (NPCs). Large amounts of CD95 and CD40 expression were detected in 15 of 16 EBV-positive NPC specimens. In contrast, CD95 was not detected in two biopsies from patients with EBV-negative differentiated NPCs. We tested whether the CD95 apoptotic pathway w...

Journal: :Journal of immunology 2006
Basel K al-Ramadi Maria J Fernandez-Cabezudo Azim Ullah Hussain El-Hasasna Richard A Flavell

CD40-CD154 interactions are of central importance in the induction of humoral and cellular immune responses. In the present study, CD154-deficient (CD154-/-) mice were used to assess the role of CD40-CD154 interactions in regulating the immune response to a systemic Salmonella infection. Compared with C57BL/6 (CD154+/+) controls, CD154-/- mice were hypersusceptible to infection by an attenuated...

Journal: :Journal of immunology 2009
Ilia N Buhtoiarov Alexander L Rakhmilevich Lewis L Lanier Erik A Ranheim Paul M Sondel

Under different circumstances, tumors can inhibit or activate macrophage (Mphi) effector functions. We studied the mechanisms of tumor-Mphi interactions leading to Mphi activation. The results show that L5178Y mouse T cell lymphoma cells can prime naive mouse Mphi to subsequent LPS stimulation, resulting in increased NO production and antilymphoma effects in vitro. L5178Y cells, but not naive s...

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