scholarly journals Successful Treatment of Experimental Western Equine Encephalomyelitis with Hyperimmune Rabbit Serum

1945 ◽  
Vol 35 (8) ◽  
pp. 815-823 ◽  
Author(s):  
Joseph Zichis ◽  
Howard J. Shaughnessy
Keyword(s):  
Successful Treatment ◽  
Rabbit Serum ◽  
Hyperimmune Rabbit

scholarly journals STUDIES ON HERPETIC INFECTION IN MICE

1946 ◽  
Vol 84 (5) ◽  
pp. 429-447 ◽  
Author(s):  
Charles A. Evans ◽  
Howard B. Slavin ◽  
George Packer Berry
Keyword(s):  
Nervous System ◽  
Immune Serum ◽  
Rabbit Serum ◽  
Herpetic Infection ◽  
Focus Of Infection ◽  
System 2 ◽  
The Central Nervous System ◽  
Foot Pad ◽  
Old Mice ◽  
Hyperimmune Rabbit

Two-week-old mice inoculated with herpes virus on the pad of a hind foot regularly developed paralysis of the infected limb followed by paraplegia and encephalitis terminating fatally 5 or 6 days after inoculation. Hyperimmune rabbit serum given intraperitoneally at the time virus was inoculated on the foot pad prevented the formation of an herpetic lesion of the foot pad. When the antiserum was given 12 hours after inoculation of the virus, a typical infection of the epithelium of the foot pad developed, but the virus was prevented from causing obvious signs of infection of the nervous system in many of the animals. Amputation of the foot 2 hours after the inoculation of the virus prevented the paralysis of the hind leg. Some of the mice died of a delayed encephalitis. Amputation of the foot at 24 hours neither prevented nor delayed the sequence of paralysis of the hind leg, encephalitis, and death. In order to study immune serum therapy of an infection of the nervous system uncomplicated by a peripheral focus of infection or by traumatic disturbance of the central nervous system, 2-week-old mice were inoculated on the foot pad, the infected feet were amputated 24 hours later, and the immune serum was administered at varying intervals thereafter. Using litter mate controls and statistically significant numbers of mice, it was shown that hyperimmune rabbit serum, administered during the first one-third of the incubation period, retards and, in some cases, arrests the progress of herpetic infection within the nervous system.

scholarly journals Light microscopic, immunohistochemical localization of the pia-glial basal lamina.

1980 ◽  
Vol 28 (4) ◽  
pp. 347-353 ◽  
Author(s):  
T F Kowalski ◽  
H L Vahlsing ◽  
E R Feringa
Keyword(s):  
Basal Lamina ◽  
Wistar Rats ◽  
Staining Technique ◽  
Immunohistochemical Localization ◽  
Basement Membrane Zone ◽  
Rabbit Serum ◽  
Antibody Technique ◽  
Antigenic Source ◽  
Hyperimmune Rabbit ◽  
Different Tissues

The current histologic methods for studying the pia-glial basal lamina (BL) are inappropriate for high contrast, permanent light microscopy preparation. We have developed a staining technique for epithelial BL which is highly specific, extremely sensitive, permanent, relatively inexpensive, and suitable for light or electron microscopy (EM). Central nervous system (CNS) basement membrane zone (BMZ) antigens were isolated by the technique of Meezan (1975) from female albino Wistar rats. Using this CNS BMZ preparation as an antigenic source, a hyperimmune rabbit serum was developed. This serum was exhaustively adsorbed with rat splenic pulp to remove undesirable antibodies to endothelial BL and collagen. The peroxidase-antiperoxidase indirect antibody technique was used to test the staining specificity of this splenic adsorbed serum on different tissues containing BLs of known origin and/or function. The results indicated that this BL staining technique was specific for epithelial BL of the rat and of some other species.

scholarly journals Phage Lytic Enzyme Cpl-1 as a Novel Antimicrobial for Pneumococcal Bacteremia

2003 ◽  
Vol 71 (11) ◽  
pp. 6199-6204 ◽  
Author(s):  
Jutta M. Loeffler ◽  
Svetolik Djurkovic ◽  
Vincent A. Fischetti
Keyword(s):  
Streptococcus Pneumoniae ◽  
Treatment Efficacy ◽  
Lytic Enzyme ◽  
Rabbit Serum ◽  
Resistant Bacteria ◽  
Intravenous Therapy ◽  
Antibiotic Resistant ◽  
Pneumococcal Bacteremia ◽  
Hyperimmune Rabbit

ABSTRACT Streptococcus pneumoniae is becoming increasingly antibiotic resistant worldwide, and thus new antimicrobials are badly needed. We report the use of Cpl-1, the lytic enzyme of a pneumococcal bacteriophage, as an intravenous therapy for pneumococcal bacteremia in a mouse model. A 2,000-μg dose of Cpl-1 reduced pneumococcal titers from a median of log10 4.70 CFU/ml to undetectable levels (<log10 2.00 CFU/ml) within 15 min. This dose given 1 h after intravenous infection led to 100% survival at 48 h, compared to the 20% survival of buffer-treated controls. In advanced bacteremia, treatment with two doses at 5 and 10 h still resulted in significantly longer survival (P < 0.0001) and a hazard ratio of 0.29 (95% confidence interval, 0.04 to 0.35). The enzyme is immunogenic, but the treatment efficacy was not significantly diminished after previous intravenous exposure of mice and hyperimmune rabbit serum did not neutralize the activity. Cpl-1 is also very effective as a topical nasal treatment against colonization by S. pneumoniae. In vitro, the enzyme is active against many serotypes of S. pneumoniae, independent of their penicillin resistance, and it is very specific for this species. Bacteriophage enzymes are unusual but extremely effective antimicrobials and represent a new weapon against infections with resistant bacteria.

