autoantibodies in le r3 anchisa srivipatana. antinuclear antibody (ana)
DESCRIPTION
ANA ANA assay identifies antibodies present in serum that bind to autoantigens present in the nuclei (or cytoplasm) of mammalian cells Many subtypes of ANAsTRANSCRIPT
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Autoantibodies in LER3 Anchisa Srivipatana
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Antinuclear antibody (ANA)
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ANA
•ANA assay identifies antibodies present in serum that bind to autoantigens present in the nuclei (or cytoplasm) of mammalian cells
•Many subtypes of ANAs
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Autoantibody associations of ACLE
•ACLE are those associated with SLE
•high-titer ANA, anti-dsDNA, anti-Sm, and hypocomplementemia
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Autoantibody associations of SCLE • anti-Ro/SS-A 70%–90%
• anti-La/SS-B 30%–50%• ANA 60%–80% • rheumatoid factor 33%• false-positive serologic tests for syphilis (VDRL
rapid plasma reagin) 7%–33%• anticardiolipin 10%–16%• antithyroid 18%–44%• anti-Sm 10%• anti-ds-DNA 10%• anti-U1 ribonucleoprotein 10%
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Autoantibody associations of DLE
• ANA are present in low titer in 30%–40%• Fewer than 5% have the higher ANA
levels that are characteristic of patients with overt SLE (>1:320)
• Antibodies to ssDNA, dsDNA are uncommon
• Ro/SS-A and La/SS-B autoantibodies are rare in patients with DLE
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ANA•Nucleated substrate: Human tumor cell
line such as Hep 2 cell
• Auto Ab are detected with a fluorochrome conjugated antiserum that is specific for human immunoglobulin (the aAb) that is bound to nuclei in the cell substrate
• The use of Hep 2 cells, only ~1–2% of SLE patients are ANA negative
• ANA in SLE patients: sensitivity 98% and specificity 90%
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ANA test•Indirect immunofluoresence
(Report pattern and titer)•Enzyme-linked
immunosorbent assay (ELISA)
•Crithidia luciliae test
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Indirect immunofluorescence•One of the most commonly used
tests for ANAs•Substrate: HEp-2 cell
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Stages of immunofluorescence for the detection of antinuclear antibodies• (1)HEp-2 cells are permeablised • (2)Incubated with a person's blood
serum • If the serum contains antibodies, they
will bind to antigens within the HEp-2 cell nucleus
• (3) These antibodies can be visualised by subsequent incubation with anti-human antibodies conjugated to a fluorescent molecule
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ANA patterns
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Immunofluorescence Patterns of ANA
Homogenous pattern
Peripheral pattern(Rim pattern)
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Speckled pattern
Nucleolar pattern
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Immunofluorescence Patterns of ANA
Centomeric pattern (Discrete speckled
pattern)
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Positive ANA in other AI-CTDs•Systemic sclerosis
90%•Sjogren’s syndrome
70% •Idiopathic inflammatory der
matomyopathies (DM/PM) 40–65%
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Homogeneous and speckled pattern
•Most laboratories report patterns•Commonly occur in healthy and
older individual•Clinically relevant ; High titer ≥1 :
160
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Peripheral pattern•Presence of autoAb to DNA,
including dsDNA
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Centromeric pattern•Antibodies binding to the
polypeptide components of chromosomal centromeres
•Associated primarily with the limited form of SSc
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Nucleolar pattern •Auto Ab binding to ribosomal RNA
processing molecules such as fibrillarin
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•The popular ELISA assays preferentially detect low-avidity anti dsDNA aAb that are also seen in patients who do not have SLE. It is recom mended that all positive anti dsDNA aAb ELISA results be confirmed by a second assay technique that detects high-avidity anti dsDNA aAb, such as the Farr radioimmunoassay or the Crithidia luciliae indirect immunofluorescence assay.
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Crithidia luciliae•Crithidia luciliae are haemoflaggellate
single celled protozoa•Used as a substrate in
immunofluorescence for the detection of anti-dsDNA antibodies
•Organelle known as the kinetoplast which is a large mitochondria with a network of interlocking circular dsDNA molecules
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Crithidia luciliae•After incubation with serum containing anti-dsDNA antibodies and fluorescent-labelled anti-human antibodies, the kinetoplast will fluoresce.
•The lack of other nuclear antigens in this organelle means that using C.luciliae as a substrate allows for the specific detection of anti-dsDNA antibodies
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Crithidia luciliae
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ELISA method
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ELISA method
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Anti Ro/SS A and Anti La/SS B aAb
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Anti Ro/SS A and anti La/SS B aAb
•AutoAb react with proteins in human cytoplasmic RNP (hYRNP) that are found in both the cytoplasm and nucleus
•“linked set” of autoantigens by present in the same RNP particles.
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Anti RNP aAb assays
•To measure anti Ro/SS A, anti La/SS B, anti U1RNP and anti Sm aAb
•Detect method : ELISA •ELISA is more sensitive but less
specific for detecting anti RNP aAb
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Anti Ro/SS A and anti La/SS B aAb
•Anti-Ro antibodies are specific to components of the Ro-RNP complex, comprising 45kDa, 52kDa, 54kDa and 60kDa proteins and RNA
•The 60kDa DNA/RNA binding protein and 52kDa T-cell regulatory protein are the best characterised antigens of anti-Ro antibodies
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Anti Ro/SS A and anti La/SS B aAb
•The La antigen is a 48kDa transcription termination factor of RNA polymerase III, which associates with the Ro-RNP complex
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Speckled Immunofluoresence staining pattern of anti-nuclear antibodies on HEp-20-10 cells. This staining pattern is seen with anti-Ro and anti-La antibodies
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Thank You