Introduction to mannan-binding lectin

2003 ◽  
Vol 31 (4) ◽  
pp. 745-747 ◽  
Author(s):  
D.C. Kilpatrick

Mannan-binding lectin (MBL) was first discovered as a plasma opsonin for baker's yeast and was independently characterized biochemically. It belongs to the small subfamily of collectins: C-type lectins possessing a collagen-like domain. MBL is synthesized by the liver and secreted into the bloodstream. It is believed to be an important component of innate immunity, acting as an ante-antibody and/or as a disease modifier. It is thought to influence disorders as diverse as meningococcal disease, rheumatoid arthritis, cystic fibrosis and recurrent miscarriage. Lack of MBL may be most relevant in the context of a co-existing secondary immune deficiency. Replacement therapy, first carried out 30 years ago with unfractionated plasma, appears promising. The development of a recombinant product should permit the extension of MBL therapy to randomized clinical trials of sufficient size to provide clear evidence about the physiological significance of this intriguing glycoprotein.

2003 ◽  
Vol 25 (4) ◽  
pp. 33-34 ◽  
Author(s):  
David Kilpatrick

Mannan-binding lectin (MBL) is perhaps the best known of the collectins, a subfamily of C-type lectins possessing an additional collagen-like domain. MBL is thought to be an important component of innate immunity. Since the discovery, around 15 years ago, that MBL was identical to a factor responsible for the opsonization of baker's yeast in vitro, a large number of disease-association studies have been conducted. Most of these investigations support the view that MBL can influence susceptibility to, or affect the course of, many diseases. These include bacterial infections, rheumatoid arthritis, cystic fibrosis and recurrent miscarriage. This meeting was arranged to bring together scientists and clinicians to review the clinical significance of MBL, and to consider the most appropriate target disorders for MBL-replacement therapy.


2003 ◽  
Vol 31 (4) ◽  
pp. 763-767 ◽  
Author(s):  
J.C. Jensenius ◽  
P.H. Jensen ◽  
K. McGuire ◽  
J.L. Larsen ◽  
S. Thiel

Mannan-binding lectin (MBL) is a plasma protein involved in the innate immune response. It binds to a number of micro-organisms and promotes killing of these through complement activation either directly or through opsonization. Clinical evidence indicates that in a variety of situations genetically determined low MBL levels are associated with increased susceptibility to infections. Infusions of plasma-derived MBL into MBL-deficient individuals was found to be safe in preliminary trials, but we considered that sufficient production and product safety could only be achieved through synthesis of recombinant MBL. A transfected human cell line produces MBL showing the same biological activity as plasma-derived MBL, and an essentially identical profile on MS. The production has been scaled up and clinical trials will start this year.


2011 ◽  
Vol 13 (2) ◽  
pp. R65 ◽  
Author(s):  
Saedis Saevarsdottir ◽  
Bo Ding ◽  
Kristjan Steinsson ◽  
Gerdur Grondal ◽  
Helgi Valdimarsson ◽  
...  

2006 ◽  
Vol 12 (Supplement) ◽  
pp. S43-S44
Author(s):  
Carlos Abud-Mendoza ◽  
L W Moreland ◽  
K Bahrt ◽  
J-C Becker ◽  
R Aranda ◽  
...  

2019 ◽  
Vol 2 (11) ◽  
pp. e1914745 ◽  
Author(s):  
Adrienne Strait ◽  
Francine Castillo ◽  
Sonam Choden ◽  
Jing Li ◽  
Evans Whitaker ◽  
...  

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