Coproantigen detection for immunodiagnosis of echinococcosis and taeniasis in dogs and humans

Parasitology ◽  
1992 ◽  
Vol 104 (2) ◽  
pp. 347-355 ◽  
Author(s):  
J. C. Allan ◽  
P. S. Craig ◽  
J. Garcia Noval ◽  
F. Mencos ◽  
D. Liu ◽  
...  
Keyword(s):  
Experimental Infection ◽  
False Positive ◽  
Time Course ◽  
Field Studies ◽  
Field Application ◽  
Rabbit Serum ◽  
Somatic Antigen ◽  
Faecal Samples ◽  
Specific Antigens ◽  
Hyperimmune Rabbit

SUMMARYThree ELISA assays, based on hyperimmune rabbit serum raised against adult cestode somatic antigen, were applied in this study for the detection ofTaenia- andEchinococcus-specific antigens in host faeces. The first assay, using an antiserum againstTaenia pisiformisantigen extract, was used in a time-course ofT. pisiformisexperimental infection in dogs. The assay was shown to be considerably more sensitive than microscopical detection of eggs in faeces. Antigen was present in faeces before patency and antigen levels were independent ofT. pisiformisegg output. The second assay, involving a test for human taeniasis based on antibodies againstT. solium, was applied in two field studies carried out in China and Guatemala. The test was highly specific, no false positive reactions occurred with human faecal samples and the test was capable of diagnosing individuals who would not have been detected by coproscopy or treatment to recover the tapeworm. A third assay was designed forE. granulosusand demonstrated 87·5% sensitivity and 96·5% specificity with samples from naturally and experimentally infected dogs withEchinococcusorTaeniainfections. In both the humanTaeniaand canineEchinococcusstudies antigen could be detected in faecal samples from infected hosts stored in 5% formalin for 6 months. Further refinements to these tests for field application are discussed.

Artifact-free electron microscopic immunocytochemistry on rat brain tissue

1991 ◽  
Vol 49 ◽  
pp. 272-273
Author(s):  
Veronika Burmeister ◽  
N. Ludvig ◽  
P.C. Jobe
Keyword(s):  
Microscopic Examination ◽  
Free Electron ◽  
Electron Microscopic Examination ◽  
Ultrastructural Localization ◽  
Rabbit Serum ◽  
Electron Microscopic ◽  
Electron Microscopic Immunocytochemistry ◽  
Phosphate Buffered Saline ◽  
Rat Brain Tissue ◽  
Immune Rabbit

Electron microscopic immunocytochemistry provides an important tool to determine the ultrastructural distribution of various molecules in both normal and pathologic tissues. However, the specific immunostaining may be obscured by artifactual immunoreaction product, misleading the investigator. Previous observations show that shortening the incubation period with the primary antibody from the generally used 12-24 hours to 1 hour substantially reduces the artifactual immunostaining. We now extend this finding by the demonstration of artifact-free ultrastructural localization of the Ca2/calmodulindependent cyclic nucleotide phosphodiesterase (CaM-dependent PDE) immunoreactivity in brain.Anesthetized rats were perfused transcardially with phosphate-buffered saline followed by a fixative containing paraformaldehyde (4%) and glutaraldehyde (0.25%) in PBS. The brains were removed, and 40μm sections were cut with a vibratome. The sections were processed for immunocytochemistry as described by Ludvig et al. Both non-immune rabbit serum and specific CaM-dependent PDE antibodies were used. In both experiments incubations were at one hour and overnight. The immunostained sections were processed for electron microscopic examination.

Detection of Viral Antigens in Mouse and Rat Tumor Cells by Immunoelectron Microscopy Following Periodate-Lysine-Paraformaldehyde (PLP) Fixation

1976 ◽  
Vol 34 ◽  
pp. 252-253
Author(s):  
Y. Ohtsuki ◽  
G. Seman ◽  
J. M. Bowen ◽  
M. Scanlon ◽  
L. Dmochowski
Keyword(s):  
Immunoelectron Microscopy ◽  
Mammary Tumor ◽  
Type A ◽  
Rabbit Serum ◽  
Virus Particles ◽  
Viral Antigens ◽  
Culture Cells ◽  
Mouse Mammary Tumor ◽  
Tumor Virus ◽  
Immunoperoxidase Labeling

Recently, periodate-lysine-paraformaldehyde (PLP) fixation was reported for immunoelectron microscopy (1). In PLP fixation, carbohydrates are oxidized by periodate and cross-linked by lysine; paraformaldehyde stabilizes proteins and lipids. By using PLP fixation, intracytoplasmic type A viral antigens have been previously demonstrated by immunoperoxidase labeling (2). In the present study, PLP fixation has been applied for the detection of the same antigens in mouse mammary tumor culture cells by both immunoferritin and immunoperoxidase methods. Rabbit anti-intracytoplasmic type A virus serum (anti-A), kindly provided by Dr. M. Muller (3), rabbit anti-strain A mouse mammary tumor virus (anti-MMTV) and preimmune rabbit serum as control were used to detect viral antigens in cells of C3H/HeJ strain mouse mammary tumor culture. Attempts have been also made to demonstrate peroxidase labeling of type C virus particles in frozen sections of an SD-MSV-induced NZB rat bone tumor tissue by rabbit anti-MuLV serum.

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