Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1980 Jun;11(6):573-8.
doi: 10.1128/jcm.11.6.573-578.1980.

Enzyme-linked immunosorbent assay for detection of Haemophilus influenzae type b antigen

Comparative Study

Enzyme-linked immunosorbent assay for detection of Haemophilus influenzae type b antigen

B L Wetherall et al. J Clin Microbiol. 1980 Jun.

Abstract

An enzyme-linked immunosorbent assay for the detection of Haemophilus influenzae type b antigen was developed. It was able to detect purified polyribose phosphate at concentrations of greater than or equal to 1 ng/ml in cerebrospinal fluid. This was 50 times more sensitive than counterimmunoelectrophoresis with the same antiserum. The sensitivity for polyribose phosphate in urine was similar, but that in serum was about 10 times less. Nonspecific reactions were observed with blood-stained cerebrospinal fluid and some sera. These were differentiated from true positive reactions by a blocking test with unconjugated immune serum. A wide range of organisms was tested for cross-reactivity in the assay. With the exception of a protein A-rich strain of Staphylococcus aureus, they gave absorbances of < 8% of that of the homologous system. In a series of five cases of proven H. influenzae type b meningitis, the sensitivity of the assay with cerebrospinal fluid was confirmed to be at least 2(5) times greater than that of counterimmunoelectrophoresis. The results indicate that the enzyme-linked immunosorbent assay is highly sensitive and specific in detecting H. influenzae type b antigen. The necessity to perform the blocking assay on all sera limits its usefulness for the examination of these specimens. However, it should prove valuable for the detection of the antigen in cerebrospinal fluid and urine.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Pediatr. 1976 Nov;89(5):773-5 - PubMed
    1. J Clin Pathol. 1976 Oct;29(10):873-9 - PubMed
    1. J Clin Invest. 1972 Jan;51(1):39-44 - PubMed
    1. J Lab Clin Med. 1973 May;81(5):770-7 - PubMed
    1. J Clin Microbiol. 1979 May;9(5):575-8 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources