نتایج جستجو برای: binding lectin deficiency

تعداد نتایج: 555860  

Journal: :Haematologica 2010
Michael Osthoff Alicia Rovó Martin Stern Doris Danner Alois Gratwohl André Tichelli Marten Trendelenburg

BACKGROUND Life-threatening infections are a major cause of death after allogeneic stem cell transplantation. Complement Mannose-binding lectin is a key component of innate immunity. Functional deficiency of mannose-binding lectin due to genetic polymorphism is frequent. Previous reports showed conflicting results with respect to the influence of functional mannose-binding lectin deficiency on ...

2016
Laura Choteau Francis Vasseur Frederic Lepretre Martin Figeac Corine Gower-Rousseau Laurent Dubuquoy Daniel Poulain Jean-Frederic Colombel Boualem Sendid Samir Jawhara

Mannose-binding lectin, together with mannose-associated serine proteases, activates the lectin pathway of the complement system and subsequent inflammatory mechanisms. An association between mannose-binding lectin deficiency and anti-Saccharomyces cerevisiae antibody levels is observed in Crohn's disease and this deficiency is frequently associated with a severe Crohn's disease phenotype. In t...

Journal: :The FASEB Journal 2021

The integrin α4β7 selectively regulates lymphocyte trafficking and adhesion in the gut gut-associated lymphoid tissues (GALT). Here we describe unexpected involvement of tyrosine phosphatase Shp1 B cell lectin CD22 (Siglec 2) regulation surface expression immunity. inhibited β7 endocytosis, enhancing display homing to GALT. In cells, associated a sialic acid-dependent manner with on target intr...

Journal: :Journal of immunology 2006
Ming Zhang Kazue Takahashi Elisabeth M Alicot Thomas Vorup-Jensen Benedikt Kessler Steffen Thiel Jens Christian Jensenius R Alan B Ezekowitz Francis D Moore Michael C Carroll

Reperfusion of ischemic tissues elicits an acute inflammatory response involving serum complement, which is activated by circulating natural IgM specific to self-Ags exposed by ischemia. Recent reports demonstrating a role for the lectin pathway raise a question regarding the initial events in complement activation. To dissect the individual roles of natural IgM and lectin in activation of comp...

2011
Bárbara Padilla-Docal Alberto J Dorta-Contreras Raisa Bu-Coifiu-Fanego René H Martínez-Alderete Olga Susana de Paula-Almeida Hansotto Reiber Jens Christian Jensenius

INTRODUCTION Eosinophilic meningitis, a potentially fatal disease caused by Angiostrongylus cantonensis, is considered an emerging infectious disease. CASE PRESENTATION Three Caucasian boys (aged five-years-old, 10-years-old and six-years-old) with a diagnosis of eosinophilic meningoencephalitis caused by Angiostrongylus cantonensis were studied. Serum immunoglobulin A (IgA), IgM, IgG, and co...

Journal: :Molecular immunology 2006
S Thiel P D Frederiksen J C Jensenius

Mannan-binding lectin (MBL) is a plasma protein of the innate immune system with the ability to initiate antimicrobial and inflammatory actions. MBL deficiency is common. More than 10% of the general population may, depending on definition, be classified as MBL deficient, underlining the redundancy of the immune system. Ongoing research attempt to illuminate at which conditions MBL deficiency m...

Journal: :Archives of disease in childhood 1998
J Aittoniemi M Baer E Soppi T Vesikari A Miettinen

OBJECTIVE To determine the prevalence of a mannan binding lectin (MBL) deficiency in children with increased susceptibility to infections and to investigate whether other coexisting immunodeficiencies affecting opsonisation are needed to render MBL deficiency clinically significant. PATIENTS AND METHODS 343 serum samples were collected from 266 children with repeated infections, a single epis...

Journal: :Archives of ophthalmology 2009
James C H Tan Mark J Lucarelli Daniel M Albert Lindell R Gentry

Comment. Deficiency of MBL has been correlated with a variety of infections in otherwise healthy individuals but may also enhance susceptibility to certain infections in persons receiving chemotherapy or those with secondary immunosuppression for other reasons. Genetic polymorphism explains the range of serum concentrations of MBL found in the general population, with severe serum MBL deficienc...

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