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


     
 


The Journal of Immunology, 1979, 123: 2709-2715.
Copyright © 1979 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 Kishimoto, T.
Right arrow Articles by Yamamura, Y.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Kishimoto, T.
Right arrow Articles by Yamamura, Y.

Regulation of Antibody Response in Different Immunoglobulin Classes

VI. Selective Suppression of IgE Response by Administration of Antigen-Conjugated Muramylpeptides1

Tadamitsu Kishimoto, Yoshikatsu Hirai2, Kenji Nakanishi, Ichiro Azuma3, Atsuo Nagamatsu4 and Yuichi Yamamura

From the Third Department of Internal Medicine, Osaka University Medical School, Fukushima-ku, Osaka, Japan

Abstract

The suppressive effect of antigen-conjugated muramylpeptides or 6-O-mycoloyl muramylpeptides selectively on the induction of IgE antibody response was demonstrated. Preadministration of DNP-mycoloyl muramylpeptides completely inhibited the induction of the anti-DNP IgE antibody response with DNP-ovalbumin (DNP-OA). The selective suppression of the IgE response was due to the induction of DNP-specific suppressor T cells by DNP-mycoloyl muramylpeptides, and the suppressor cells were shown to be radiosensitive. Preadministration of OA-conjugated muramylpeptides partially inhibited the primary and secondary induction of an anti-OA IgE antibody response. The suppressor effect was also due to the induction of OA-specific suppressor T cells. Application of allergen-conjugated muramylpeptides as therapeutic agents in human allergic diseases was suggested.

Footnotes

1 This work was supported by a Grant-in-Aid for immunologic research from the Ministry of Education, Science and Culture, Japan.

2 Present address: The Department of Biology, Brandeis University, Waltham, Massachusetts 02154.

3 Present address: The Institute of Immunological Science, Hokkaido University, Sapporo, Japan.

4 Present Address: The Department of Biochemistry, Fukuoka University School of Pharmaceutical Science, Fukuoka, Japan.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1979 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1979 by The American Association of Immunologists, Inc. All rights reserved.