» Articles » PMID: 6179155

A Synergistic Polyclonal Response to Dextran Sulphate and Lipopolysaccharide: Immunoglobulin Secretion and Cell Requirements

Overview
Journal Scand J Immunol
Date 1981 May 1
PMID 6179155
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The effects of the simultaneous addition of lipopolysaccharide (LPS) and dextran sulphate (DxS) were studied in a low-cell density culture system, which enables extensive cell proliferation and high immunoglobulin secretion. Using these two mitogens, a synergistic response was observed, with regard to both cell division and IgM secretion. However, only a very low IgG production could be detected. This was caused by the extensive cell proliferation, leading to suboptimal culture conditions. Thus, when the blasts were recultured at a lower density or when a lower initial cell concentration was used, a high IgG response was obtained. The synergistic response induced by LPS plus DxS was independent of T cells. Furthermore, no apparent need for phagocytic cells was found. Both the LPS- and the LPS plus DxS-induced activation led to a switch, preferentially to IgG2b and IgG3 secretion. This subclass pattern was not changed when the cultures were lacking functional T cells.

Citing Articles

The inflammatory infiltrate in the acute stage of the dextran sulphate sodium induced colitis: B cell response differs depending on the percentage of DSS used to induce it.

Stevceva L, Pavli P, Husband A, Doe W BMC Clin Pathol. 2001; 1(1):3.

PMID: 11580872 PMC: 57007. DOI: 10.1186/1472-6890-1-3.


Transforming growth factor beta 1 selectivity stimulates immunoglobulin G2b secretion by lipopolysaccharide-activated murine B cells.

McIntyre T, Klinman D, Rothman P, Lugo M, Dasch J, Mond J J Exp Med. 1993; 177(4):1031-7.

PMID: 8459202 PMC: 2190989. DOI: 10.1084/jem.177.4.1031.


Macrophage depletion decreases IgG anti-DNA in cultures from (NZB x NZW)F1 spleen cells by eliminating the main source of IL-6.

Alarcon-Riquelme M, Moller G, Fernandez C Clin Exp Immunol. 1993; 91(2):220-5.

PMID: 8428389 PMC: 1554691. DOI: 10.1111/j.1365-2249.1993.tb05886.x.