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. 1981 May;13(5):888-90.
doi: 10.1128/jcm.13.5.888-890.1981.

Choice and specificity of complement in complement fixation assay

Choice and specificity of complement in complement fixation assay

J Sethi et al. J Clin Microbiol. 1981 May.

Abstract

This study examines the relative activity of various complement sources in a variety of antigen-antibody (Ag-Ab) complement fixation assay systems. Studied were Ag-Ab systems of cytomegalovirus, adenovirus, Pneumococcus, Coccidiodes, and guinea pig kidney. Ab titers in each system were determined by microcomplement fixation assay using two batches of titrated rabbit, monkey, cat, dog, human cord, human adult, and guinea pig sera as complement sources. Assay sensitivity and Ab titers proved to be strongly related to the complement sources. There was considerable variation in the ability of Ag-Ab complexes to bind the complement of each of the species tested. Guinea pig, rabbit, and monkey sera gave comparable titers in four of the five Ag-Ab systems tested. Cat serum complement was able to detect anti-adenovirus and anti-Pneumococcus reactivity only. Human adult, human cord, and dog sera exhibited anti-complementary activity. The study emphasizes the importance of complement source in determining both the specificity and sensitivity of complement fixation assays in a given Ag-Ab system.

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References

    1. Nouv Rev Fr Hematol. 1968 Nov-Dec;8(6):864-8 - PubMed
    1. Nature. 1970 Mar 21;225(5238):1137-8 - PubMed
    1. Science. 1973 Aug 3;181(4098):440-2 - PubMed
    1. J Immunol. 1962 Mar;88:320-9 - PubMed
    1. N Engl J Med. 1974 Nov 21;291(21):1103-7 - PubMed

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