Introduction
Autoimmune diseases
Autoantibodies - Introduction
Autoantibodies - Determination
 
Autoantibodies
Rheumatoid Factor
Antinuclear Antibodies (ANA)
Specific Antibodies
Anti-neutrophil Cytoplasmic Antibodies
(ANCA)
Anti-phospholipid Antibodies
Anti-mitochondrial Antibodies (AMA)
Anti-endothelial Cell Antibodies (AECA)
Anti CCP antibodies
Antibodies against DNases
 
Quality Assurance
 
Reference ranges
 
Algorithm
ANA and incidence of diseases
Proposed stepwise diagnosis scheme
Positive Immunoflourescence -
Nucleoplasmic
Positive Immunoflourescence - Nucleolar
Positive Immunoflourescence -
Cytoplasmic
Type of autoimmune diseases
Conditions associated with antinuclear
antibodies (ANA)
 
Slide show
 
References
 
Collaborators
Antinuclear Antibodies (ANA) - Clinical significance


Diseases and autoantibodies associated with HEP-2 patterns
HEP-2 positivity is found in many diseases but also in some physiological conditions (Table 10). Care should always be taken when interpreting positive results in patients. Elderly, especially females (41) and pregnant women frequently have ANA (42), albeit in rather low titer, as may patients with tumors, chronic infections and many other diseases. Autoantibodies may also appear months or years before overt manifestations of an autoimmune disease. Whilst the presence of autoantibodies are of great diagnostic importance, results have to be interpreted only in the context of the clinical information (42).

Currently, the determination of ANA is widely used as screening procedure for autoimmune diseases such as SLE, MCTD, Sjögren’s syndrome, RA, polymyositis, scleroderma, dermatomyositis and CREST syndrome (Calcinosis, Raynaud, Esophagus, Sclerodactylia, Telangiectasia).
The presence of positive ANA in patient sera is presumptive evidence of underlying autoimmune diseases, but it is not itself considered as diagnostic. However, absence of ANA may rule out a particular diagnosis (28). The observation that many autoantibodies appear before the clinical expression of disease suggests that they are not epiphenomena.

1) Physiologic changes in the concentration of ANA-factor
2) Pathologic changes in the concentration Antinuclear Antibodies (ANA)
a) Increased Antinuclear Antibodies (ANA) in:
Acquired hemolytic anemia (non-specific)
Anaplastic carcinomas or lymphomas (non-specific)
Atypical pneumonia (non-specific)
Dermatomyositis (specific)
Hepatic or biliary cirrhosis
Infectious Hepatitis (non-specific)
Leprosy (non-specific)
Malaria (non-specific)
Mixed connective tissue disease (specific)
Mononucleosis (non-specific)
Periaerteritis nodosa (non-specific)
Rheumatoid arthritis (non-specific)
Scleroderma (specific)
Sjörgen’s syndrome (specific)
SLE (specific)
Tuberculosis (non-specific)