Volume 93C, Issue 1-6 pp. 19-23
Full Access

ANTI-IMMUNOGLOBULINS IN EXPERIMENTAL STREPTOCOCCAL IMMUNIZATION; RELATION TO BACTERIAL GROWTH CONDITIONS AND Fc-RECEPTORS

LARISSA A. BUROVA

LARISSA A. BUROVA

Institute of Experimental Medicine, Academy of Medical Sciences of the USSR, Leningrad, USSR

Search for more papers by this author
POUL CHRISTENSEN

POUL CHRISTENSEN

Department of Medical Microbiology, University of Lund, Lund, Sweden

Search for more papers by this author
RUNE GRUBB

RUNE GRUBB

Department of Medical Microbiology, University of Lund, Lund, Sweden

Search for more papers by this author
CLAES SCHALEN

Corresponding Author

CLAES SCHALEN

Department of Medical Microbiology, University of Lund, Lund, Sweden

Department of Medical Microbiology, Sölvegatan 23, S-223 62 Lund, SwedenSearch for more papers by this author
MAJ-LIS SVENSSON

MAJ-LIS SVENSSON

Department of Medical Microbiology, University of Lund, Lund, Sweden

Search for more papers by this author
PETER P. BELTUKOV

PETER P. BELTUKOV

Institute of Experimental Medicine, Academy of Medical Sciences of the USSR, Leningrad, USSR

Search for more papers by this author
ARTEM A. TOTOLIAN

ARTEM A. TOTOLIAN

Institute of Experimental Medicine, Academy of Medical Sciences of the USSR, Leningrad, USSR

Search for more papers by this author
First published: November 1985
Citations: 4

Abstract

Heat-killed group A streptococci of types M12 and M22 were used for intravenous immunization of 60 rabbits. Presence of Fc-receptors binding monomeric IgG in M22 and their absence in M12 has been demonstrated previously. The strains were cultured in either Todd-Hewitt broth supplemented with 10% horse serum (TH-H) or in IsoVitaleX, a synthetic medium, supplemented with 10% autologous rabbit serum (IV-R). A mortality rate of 38% was noted in the first-mentioned group whereas no mortality was observed in the second group. Sera were examined for agglutination of red blood cells coated with either human or rabbit IgG. Antisera to strains cultured in TH-H regularly displayed anti-IgG antibodies reacting with human as well as rabbit IgG; anti-rabbit IgG titres of anti-M22 sera were significantly higher than those of anti-M12 sera. Antisera to strains grown in IV-R displayed high levels of antibodies reacting with human but not with rabbit IgG. The levels of anti-human IgG did not differ between anti-M12 and anti-M22 sera.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.