» Articles » PMID: 4544246

Induction of IgG by Lipid A in the Newborn Mouse

Overview
Journal J Exp Med
Date 1974 Mar 1
PMID 4544246
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

IgG of paternal allotype first becomes detectable in the serum of (BALB/c x C57BL/6)F(1) mice between day 12 and 14 after birth and reaches adult levels at an age of 5 wk. Since in mice there is a transfer of maternal IgG molecules through the placenta and via milk, F(1) heterozygous at the allotype locus were used and the concentrations of IgG with paternal allotype were measured. This was done by a sensitive method capable of detecting IgG concentrations as low as 5 x 10(-4) of normal adult serum levels. It is based on the quantitative inhibition of allotype-specific facilitation of hemolysis. When lipid A or Salmonella bacteria were injected into neonatal mice, a stimulation of IgG synthesis was observed. Thus IgG levels were enhanced 10-30-fold compared to the nontreated mice. No increase in IgG levels was obtained in adult mice after treatment with lipid A. Whether the newborns were injected at birth, on day 2, 4, or 7, IgG was first demonstrable in the treated mice at an age of 6-11 days. The increase in IgG levels was not paralleled by a demonstrable antibody activity against lipid A, SRBC, and LPS. Thus the bulk of newly induced IgG is probably a statistical distribution of different specificities.

Citing Articles

Immunological responses of mice to native protoplasmic polysaccharide and lipopolysaccharide: functional separation of the two signals required to stimulate a secondary antibody response.

Von Eschen K, Rudbach J J Exp Med. 1974; 140(6):1604-14.

PMID: 4610079 PMC: 2139752. DOI: 10.1084/jem.140.6.1604.


Induction of IgG in young nude mice by lipid A or thymus grafts.

Kolb C, Di Pauli R, Weiler E J Exp Med. 1976; 144(4):1031-6.

PMID: 978133 PMC: 2190427. DOI: 10.1084/jem.144.4.1031.


Comparative studies on the actions of antigen and polyclonal B-cell activator in differentiation and proliferation of B-cells and B memory cells.

Nakashima I, Nagase F, Yokochi T, Kojima T, Ohta M, Kato N Immunology. 1976; 31(4):649-58.

PMID: 789231 PMC: 1445356.


Functional maturation of neonatal spleen cells.

Immunology. 1979; 36(3):527-32.

PMID: 312262 PMC: 1457571.

References
1.
Weiler E, Melletz E . Facilitation of immune hemolysis by an interaction between red cell-sensitizing antibody and gamma-globulin allotype antibody. Proc Natl Acad Sci U S A. 1965; 54(5):1310-7. PMC: 219894. DOI: 10.1073/pnas.54.5.1310. View

2.
Watson J, Trenkner E, Cohn M . The use of bacterial lipopolysaccharides to show that two signals are required for the induction of antibody synthesis. J Exp Med. 1973; 138(3):699-714. PMC: 2139420. DOI: 10.1084/jem.138.3.699. View

3.
Kindred B, Weiler E . Recessive inheritance of rapid anti-allotype antibody production. J Immunol. 1971; 107(2):389-93. View

4.
Galanos C, LUDERITZ O, Westphal O . Preparation and properties of antisera against the lipid-A component of bacterial lipopolysaccharides. Eur J Biochem. 1971; 24(1):116-22. DOI: 10.1111/j.1432-1033.1971.tb19661.x. View

5.
Weiler E, Weiler I, Sprenger R, Dittrich B . Analysis of antibody populations to oligo-alanine determinants. L. An antibody assay by one-hit sensitization of red cells. Eur J Immunol. 1971; 1(5):377-84. DOI: 10.1002/eji.1830010515. View