Monoclonal Antibodies (mAb) in the Therapy of T-Cell Lymphomas

2012 ◽  
pp. 243-261
Author(s):  
Lapo Alinari ◽  
Pierluigi Porcu ◽  
Bertrand Coiffier
1987 ◽  
Vol 77 (2) ◽  
pp. 72-77 ◽  
Author(s):  
Bernhard F. Odermatt ◽  
Hans Knecht ◽  
Martin F. Hagen ◽  
Jürg Fehr ◽  
Jacques R. Rüttner

Author(s):  
Steven T. Rosen ◽  
A.Michael Zimmer ◽  
Robin Goldman-Leikin ◽  
Joanne M. Kazikiewicz ◽  
Mark S. Dykewicz ◽  
...  

1987 ◽  
Vol 18 (8) ◽  
pp. 808-814 ◽  
Author(s):  
John G. Strickler ◽  
Lawrence M. Weiss ◽  
Cedith M. Copenhaver ◽  
Jane Bindl ◽  
Robin McDaid ◽  
...  

Author(s):  
Mikihiro Shamoto

A detailed ultrastructural morphology of antigen-antibody reactions using monoclonal antibodies is very valuable, not only for accurate diagnosis, but also for the understanding of the character of malignant lymphomas. This is a report of ultrastructural immuno-histochemical analysis of T-cell lymphomas, with special reference to Japanese T-cell lymphomas (ATL).Biopsy specimens of lymph nodes from 30 patients with T-cell lymphomas, (including 20 patients with ATL) were used. Frozen sections of 10 u thickness were cut from specimens fixed in periodate-lysine-paraformaldehyde. The available antibodies were, OKT 3/Leu 4, OKT 4/Leu 3a, OKT 8, Tac, and FTF 148. The sections were placed on slides, and overlayed with appropriate diluted monoclonal antibodies and incubated for 2 hours. Then they were incubated with biotinylated horse anti-IgG for 2 hours, and in both an avidin-biotinylated peroxidase complex and a peroxidase mouse anti-peroxidase complex for 2 hours. They were fixed in 2% glutaraldehyde, then incubated with DAB hydrogen peroxide, and postfixed in 2% OsO4. The specimens were embedded in inverted gelatin capsules and cut with a diamond knife.


1980 ◽  
Vol 28 (8) ◽  
pp. 771-776 ◽  
Author(s):  
R Warnke ◽  
R Levy

Acetone-fixed frozen sections of reactive lymph node, spleen, three B cell lymphomas, and three T cell lymphomas were studied for the presence of Ia-like antigens and two T cell antigens. Detection of the binding of the hybridoma monoclonal antibodies to these antigens took advantage of the biotin-avidin interaction. The detection method employed a biotin conjugate of goat anti-mouse antibody and an avidin conjugate of horseradish peroxidase. B cell lymphoma cells stained for Ia. The cell lymphomas were shown to be heterogeneous for the expression of the two T cell antigens. these three antigens were generally not detectable after 10% formalin fixation of B-5 fixation. Detection of these antigens and the method employed should prove useful in the immunologic categorization of human lymphomas.


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