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From the Institute of Pathology, Western Reserve University, and the University Hospitals, Cheveland, Ohio
Abstract
A method for the titration of human complement is described.
The existence of at least four components in human complement, similar to, though not entirely identical with the components of guinea-pig complement, is established. Methods are given for the preparation of human complements lacking respectively in C'1, C'2, C'3 and C'4, and for the reactivation of these.
A method is given for the separation of human complement into two individually inactive fractions which are fully active upon recombination. This separation is achieved by dialysis of human serum against a phosphate buffer of ionic strength 0.02 and pH = 5.4. The two fractions obtained correspond functionally to the end-piece and mid-piece of guinea-pig complement.
It was found that C'3 is the only component which is effectively mutually substitutive in human and guinea-pig complement systems.
C'1 of cow and sheep sera were found effective in replacing human C'1.
The fortification of human complement by both guinea-pig and human specifically inactivated complements was attempted. Human "pH = 5.4 µ 0.02 supernate" was found effective in fortification of human complement; guinea-pig C'3, and to a lesser degree C'2, were found to be involved in the fortification of human complement by guinea-pig specifically inactivated complements.
Footnotes
1 Aided by a grant from the Commonwealth Fund.
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