The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


The Journal of Immunology, 1974, 112: 804-811.
Copyright © 1974 by The American Association of Immunologists, Inc.

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Terres, G.
Right arrow Articles by Stoner, R. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Terres, G.
Right arrow Articles by Stoner, R. D.

Carrier-Specific Enhancement of the Immune Response Using Antigen-Antibody Complexes1

Geronimo Terres2, Gail S. Habicht3 and Richard D. Stoner4

From the Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111 and the Division of Microbiology, Medical Research Center, Brookhaven National Laboratory, Upton, New York 11973

Abstract

Antigen-antibody complexes formed at equivalence and injected into adult mice sensitize the mice so that a markedly enhanced antibody response is obtained following an injection of soluble antigen 3 days after the complex injection. The serologic specificity of the enhanced response is determined by the antigen injected on day 3; thus, rabbit anti-dog serum albumin (DSA) in complex with DSA sensitizes the mouse so that when human serum albumin (HSA) is injected on day 3 an enhanced antibody response to determinants unique to HSA is obtained. The antigen injected on day 3 must be related to the antigen in complex in order to produce an enhanced response; tetanus toxoid given on day 3 following injection of DSA-anti-DSA did not stimulate an anti-tetanus response. A mechanism is proposed in which the day 3 antigen-specific bursal-equivalent (B) cells produce an enhanced antibody response as a result of interaction with an increased number of carrier-specific thymus-derived (T) cells which have been stimulated to proliferate by the antigen-antibody complex; in this scheme, the albumin determinants which stimulate T cells to proliferate differ from those which stimulate antibody formation, i.e., B cells.

Footnotes

1 This research was supported by United States Public Health Service Grant AI-09643-0 ALY and the United States Atomic Energy Commission.

2 Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111.

3 Department of Microbiology, State University of New York at Stony Brook, Stony Brook, New York 11790.

4 Division of Pathology, Medical Research Center, Brookhaven National Laboratory, Upton, Long Island, New York 11973.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1974 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1974 by The American Association of Immunologists, Inc. All rights reserved.