DETERMINATION OF ANTIBODY TITERS AGAINST SOLUBLE ANTIGEN BY INDIRECT FLUORESCENT ANTIBODY (IFA) ASSAY USING LATEX PARTICLES COUPLED WITH SOLUBLE ANTIGEN: A PRELIMINARY STUDY

2013 ◽  
Vol 34 (1) ◽  
pp. 39-48 ◽  
Author(s):  
Takashi Kuribayashi ◽  
Tetsurou Seita ◽  
Toshio Honjyo ◽  
Katsuhito Kawato ◽  
Kayoko Takada ◽  
...  
PEDIATRICS ◽  
1972 ◽  
Vol 49 (4) ◽  
pp. 612-614
Author(s):  
Stephen H. Zinner ◽  
William M. McCormack ◽  
Yhu-Hsiung Lee ◽  
Marguerite H. Zuckerstatter ◽  
A. Kathleen Daly

Puerperal bacteremia and neonatal sepsis due to Haemophilus parainfluenzae is described in a mother and her infant. Indirect fluorescent antibody studies for specific IgM antibody directed against the H. parainfluenzae were performed on maternal and infant sera. The rise in infant IgM antibody titers suggested that the infant acquired the infecting organism during labor or delivery. H. parainfluenzae has not previously been implicated as a pathogen in either puerperal or neonatal sepsis.


1992 ◽  
Vol 4 (2) ◽  
pp. 144-147 ◽  
Author(s):  
In J. Yoon ◽  
Han S. Joo ◽  
William T. Christianson ◽  
Hyun S. Kim ◽  
James E. Collins ◽  
...  

An indirect fluorescent antibody (IFA) test was developed and standardized to detect and quantitate antibody for swine infertility and respiratory syndrome (SIRS) virus in swine sera. Test results were evaluated using sera of pigs infected both experimentally and naturally with SIRS virus. The IFA test used swine alveolar macrophage (SAM) monolayers prepared in 96-well microplates and infected with SIRS virus. The monolayers were incubated with test sera, washed, and stained with fluorescein isothiocyanate-labeled rabbit anti-swine IgG. After another wash step, the monolayers were examined under a fluorescent microscope. A noninfected SAM control well was included for each sample. The antibody titers for each serum sample were recorded as the highest serum dilutions with specific cytoplasmic fluorescence but no fluorescence in the control wells. To evaluate the test, sera of 4 6-week-old pigs that had been infected with SIRS virus, 2 contact pigs, and 13 experimentally infected sows were used. In the experimentally infected pigs, antibody was first detected at 7 days postexposure (PE) and peaked (1:256–1,024) between 11 and 21 days PE. All 13 sow sera were negative at time of infection but were positive (1:64-> 1: 1,024) at 14–26 days PE. Seven hundred twenty sera collected from 25 different swine farms with or without a history of SIRS were also tested. Of 344 sera from 15 swine farms with a clinical history of SIRS, 257 (74.7%) sera had IFA titers ≥ 1:4, whereas 371 (98.7%) of 376 sera from herds with no history of SIRS were negative. The present results indicate that the IFA is a useful test for the detection and quantitation of SIRS virus antibody in swine sera.


1981 ◽  
Vol 18 (5) ◽  
pp. 672-683 ◽  
Author(s):  
W. C. Hall ◽  
J. D. White ◽  
R. A. Kishimoto ◽  
R. E. Whitmire

Athymic nude mice and euthymic littermate controls were exposed to 104 Coxiella burnetii organisms by small-particle aerosol. Antibody response with and without 2-mercaptoethanol treatment of serum was determined at various intervals after infection and serial kills were done to determine morphologic changes in both mouse phenotypes. Total antibody titers determined by the indirect fluorescent antibody technique to phase I and phase II C. burnetii were identical for both groups of mice. Microagglutinin titers determined on days 28 and 33 were abolished by 2-mercaptoethanol treatment of serum from both phenotypes, indicating that the antibody probably resided in the IgM fraction. Microscopically, the reaction to C. burnetii infection was similar in nude and euthymic mice on days 7 and 14. Later, the number and size of lesions attributable to Q fever diminished in euthymic mice. Infection was progressive in nude mice, with macrophage infiltration of most tissues, especially spleen and liver. Numerous rickettsiae were seen by immunofluorescence and electron microscopy in phagocytic vesicles of macrophages, many of which were dilated, giving the macrophage a vacuolated appearance. Results suggest that clearance of C. burnetii infection in mice is dependent upon thymus-derived lymphocytes.


1976 ◽  
Vol 3 (6) ◽  
pp. 637-639
Author(s):  
A J Parkinson ◽  
J Kalmakoff

Commercially prepared fluorescein-labeled antihuman antibodies were labed with 125I and used to compre specific herpes simplex virus antibody titers as determined by indirect fluorescent antibody and radioimmunoassay techniques. Total virus-specific immunoglobulin and virus-specific immunoglobulin G titers did not vary by more than one twofold dilution when compared by the two methods.


1977 ◽  
Vol 5 (3) ◽  
pp. 320-325
Author(s):  
T K Lee ◽  
H D Hutchinson ◽  
D W Ziegler

Rabies humoral antibodies were induced in eight New Zealand rabbits by a single intramuscular injection of inactivated suckling mouse brain rabies vaccine. The primary response to immunization was measured in blood samples taken at selected intervals for 6 months. The anamnestic response was measured in blood samples obtained 2 weeks after the rabbits received a booster immunization. The humoral antibody concentrations were measured by the rapid-fluorescent-focus-inhibition technique (RFFIT), indirect fluorescent-antibody assay (IFA), and indirect radioimmunoassay (RIA). The maximal neutralizing antibody titers as measured by RFFIT were attained by the 4th week and persisted into the 24th week. After booster immunization the antibody response was almost 10-fold higher than the highest level attained in the primary response. The antibody levels as measured by IFA and RIA were similar, but the titers as measured by either procedure were almost 10-fold lower than those determined by RFFIT. After booster immunizations the antibody levels, as measured by IFA and RIA, were three- and sixfold higher, respectively, than the maximal levels attained in the primary response. Twenty-two human serum specimens were tested by the same serological procedures, with disparate results. Both RIA and RFFIT effectively differentiated antirabies-positive sera from antirabies-negative sera.


1978 ◽  
Vol 7 (4) ◽  
pp. 385-388
Author(s):  
M B Graham ◽  
W A Falkler

White male New Zealand rabbits were immunized with soluble antigen preparations (SP) of the following gram-positive anaerobic cocci: Peptostreptococcus anaerobius ATCC 27337 and VPI 5737; P. micros VPI 2618; Streptococcus morbillorum ATCC 27527; P. parvulus VPI 5229; and P. productus ATCC 27340. SP were reacted with homologous and heterologous rabbit antisera in immunodiffusion, immunoelectrophoresis, indirect fluorescent-antibody, and tanned-cell passive hemagglutination tests. Even though each antiserum reacted strongly with its homologous SP, no interspecies reactivity was observed except between P. productus antisera and P. parvulus SP by the passive hemagglutination test. Antisera prepared to both strains of P. anaerobius reacted with the other strain in all serological tests.


Science ◽  
1964 ◽  
Vol 145 (3635) ◽  
pp. 943-945 ◽  
Author(s):  
G. C. Brown ◽  
H. F. Maassab ◽  
J. A. Veronelli ◽  
T. J. Francis

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