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The biological activity of soluble antigen-antibody complexes: II. Physical properties of soluble complexes having skin-irritating activity

Ishizaka, Kimishige and Ishizaka, Teruko and Campbell, Dan H. (1959) The biological activity of soluble antigen-antibody complexes: II. Physical properties of soluble complexes having skin-irritating activity. Journal of Experimental Medicine, 109 (2). pp. 127-143. ISSN 0022-1007. PMCID PMC2136941. https://resolver.caltech.edu/CaltechAUTHORS:ISHjem59

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Abstract

Previous work by Germuth and McKinnon (1), Trapani et al. (2), and ourselves (3) has established the fact that soluble antigen-antibody complexes formed in excess antigen can, (a) induce symptoms similar to anaphylaxis, (b) cause contraction of isolated smooth muscle from normal guinea pigs, and (c) increase the permeability of skin capillaries in a manner similar to that obtained in passive cutaneous anaphylaxis. These findings immediately raise many questions as to the fundamental mechanisms involved. For example, is the free antigen playing some role; is the toxicity dependent upon some change in the molecular structure of either antigen or antibody upon combination; is the complex itself toxic without any change in the molecular structure of the components; is the antigen-antibody ratio important; and, is complement involved? The work reported here involves a study of the possible role of free antigen and the nature of the complex. Some study was also made of untreated and decomplemented antiserums and, although there was no difference, this cannot rule out the possible participation of the test animal's (guinea pig's) own complement.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1084/jem.109.2.127DOIArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/pmc2136941/PubMed CentralArticle
Additional Information:© 1959, by The Rockefeller Institute. (Received for publication, September 24, 1958) This work was supported in part by a grant from the National Institute of Allergy and Infectious Diseases and in part by The Rockefeller Foundation. The authors wish to acknowledge the helpful advice and criticisms of Doctors D. W. Talmage, S. J. Singer, I. L. Trapani, and W. E. Vannier, and the technical assistance of Mr. Bror Clark. Contribution No. 2402 from the Division of Chemistry and Chemical Engineering, The California Institute of Technology, Pasadena
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Rockefeller FoundationUNSPECIFIED
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Caltech Division of Chemistry and Chemical Engineering2402
Issue or Number:2
PubMed Central ID:PMC2136941
Record Number:CaltechAUTHORS:ISHjem59
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:ISHjem59
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:4411
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:22 Aug 2006
Last Modified:08 Jul 2020 21:09

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