Identification of tumour cells in CSF using monoclonal antibodies

Pathology ◽  
1984 ◽  
Vol 16 (4) ◽  
pp. 480
Author(s):  
W.W. Hancock ◽  
R.C. Atkins ◽  
G. Medley ◽  
M. Drake
1988 ◽  
Vol 16 (3) ◽  
pp. 373-374
Author(s):  
ELIZABETH MORAN ◽  
RICHARD O'KENNEDY ◽  
JACK PHILLIPS ◽  
GEORGE KARR

1992 ◽  
Vol 3 (suppl b) ◽  
pp. 20-25
Author(s):  
Robert O Dillman

Monoclonal antibodies may modulate immune and/or biological responses alone, or as carriers of specific agents. Monoclonal antibodies directed against tumours may be indirectly cytotoxic by modulation of antibody-dependent, cell-mediated cytotoxicity or complement-mediated cytotoxicity. Monoclonal antibodies directed against certain tumour cell receptors may alter the biological behaviour of tumour cells such as blocking or downregulation of growth factors essential to tumour cell proliferation. Monoclonal antibodies directed to certain receptors on host immune cells. such as the CD3 receptor on T lymphocytes. may activate those cells and increase their cytotoxicity. Antitumour monoclonal antibodies can serve as carriers of interferons, interleukin-2, tumour necrosis factor and other lymphokines and cytokines to modulate selectively the cytotoxic potential of immune cells in the vicinity of tumour cells. Cytotoxic chemotherapy agents conjugated to antitumour monoclonal antibodies may be processed differently so that they bypass certain mechanisms of drug resistance. The penultimate application of monoclonal antibodies in cancer therapy is to combine various monoclonal antibodies and immunoconjugates for selective combination therapy based on known antigenic tumour cell determinants and the status of the host immune system.


1989 ◽  
Vol 60 (6) ◽  
pp. 855-860 ◽  
Author(s):  
LG Durrant ◽  
RA Robins ◽  
KC Ballantyne ◽  
RA Marksman ◽  
JD Hardcastle ◽  
...  

2007 ◽  
Vol 9 (34) ◽  
pp. 1-21 ◽  
Author(s):  
Erik Johnson ◽  
Shannon M. Dean ◽  
Paul M. Sondel

AbstractAlthough great advances have been made in the treatment of low- and intermediate-risk neuroblastoma in recent years, the prognosis for advanced disease remains poor. Therapies based on monoclonal antibodies that specifically target tumour cells have shown promise for treatment of high-risk neuroblastoma. This article reviews the use of monoclonal antibodies either as monotherapy or as part of a multifaceted treatment approach for advanced neuroblastoma, and explains how toxins, cytokines, radioactive isotopes or chemotherapeutic drugs can be conjugated to antibodies to enhance their effects. Tumour resistance, the development of blocking antibodies, and other problems hindering the effectiveness of monoclonal antibodies are also discussed. Future therapies under investigation in the area of immunotherapy for neuroblastoma are considered.


1992 ◽  
Vol 34 (6) ◽  
pp. 407-413 ◽  
Author(s):  
Marie-José Palisson ◽  
Anne Altemeyer ◽  
Isabelle Moosbrugger ◽  
Stéphanie Warter ◽  
Georges Hauptmann ◽  
...  

Nature ◽  
1981 ◽  
Vol 290 (5802) ◽  
pp. 145-146 ◽  
Author(s):  
Hildur E. Blythman ◽  
Pierre Casellas ◽  
Olivier Gros ◽  
Pierre Gros ◽  
Franz K. Jansen ◽  
...  

1985 ◽  
Vol 61 (1) ◽  
pp. 21-30 ◽  
Author(s):  
A. K. Ghosh ◽  
W. N. Erber ◽  
C. S. R. Hatton ◽  
N. T. J. O'Connor ◽  
B. Falini ◽  
...  

The Lancet ◽  
1983 ◽  
Vol 322 (8352) ◽  
pp. 739-740 ◽  
Author(s):  
W HANCOCK

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