نتایج جستجو برای: MBL

تعداد نتایج: 1911  

Journal: :Journal of immunology 2009
Nannette Brouwer Florine N J Frakking Marianne D van de Wetering Michel van Houdt Margreet Hart Ilona Kleine Budde Paul F W Strengers Inga Laursen Gunnar Houen Dirk Roos Jens C Jensenius Huib N Caron Koert M Dolman Taco W Kuijpers

Mannose-binding lectin (MBL) deficiency is often associated with an increased risk of infection or worse prognosis in immunocompromised patients. MBL substitution in these patients might diminish these risks. We therefore performed an open, uncontrolled safety and pharmacokinetic MBL-substitution study in 12 pediatric oncology patients with chemotherapy-induced neutropenia. Twice weekly MBL inf...

Journal: :Molecular immunology 2006
Nannette Brouwer Koert M Dolman Rob van Zwieten Ed Nieuwenhuys Margreet Hart Lucien A Aarden Dirk Roos Taco W Kuijpers

The complement system is a humoral effector in the innate immune system. Three activation pathways exist in the complement system, known as the classical pathway, the lectin pathway and the alternative pathway. Dysfunction of lectin pathway activation is caused by MBL deficiency. MBL deficiency in a cohort of healthy Caucasian blood bank donors was investigated with MBL genotyping and MBL plasm...

Journal: :Immunobiology 2006
Meghan E McMullen Melanie L Hart Mary C Walsh Jon Buras Kazue Takahashi Gregory L Stahl

Recent evidence has implicated a role for the MBL-dependent lectin pathway in gastrointestinal and myocardial ischemia/reperfusion (I/R)-induced injury. However, previous studies have implicated IgM and the classical pathway as initiators of complement activation following I/R. Thus, we investigated the potential interaction between MBL and IgM leading to complement activation. Using surface pl...

Journal: :Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2008
Phoebe H Yager Zerong You Tao Qin Hyung-Hwan Kim Kazue Takahashi Alan B Ezekowitz Gregory L Stahl Michael C Carroll Michael J Whalen

Mannose binding lectin (MBL) initiates complement activation and exacerbates tissue damage after systemic ischemia/reperfusion. We tested the hypothesis that MBL activates complement and worsens outcome using two levels of controlled cortical impact (CCI) in mice. After moderate CCI (0.6 mm depth), MBL immunostaining was detected on injured endothelial cells of wild-type (WT) mice and C3d was d...

Journal: :Clinical advances in hematology & oncology : H&O 2013
Sameer A Parikh Neil E Kay Tait D Shanafelt

Monoclonal B-cell lymphocytosis (MBL) is a clonal B-cell disorder characterized by less than 5 × 109/L B lymphocytes in the peripheral blood, with a characteristic immunophenotype and no lymphadenopathy or organomegaly. The vast majority of MBL cases express the immunophenotype of chronic lymphocytic leukemia (CLL; CLL-like MBL), although non-CLL MBL also exists. CLL-like MBL, which is the focu...

Journal: :Molecular immunology 2006
Antonio Carlos Rosário Vallinoto Marcos Rogério Menezes-Costa Anna Elizabeth Martins Alves Luiz Fernando Almeida Machado Vânia Nakauth de Azevedo Lia Lobato Batista Souza Marluísa de Oliveira Guimarães Ishak Ricardo Ishak

Mannose-binding lectin (MBL) is a serum protein whose low concentration is associated with the occurrence of allele variants named MBL*B, MBL*C and MBL*D. The present study investigated the association between MBL gene polymorphism and the susceptibility to HIV-1 infection. The study of 145 HIV-1-infected subjects and 99 healthy controls showed the presence of alleles MBL*A, MBL*B and MBL*D, wh...

Journal: :Cytometry. Part B, Clinical cytometry 2010
Youn K Shim Dannie C Middleton Neil E Caporaso Jane M Rachel Ola Landgren Fatima Abbasi Elizabeth S Raveche Andy C Rawstron Alberto Orfao Gerald E Marti Robert F Vogt

BACKGROUND Individuals with monoclonal B-cell lymphocytosis (MBL) have been identified in clinic outpatients, in unaffected relatives of patients with chronic lymphocytic leukemia (CLL), and in general populations. MBL and its relationship with CLL have been actively investigated over the last decade. This report systematically reviews the prevalence of MBL in the context of the populations stu...

Journal: :The Journal of Experimental Medicine 2000
Ionita Ghiran Sergi F. Barbashov Lloyd B. Klickstein Sander W. Tas Jens C. Jensenius Anne Nicholson-Weller

Mannan-binding lectin (MBL), a member of the collectin family, is known to have opsonic function, although identification of its cellular receptor has been elusive. Complement C1q, which is homologous to MBL, binds to complement receptor 1 (CR1/CD35), and thus we investigated whether CR1 also functions as the MBL receptor. Radioiodinated MBL bound to recombinant soluble CR1 (sCR1) that had been...

Journal: :The Journal of biological chemistry 2004
Flemming Larsen Hans O Madsen Robert B Sim Claus Koch Peter Garred

Deficiency of human mannose-binding lectin (MBL) caused by mutations in the coding part of the MBL2 gene is associated with increased risk and severity of infections and autoimmunity. To study the biological consequences of MBL mutations, we expressed wild type MBL and mutated MBL in Chinese hamster ovary cells. The normal MBL cDNA (WT MBL-A) was cloned, and the three known natural and two arti...

2009
Mikael Bitsch Michael Christiansen Anne - Marie Engel Per Evald Holstein Tonny Karlsmark

© 2009 The Authors. doi: 10.2340/00015555-0582 Journal Compilation © 2009 Acta Dermato-Venereologica. ISSN 0001-5555 Sir, Mannan-binding lectin (MBL) is an important member of the innate immune system. Deficiency of MBL has been associated with increased propensity to infections, particularly in childhood (1). MBL deficiency is the most frequent immunodeficiency and 10–15% of the Caucasian norm...

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