S caleup and Virus Clearance Studies on Virus Filtration in Monoclonal Antibody Manufacture

2001 ◽  
pp. 347-370
2014 ◽  
Vol 112 (3) ◽  
pp. 633-637 ◽  
Author(s):  
Andreas Wieser ◽  
Andreas Berting ◽  
Christian Medek ◽  
Gerhard Poelsler ◽  
Thomas R. Kreil

2020 ◽  
Author(s):  
David M. Bohonak ◽  
Ushma Mehta ◽  
Eric R. Weiss ◽  
Greg Voyta

PLoS ONE ◽  
2017 ◽  
Vol 12 (1) ◽  
pp. e0169139 ◽  
Author(s):  
Hyo-Jeong Lee ◽  
Jeong-Yoon Lee ◽  
Min-Hee Park ◽  
Joo-Young Kim ◽  
Jun Chang

2009 ◽  
Vol 90 (5) ◽  
pp. 1119-1123 ◽  
Author(s):  
Congrong Miao ◽  
Gertrud U. Radu ◽  
Hayat Caidi ◽  
Ralph A. Tripp ◽  
Larry J. Anderson ◽  
...  

Therapeutic treatment with a non-neutralizing monoclonal antibody (mAb) (131-2G) specific to respiratory syncytial virus (RSV) G glycoprotein mediates virus clearance and decreases leukocyte trafficking and interferon gamma (IFN-γ) production in the lungs of RSV-infected mice. Its F(ab′)2 component only mediates decreased leukocyte trafficking and IFN-γ production without reducing virus replication. Thus, this mAb has two independent actions that could facilitate treatment and/or prevention of RSV infection by reducing both virus replication and virus-induced pulmonary inflammation.


2009 ◽  
Vol 25 (2) ◽  
pp. 483-491 ◽  
Author(s):  
Bruno F. Marques ◽  
David J. Roush ◽  
Kent E. Göklen

1996 ◽  
Vol 14 (5) ◽  
pp. 651-652 ◽  
Author(s):  
Holger Maerz ◽  
Sven Oliver Hahn ◽  
Anke Maassen ◽  
Helga Meisel ◽  
Dirk Roggenbuck ◽  
...  

Author(s):  
Douglas R. Keene ◽  
Robert W. Glanville ◽  
Eva Engvall

A mouse monoclonal antibody (5C6) prepared against human type VI collagen (1) has been used in this study to immunolocalize type VI collagen in human skin. The enbloc method used involves exposing whole tissue pieces to primary antibody and 5 nm gold conjugated secondary antibody before fixation, and has been described in detail elsewhere (2).Biopsies were taken from individuals ranging in age from neonate to 65 years old. By immuno-electron microscopy, type VI collagen is found to be distributed as a fine branching network closely associated with (but not attached to) banded collagen fibrils containing types I and III collagen (Fig. 1). It appears to enwrap fibers, to weave between individual fibrils within a fiber, and to span the distance separating fibers, creating a “web-like network” which entraps fibers within deep papillary and reticular dermal layers (Fig. 2). Relative to that in the dermal matrix, the concentration of type VI collagen is higher around endothelial basement membranes limiting the outer boundaries of nerves, capillaries, and fat cells (Fig. 3).


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