Immunohistochemical Staining of Rabies Virus Antigen with Monoclonal and Polyclonal Antibodies in Paraffin Tissue Sections

1988 ◽  
Vol 35 (1-10) ◽  
pp. 247-255 ◽  
Author(s):  
W. Feiden ◽  
E. Kaiser ◽  
L. Gerhard ◽  
E. Dahme ◽  
B. Gylstorff ◽  
...  
Author(s):  
A. G. Mukhamedzhanova ◽  
◽  
M. A. Efimova ◽  
A. N. Chernov ◽  
K. S. Khaertynov ◽  
...  

1995 ◽  
Vol 32 (3) ◽  
pp. 309-311 ◽  
Author(s):  
G. L. Foley ◽  
J. F. Zachary

A 1-year-old mixed breed heifer was presented to the Veterinary Medical Teaching Hospital at the University of Illinois with a 3-day history of abnormal mentation and aggressive behavior. Based on the history and clinical examination, euthanasia and necropsy were recommended. The differential diagnoses included rabies, pseudorabies, and a brain abscess. The brain was removed within 60 minutes of death, and the section submitted for fluorescent antibody testing was positive for rabies virus antigen. Residual brain tissue was immersion fixed in 10% neutral buffered formalin. Histologic examination revealed a marked perivascular and meningeal lymphocytic meningoencephalitis and locally extensive spongiform change of the gray matter affecting the neuropil and neuron cell bodies. The most severely affected regions with spongiform change were the thalamus and cerebral cortex. No Negri bodies were found in any sections. Since the outbreak of bovine spongiform encephalopathy (BSE) in the United Kingdom, there has been an increased surveillance of bovine neurologic cases in an effort to assess if BSE has occurred in the USA. In areas where rabies virus is endemic, rabies should be included as a possible differential diagnosis in cases of spongiform changes of the central nervous system.


1989 ◽  
Vol 37 (5) ◽  
pp. 611-615 ◽  
Author(s):  
S Ito ◽  
A Iwasaki ◽  
J Syundo ◽  
Y Tamura ◽  
S Kishi ◽  
...  

Human liver guanase was purified and a specific antibody against it was raised in rabbits. The antiserum formed a single precipitin line with human liver extract, and also completely inhibited the activity of the liver enzyme. An immunoblotting study showed that the antibody bound specifically to one band of protein with guanase activity and not to other proteins. Therefore, we concluded that this antiserum against the liver enzyme was suitable for use in immunohistochemical demonstration of guanase. In tissue sections, the immunohistochemical reaction with this antibody was positive in the same locations as the histochemical guanase reaction with DAB (3,3'-diaminobenzidine tetrahydrochloride).


1993 ◽  
Vol 79 (2) ◽  
pp. 128-132 ◽  
Author(s):  
Marcello Guarino ◽  
Salvatore Squillaci ◽  
Domenico Reale ◽  
Giorgio Micoli

Aims Eight sarcomatoid carcinomas from various anatomical locations were investigated by immunohistochemical staining to laminin, type IV collagen and heparan sulfate proteoglycan, to study the characteristics of basement membranes at the interface between carcinomatous and sarcomatous tissues. Methods Paraffin wax embedded tissue sections from representative tumor samples have been stained with specific antibodies, using the peroxidase-antiperoxidase technique. Results In all cases several interruptions or discontinuities of the basement membrane staining pattern were seen. In 4 cases, larger defects or complete loss of staining was also noted. At these places, the boundaries between carcinomatous and sarcomatous tissue were often blurred. Conclusions Disruption and loss of basement membranes at interface between carcinomatous and sarcomatous tissues is a frequent finding in sarcomatoid carcinomas. These changes could be consistent with an epithelial origin of the sarcomatous component in these tumors by means of an epithelial-mesenchymal conversion mechanism.


1992 ◽  
Vol 36 (2) ◽  
pp. 341 ◽  
Author(s):  
S. D. Fitzgerald ◽  
W. M. Reed ◽  
T. Burnstein

2011 ◽  
Vol 31 (2) ◽  
Author(s):  
A Garba ◽  
SI Oboegbulem ◽  
AU Junaidu ◽  
AA Magaji ◽  
JU Umoh ◽  
...  

1999 ◽  
Vol 111 (2) ◽  
pp. 143-151 ◽  
Author(s):  
David Trick ◽  
Jens Decker ◽  
Hermann-Josef Groene ◽  
Matthias Schulze ◽  
H. Wiegandt

1995 ◽  
Vol 7 (4) ◽  
pp. 444-450 ◽  
Author(s):  
Scott D. Fitzgerald ◽  
Willie M. Reed ◽  
Richard M. Fulton

An immunohistochemical staining technique was developed to detect polyomaviral antigens of budgerigar fledgling disease in formalin-fixed tissue sections. This technique used an indirect avidin-biotin, alkaline phosphatase labeling system with a mixture of monoclonal antibodies developed against the virus major capsid protein. The staining technique was applied retrospectively to 24 avian accessions which were originally diagnosed as budgerigar fledgling disease or avian polyomavirus infection based on microscopic findings including typical intranuclear inclusions. Immunohistochemical staining resulted in positive reactions in some tissues from 17 of 24 cases. The tissues most frequently containing typical intranuclear inclusions or positive immunohistochemical staining were the spleen, liver, and kidney. Neither of the 2 nonpsittacine cases was positive immunohistochemically. This technique may be used either as a rapid test on routinely processed diagnostic samples to confirm the presence of avian polyomavirus or for pathogenesis research studies.


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