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


     
 


The Journal of Immunology, 1961, 86: 146-150.
Copyright © 1961 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 Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ovary, Z.
Right arrow Articles by Karush, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ovary, Z.
Right arrow Articles by Karush, F.

Studies on the Immunologic Mechanism of Anaphylaxis1

II. SENSITIZING AND COMBINING CAPACITY IN VIVO OF FRACTIONS SEPARATED FROM PAPAIN DIGESTS OF ANTIHAPTEN ANTIBODY

Zoltan Ovary and Fred Karush

From the Department of Pathology, New York University, School of Medicine, New York City, New York and the Department of Pediatrics (Children's Hospital of Philadelphia), University of Pennsylvania, School of Medicine, Philadelphia, Pennsylvania

Abstract

The fractions obtained from purified rabbit antihapten antibody by papain digestion, which contain the antibody combining site (ADDS or ADS-I), were unable to sensitize the skin of the guinea pig for PCA or RPCA reactions. These fractions, however, when mixed with the intact antibody specifically inhibited the latter from producing PCA reactions showing that they can combine in vivo with the antigen. From a kinetic study it was concluded that these fractions diffuse away faster from the injection site than does the intact antibody. These fractions showed a precipitation line in agar double diffusion with horse-anti-rabbit {gamma}-globulin. The fraction without antibody combining site (ADDP) can produce good RPCA reactions. It was concluded that the failure of ADDS and ADS-I to produce PCA or RPCA reactions is due to their inability to be "fixed" to the guinea pig tissues and that this "fixation" site is present on ADDP.

Footnotes

1 These studies were aided by Research Grant E-3075 from the National Institute of Allergy and Infectious Diseases and H-869 from the National Heart Institute of the National Institutes of Health, United States Public Health Service.




This article has been cited by other articles:


Home page
ScienceHome page
N. E. Cremer, J. L. Riggs, E. H. Lennette, and F. W. Jensen
Nonspecific Binding of Complement by Digestion Fragments from Antiviral Gamma Globulin
Science, July 2, 1965; 149(3679): 84 - 85.
[Abstract] [PDF]


Home page
ScienceHome page
W. D. Terry and J. L. Fahey
Subclasses of Human ggr2-Globulin Based on Differences in the Heavy Polypeptide Chains
Science, October 16, 1964; 146(3642): 400 - 401.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1961 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1961 by The American Association of Immunologists, Inc. All rights reserved.