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


     
 


The Journal of Immunology, 1974, 113: 958-973.
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 Hamaoka, T.
Right arrow Articles by Benacerraf, B.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Hamaoka, T.
Right arrow Articles by Benacerraf, B.

Hapten-Specific IgE Antibody Responses in Mice

III. Establishment of Parameters for Generation of Helper T Cell Function Regulating the Primary and Secondary Responses of IgE and IgG B Lymphocytes1

Toshiyuki Hamaoka, Peter E. Newburger, David H. Katz and Baruj Benacerraf

From The Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115

Abstract

The present study was undertaken to carry out a detailed comparative analysis of the parameters most conducive to generation in inbred mice of antibody responses of the IgG vs IgE class, and more specifically, helper T cell function participating in antibody responses of these two classes. The data presented in this paper demonstrate the complex factors, i.e., the immunogenic strength, dose of antigen, and the nature of adjuvant vehicle employed for immunization, which determine the magnitude of helper function generated for either one or the other (or both) antibody classes. Although immunization regimens may be defined which result in some dissociation of IgE and IgG antibody responses, the overall impact of the evidence obtained indicates that the existence of distinct T cells for the regulation of these responses will be most difficult to demonstrate directly in the context of the numerous factors contributing to the generation of helper functions. Moreover, such a conclusion must be viewed with considerable caution since the data can equally be explained by differences in sensitivity of IgE and IgG B cells to the effects of the same activated T cells.

Footnotes

1 This investigation was supported by Grants AI-10630 and AI-09920 from the National Institutes of Health, United States Public Health Service.







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.