scholarly journals Proceedings: Relationship between antinuclear antibodies, DNA binding capacity, and electroprecipitation, serum complement level, and the presence of soluble complexes in systemic lupus erythematosus and rheumatoid arthritis.

1975 ◽  
Vol 34 (5) ◽  
pp. 469-469 ◽  
Author(s):  
G D Johnson ◽  
I I Onyewotu ◽  
E J Holborrow
1970 ◽  
Vol 28 (1) ◽  
pp. 59-62
Author(s):  
H Rahman ◽  
A Begum ◽  
RR Roy ◽  
R Siddique ◽  
K Alam ◽  
...  

Systemic lupus erythematosus (SLE) is very rare and difficult to diagnose before 5 years of age. We are reporting a case of SLE at 2.5- year who presented with recurrent episodes of fever, haematuria , proteinuria and rash . Diagnosis of SLE was confirmed by reduced serum complement level and positive anti double stranded DNA (anti ds DNA). Class IV histological type of Lupus nephritis was evaluated by renal biopsy DOI: 10.3329/jbcps.v28i1.4647 J Bangladesh Coll Phys Surg 2010; 28: 59-62


1974 ◽  
Vol 19 (4) ◽  
pp. 171-175 ◽  
Author(s):  
J. Webb ◽  
K. Whaley ◽  
P. Lee

The native DNA binding assay has been employed to study antibodies to native DNA in patients with systemic lupus erythematosus and other connective tissue diseases. DNA binding values exceeding 30 per cent almost invariably confirm the diagnosis of active systemic lupus erythematosus. The DNA-antigen binding capacity of lupus sera appear to provide more information than the DNA binding assay alone, in assessing response to therapy and prognosis in this disease. The standard immunofluorescence antinuclear factor test should be used as a screening procedure where possible, and the DNA binding assay done on sera that are positive in titres of 1 in 256 or greater.


Author(s):  
Francis R. Comerford ◽  
Alan S. Cohen

Mice of the inbred NZB strain develop a spontaneous disease characterized by autoimmune hemolytic anemia, positive lupus erythematosus cell tests and antinuclear antibodies and nephritis. This disease is analogous to human systemic lupus erythematosus. In ultrastructural studies of the glomerular lesion in NZB mice, intraglomerular dense deposits in mesangial, subepithelial and subendothelial locations were described. In common with the findings in many examples of human and experimental nephritis, including many cases of human lupus nephritis, these deposits were amorphous or slightly granular in appearance with no definable substructure.We have recently observed structured deposits in the glomeruli of NZB mice. They were uncommon and were found in older animals with severe glomerular lesions by morphologic criteria. They were seen most commonly as extracellular elements in subendothelial and mesangial regions. The deposits ranged up to 3 microns in greatest dimension and were often adjacent to deposits of lipid-like round particles of 30 to 250 millimicrons in diameter and with amorphous dense deposits.


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