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Results for “HEMAGGLUTINATION INHIBITION TESTS”

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At least 19 recordsLinked to original sources
PubMedDate not supplied

[Study of the correlation between neutralization tests and hemagglutination inhibition tests in determinations of mumps virus antibodies].

In order to find out possibilities of wide application of the hemagglutination-inhibition (HI) test for determination of antibody to mumps virus, correlations between neutralization test (NT) and HI test was studied. Antibody to mumps virus was detected by parallel titrations of sera and gamma globulins in HI and NT tests in two experimental series each of which used various modifications of these tests. Statistically significant strong correlation was established between these tests.

Antibodies, Viral↗
PubMed1977

A simplified determination of the urinary luteinizing hormone surge using the hemagglutination inhibition test.

The hemagglutination-inhibition test for urinary luteinizing hormone (LH) has been modified so that the test for LH surge can be assayed in 1 day. A first morning voided urine specimen submitted to the laboratory can be analyzed in 5 hours by ordinary bench procedures. This modification involves a 20-fold reduction, as compared with the older procedure, of the duration of incubation of the urine-antiserum mixture. Another modification is the choice of aliquots which are adaptable to automatic pipetting. Only a single dilution of urine is necessary to determine LH surge for the anticipation of ovulation. Daily LH determinations on 12 normally menstruating women (av. cycle 28.18 days) reveal consistent patterns. For the 40 cycles studied LH surge occurred 14.29 days (av.) prior to the onset of the next menstruation and coincided with the rise in basal body temperature. One woman with an unusually high incidence of familial twinning showed two large LH surges in each consecutive cycle.

Adult↗
PubMedDate not supplied

Rapid serotyping of infectious bronchitis virus isolates with the hemagglutination-inhibition test.

The hemagglutination-inhibition (HI) test was evaluated as a method of typing recent suspect infectious bronchitis virus (IBV) isolates. Hemagglutination (HA) antigen was prepared from each isolate by phospholipase C treatment of virus concentrated from allanto-amniotic fluids of infected chicken embryos. An HI test was run with the HA antigen of each isolate against a battery of 17 antisera that had been prepared against different IBV strains classified by virus neutralization (VN). The HI test identified Ark 99 and Holland isolates that were similar to strains previously classified by VN. Two isolates included in this study were not inhibited by any of the reference antisera and therefore appeared to be antigenically different. The isolates were also evaluated by VN, and the results of the VN and HI methods agreed. Therefore the results suggest that the HI test can be useful for making a rapid, presumptive identification of new IBV isolates.

Animals↗
PubMed1996

[Comparison between the plaque reduction neutralization test and the hemagglutination inhibition test in determination of human anti-measles antibodies].

In order to evaluate the difference between plaque reduction neutralization test (PNt) and hemagglutination inhibition (HI) test on human anti-measles antibodies, pre- and postimmunization sera collected from 328 infants aged 3-6 months who were immunized with Shanghai 191 measles vaccine, were detected by both methods. The results demonstrated that PNt was more sensitive than HI when they were used to measure the pre-immunization sera. No significant difference was found between these two methods when they were used to measure the post-immunization sera. PNt can be used to test low level maternal anti-measles antibodies in infants, especially for estimating the effect of maternal anti-measles antibodies on the immunogenicity of measles vaccine.

Antibodies, Viral↗
PubMed1993

Distinction between Aujeszky's disease virus-infected and vaccinated pigs by hemagglutination-inhibition test.

A hemagglutination-inhibition (HI) test was applied to distinguish virulent Aujeszky's disease virus infected pigs from those immunized with a glycoprotein gIII deletion vaccine. The vaccine strain, dlg92/dltk, did not have hemagglutination activity with mouse erythrocytes and the pigs vaccinated five times with the dlg92/dltk strain failed to develop HI antibody, although they developed neutralizing antibody with 128 to 512 titers to Aujeszky's disease virus. On the other hand, these pigs produced HI antibody 1 to 2 weeks after virulent virus inoculation. Thus the animals infected with virulent strain were easily differentiated from the animals immunized with the gIII deletion vaccine.

Animals↗
PubMed1968

An improved diluent for rubella hemagglutination and hemagglutination-inhibition tests.

Rubella hemagglutinating (HA) antigen was prepared in BHK-21 tissue as 5% cell suspensions and from unconcentrated and 20x concentrated infected supernatant fluids. In some instances, unconcentrated fluids were treated with Tween 80 and ether; cell suspensions were treated with ether alone. Preparations were tested for HA activity in dextrose-gelatin-Veronal (DGV) buffer solutions; 0.85% NaCl; Sorenson's phosphate-buffered saline, pH 7.2; and a diluent of 0.9% NaCl, 0.1% CaCl(2) (anhydrous), and 0.1% MgSO(4).7H(2)O. HA titers were consistently two- to fourfold higher in the saline with added Ca(++) and Mg(++) than in DGV. Hemagglutination-inhibition titers of paired human sera were the same in either diluent. It is suggested that the interaction between rubella HA antigen and the red cells of young (less than 1-day-old) chicks may be at least partially ion dependent and that titers are enhanced by increased quantities of divalent cations.

Animals↗
PubMed1982

Comparison of the latex agglutination test with the hemagglutination inhibition test, enzyme-linked immunosorbent assay, and neutralization test for detection of antibodies to rubella virus.

The ability of a rapid, latex agglutination test to diagnose rubella infection and to measure immune status was evaluated by comparison with the hemagglutination-inhibition (HAI) test, enzyme-linked immunosorbent assay (ELISA), and the neutralization (NT) test. The latex agglutination test accurately detected serological conversions in 74 pairs of sera representing 21 natural infections and 53 immunizations. The antibody levels of 276 sera from the general population were determined by latex agglutination, HAI, and ELISA. The correlation coefficients between the titers obtained by HAI and latex agglutination and by ELISA and latex agglutination were statistically significant. Results on 12 sera did not agree when measured by the three tests. These sera were included among the 196 specimens tested by NT. The correlation coefficient between NT and latex agglutination titers was statistically significant. There was one serum positive by latex agglutination but negative by NT, and five sera were negative by latex agglutination but had titers of 4 to 8 in the NT. The relative sensitivity of detecting antibody was greater by latex agglutination than by HAI. An additional 49 sera containing residual nonspecific hemagglutinin inhibitors were evaluated by latex agglutination and NT. The untreated sera showed no false positive reactions, and 36 of 39 NT positive sera were positive in the latex agglutination test.

Antibodies, Viral↗
PubMed1980

[Serotyping of bacteria of the genus Providencia using the indirect hemagglutination test and the indirect hemagglutination inhibition test].

The experiments with the collection of strains and diagnostic sera available in the USSR confirmed the data contained in the literature on the good prospects of using the indirect hemagglutination test for the serotyping of bacteria belonging to the genus Providencia. Certain differences were observed in cross reactions, revealed by the indirect hemagglutination test and by agglutination: the interrelations of serogroups O14 and O25, O23 and O25, O23 and O29, O29 and O45, O37 and O49, determined by means of the indirect hemagglutination test, could not be detected in the same sera by the slide and tube agglutination tests. For the first time the usefulness of aqueous-saline extracts of agar cultures in the indirect hemagglutination inhibition test to specify more precisely the interrelations between individual bacterial serogroups of the genus Providencia has been shown.

Hemagglutination Inhibition Tests↗