The in vivo stability of antibody
- Creators
- Garvey, Justine S.
- Campbell, Dan H.
Abstract
Our previous studies, concerned largely with antigen retention and the characterization of antigen in tissues, led us to suspect that some antibody, like antigen, may be stabilized in tissue sites (1). The purpose of the present investigation was to study further, such antibody which appeared to be bound with antigen and perhaps normal tissue constituents. The investigation was carried out in the following manner: rabbits were first immunized by a series of intravenous injections of antigen and at the height of precipitin production they were fed S35-labelled yeast cells. Newly produced antibody, like the other plasma proteins, became readily labelled with S35 amino acids within a few hours. After varying lengths of time, when circulating antibody had declined, antigen was again injected. Serum samples were then taken at various intervals and the specific activity of antibody was measured as soon as antibody reappeared in the circulation. The specific activity of antibody was measured in the antigen-antibody precipitates obtained, both in the period when the antibody had been allowed to decline and also after antigen had been reinjected to induce an anamnestic response. A comparison of antibody-specific activity provided evidence that there was a release of antibody which had been made at the time of S35 feeding and stored in some stabilized form in tissues. The results are discussed with respect to the anamnestic response and the retention of antigen in tissues.
Additional Information
© 1959, by The Rockefeller Institute. (Received for publication, April 24, 1959) The authors wish to express their appreciation for the very capable assistance of Mr. Bror Clark, Miss Rebecca Kent, and Mrs. Carla McNeill and the suggestions given by various members of the immunochemistry group. This work was supported by the National Institutes of Health and The Rockefeller Foundation. Contribution 2455 from the Division of Chemistry and Chemical Engineering, The California Institute of Technology, PasadenaAttached Files
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Additional details
- PMCID
- PMC2137007
- Eprint ID
- 4414
- Resolver ID
- CaltechAUTHORS:GARjem59
- NIH
- Rockefeller Foundation
- Created
-
2006-08-22Created from EPrint's datestamp field
- Updated
-
2021-11-08Created from EPrint's last_modified field
- Other Numbering System Name
- Caltech Division of Chemistry and Chemical Engineering
- Other Numbering System Identifier
- 2455