Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1960 Oct 31;112(5):953–961. doi: 10.1084/jem.112.5.953

ANAPHYLACTIC REACTIONS IN THE SKIN OF THE GUINEA PIG WITH HIGH AND LOW MOLECULAR WEIGHT ANTIBODIES AND GAMMA GLOBULINS

Zoltan Ovary 1, Hugh Fudenberg 1, Henry G Kunkel 1
PMCID: PMC2137296  PMID: 13731742

Abstract

High molecular weight (19S) γ-globulin produces passive cutaneous anaphylaxis (PCA) reactions with its specific antiserum only when it is used as intravenous antigen. Reversed PCA reactions cannot be produced when the 19S protein is injected intradermally in contradistinction to the results with 7S γ-globulin. Antibodies of the high molecular weight class, when injected intradermally, also failed to give PCA reactions following antigen injection. Heterophile antibodies from the sera of patients with infectious mononucleosis, demonstrated to be entirely of the 19S type, gave negative reactions, while 7S heterophile antibodies from guinea pig did give reactions following intravenous injection of sheep cells. Anti-B isoagglutinins of the 19S class failed to react, while those of the 7S class of similar titer gave clear reactions following the injection of B substance. Evidence was obtained that 19S antibodies were capable of inhibiting the PCA reactions obtained with the 7S type, indicating that interaction with antigen occurred. The failure to elicit PCA reactions appeared to be due to an inability to fix to guinea pig tissues in a manner similar to that known for 7S antibodies and γ-globulin.

Full Text

The Full Text of this article is available as a PDF (486.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BIER O. G., SIQUEIRA M. Passive reversed cutaneous anaphylaxis to protein antigens; preliminary report. Int Arch Allergy Appl Immunol. 1955;6(4-6):391–395. doi: 10.1159/000228196. [DOI] [PubMed] [Google Scholar]
  2. FRANKLIN E. C., KUNKEL H. G. Immunologic differences between the 19 S and 7 S components of normal human gamma-globulin. J Immunol. 1957 Jan;78(1):11–18. [PubMed] [Google Scholar]
  3. GREGERSEN M. I., RAWSON R. A. Blood volume. Physiol Rev. 1959 Apr;39(2):307–342. doi: 10.1152/physrev.1959.39.2.307. [DOI] [PubMed] [Google Scholar]
  4. OSLER A. G., HAWRISIAK M. M., OVARY Z., SIQUEIRA M., BIER O. G. Studies on the mechanism of hypersensitivity phenomena. II. The participation of complement in passive cutaneous anaphylaxis of the albino rat. J Exp Med. 1957 Dec 1;106(6):811–834. doi: 10.1084/jem.106.6.811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. OVARY Z., BIOZZI G. Passive sensitization of the skin of the guinea pig with human antibody. Int Arch Allergy Appl Immunol. 1954;5(3-4):241–245. doi: 10.1159/000228102. [DOI] [PubMed] [Google Scholar]
  6. OVARY Z. Immediate reactions in the skin of experimental animals provoked by antibody-antigen interaction. Prog Allergy. 1958;5:459–508. [PubMed] [Google Scholar]
  7. OVARY Z. Passive cutaneous anaphylaxis in the guinea pig: degree of reaction as a function of the quantity of antigen and antibody. Int Arch Allergy Appl Immunol. 1959;14(1-2):18–26. doi: 10.1159/000228504. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES