Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1974 Aug;10(2):316-9.
doi: 10.1128/iai.10.2.316-319.1974.

Influence of hyperimmune immunoglobulin G on the physicochemical properties of the surface of Salmonella typhimurium 395 MS in relation to interaction with phagocytic cells

Influence of hyperimmune immunoglobulin G on the physicochemical properties of the surface of Salmonella typhimurium 395 MS in relation to interaction with phagocytic cells

O Stendahl et al. Infect Immun. 1974 Aug.

Abstract

Partition in an aqueous, two-polymer phase system containing dextran and polyethylene glycol was employed to investigate the physicochemical changes inflicted by the presence of immunoglobulin G (IgG) antibodies on the cell surface of a smooth strain of Salmonella typhimurium. Adding increasing amounts of anti-Salmonella IgG to the bacteria decreased the affinity for the polyethylene glycol-rich top phase, with a concomitant increase in in vivo clearance and in vitro phagocytosis by rabbit polymorphonuclear cells. Similarly, S --> R mutations in the same S. typhimurium strain decrease the affinity for the top phase and increase the liability to phagocytosis. The limiting antibody concentration to demonstrate increase of in vitro phagocytosis was approximately the same as that to produce a significant effect in the phase system, whereas lower concentrations were needed to increase the in vivo clearance. The results show that adsorption of IgG antibodies to bacteria brings about physicochemical changes of the cell surface which seem to promote the phagocytosis by polymorphonuclear cells and uptake in the reticuloendothelial system.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Clin Invest. 1974 Feb;53(2):536-43 - PubMed
    1. Nature. 1966 Apr 30;210(5035):496-8 - PubMed
    1. Z Naturforsch B. 1967 Jan;22(1):109 - PubMed
    1. Semin Hematol. 1968 Apr;5(2):134-55 - PubMed
    1. J Exp Med. 1968 Nov 1;128(5):991-1009 - PubMed

LinkOut - more resources