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The Journal of Immunology, 1969, 102: 269-271.
Copyright © 1969 by The American Association of Immunologists, Inc.

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The Fixation of Guinea Pig Complement by {gamma}1 and {gamma}2 Immunoglobulins1

Abraham G. Osler2, Benedito Oliveira2, Hyun S. Shin3 and Ann L. Sandberg2

From the Department of Medical Immunology, The Public Health Research Institute of the City of New York, and the Department of Microbiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland

Abstract

Several years ago the 7 S guinea pig immunoglobulins were separated into two well-defined electrophoretic classes: the slowly migrating {gamma}2 and the more rapid {gamma}1 (1–3). This achievement led to further studies which demonstrated that the ability to activate the complement (C') sequence was confined to {gamma}2 immunoglobulins. These antibodies failed to mediate passive cutaneous anaphylaxis (PCA) in the guinea pig. In contrast, the {gamma}1 immunoglobulins were capable of eliciting PCA reactions despite their purported deficiency in C'-fixing potency.

We have re-investigated this question and have confirmed all the previous findings excepting the C'-fixing properties of {gamma}1 type antibodies. These immunoglobulins do interact with guinea pig C' components, but probably by a different pathway.

Hartley strain guinea pigs were immunized with highly substituted dinitrophenylated bovine {gamma} globulin (4) emulsified in complete Freund's adjuvant as described in (5). Initially, 250 µg of antigen were injected into each of the four toepads.

Footnotes

Support for this investigation was provided, in part, by the National Science Foundation. Grant GB-1120; The American Cancer Society, Inc., Grant T-257; The National Institute of Allergy and Infectious Diseases of the United States Public Health Service, Grant AI-03151; and the Office of The Surgeon General, Department of the Army, under the auspices of the Commission on Immunization of the Armed Forces Epidemiological Board, Contract DA-49-193-MD-2468.

2 Department of Medical Immunology, The Public Health Research Institute of New York, N. Y.

3 Department of Microbiology, The Johns Hopkins University School of Medicine, Baltimore, Md.







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