Detection of Soluble Immune Complexes by the Technique of Antibody-Dependent Cell-Mediated Cytotoxicity Inhibition in Glomerulonephritis

2015 ◽  
pp. 134-149
Author(s):  
O. Meyer
Keyword(s):  
Immune Complexes ◽  
Dependent Cell ◽  
Soluble Immune Complexes

Isoelectric focusing analysis of soluble immune complexes bound to Protein A-sepharose

1981 ◽  
Vol 111 (2) ◽  
pp. 336-342 ◽  
Author(s):  
Bert W. Maidment ◽  
Lawrence D. Papsidero ◽  
Marie Gamarra ◽  
Takuma Nemoto ◽  
T.Ming Chu
Keyword(s):  
Isoelectric Focusing ◽  
Immune Complexes ◽  
Protein A ◽  
Soluble Immune Complexes

Uptake of Intravenously Administered Soluble Immune Complexes by Type I Alveolar Cells and Macrophages in Mice

1985 ◽  
Vol 78 (1) ◽  
pp. 108-111
Author(s):  
Y. Kanayama ◽  
K. Amatsu ◽  
N. Negoro ◽  
T. Takeda ◽  
T. Inoue
Keyword(s):  
Immune Complexes ◽  
Type I ◽  
Alveolar Cells ◽  
Soluble Immune Complexes

scholarly journals Activation of human platelets by immune complexes prepared with cationized human IgG

Blood ◽  
1993 ◽  
Vol 82 (10) ◽  
pp. 3045-3051
Author(s):  
M Schattner ◽  
M Lazzari ◽  
AS Trevani ◽  
E Malchiodi ◽  
AC Kempfer ◽  
...  
Keyword(s):  
Platelet Aggregation ◽  
Platelet Activation ◽  
Immune Complexes ◽  
Platelet Rich Plasma ◽  
Human Platelets ◽  
Human Igg ◽  
Experimental Conditions ◽  
Induce Platelet Aggregation ◽  
Soluble Immune Complexes ◽  
High Concentrations

The present study shows that the ability of soluble immune complexes (IC), prepared with human IgG and rabbit IgG antibodies against human IgG, to trigger platelet activation was markedly higher for IC prepared with cationized human IgG (catIC) compared with those prepared with untreated human IgG (cIC). CatIC induced platelet aggregation and adenosine triphosphate release in washed platelets (WP), gel-filtered platelets (GFP), or platelet-rich plasma (PRP) at physiologic concentrations of platelets (3 x 10(8)/mL) and at low concentrations of catIC (1 to 30 micrograms/mL). On the contrary, under similar experimental conditions, cIC did not induce aggregation in PRP, WP, or GFP. Low aggregation responses were only observed using high concentrations of both WP (9 x 10(8)/mL) and cIC (500 micrograms/mL). Interestingly, catIC were also able to induce platelet activation under nonaggregating conditions, as evidenced by P-selectin expression. Cationized human IgG alone did not induce platelet aggregation in PRP but triggered either WP or GFP aggregation. However, the concentration needed to induce these responses, was about eightfold higher than those required for catIC. The responses induced either by catIC or cationized human IgG were completely inhibited by treatment with heparin, dextran sulphate, EDTA, prostaglandin E1, or IV3, a monoclonal antibody against the receptor II for the Fc portion of IgG (Fc gamma RII). The data presented in this study suggest that IgG charge constitutes a critical property that conditions the ability of IC to trigger platelet activation.

scholarly journals Immunohistochemical detection of Fc receptor. I. Light microscopic demonstration of Fc receptor by using soluble immune complexes of peroxidase-antiperoxidase immunoglobulin G.

1977 ◽  
Vol 25 (4) ◽  
pp. 252-258 ◽  
Author(s):  
G Itoh ◽  
S Miura ◽  
I Suzuki
Keyword(s):  
Cell Surface ◽  
Immunoglobulin G ◽  
Immune Complexes ◽  
Surface Characterization ◽  
Fc Receptor ◽  
Frozen Sections ◽  
Microscopic Demonstration ◽  
Lymph Node Cells ◽  
Soluble Immune Complexes ◽  
And Control

The mouse mesenteric lymph node cells (in the cell suspension and frozen sections) were incubated in the soluble immune complexes of peroxidase-antiperoxidase immunoglobulin G. After being washed, they were reacted with diaminobenzidine tetrahydrochloride. Light microscopically brown-colored granules were observed on the cell surface of a proportion of small lymphocytes. In frozen sections, a proportion of small lymphocytes were stained dark brown on the cell surface. Characterization and control experiments suggest that the binding of peroxidase-antiperoxidase immunoglobulin G to the cell surface is mediated by Fc receptor. Peroxidase-antiperoxidase immunoglobulin G, therefore, can be used as in indicator of Fc receptor.

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