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Antinuclear Cytoplasmic Antibody

Editor: Narothama R. Aeddula Updated: 8/14/2023 9:11:22 PM

Introduction

The design of the human body is such that it can fight against infections and cancer cells and can kill them. An essential feature of the human immune system is recognizing and distinguishing between its cells (known as 'self') and foreign cells like bacteria and viruses (known as 'non-self'). Every cell has proteins related to their origin and functioning environment, which are called antigens, which serve to differentiate between self or non-self by the immune system. As a component of the immune system, antibodies or immunoglobulins are proteins produced by a type of immune cells called B Lymphocytes, which get converted into plasma cells eventually. These antibodies are mostly produced during exposure to infection or by binding to antigens, and their job is to neutralize or eliminate non-self-entities entering the body. Antibodies are also produced via vaccination by either exposure to killed antigens or direct inoculation of already formed antibodies in vitro.

The immune system's failure to recognize 'self' is called autoimmunity, in which the immune system attacks some tissues of the human body and destroys it. In autoimmunity, there is the formation of antibodies against self-antigens called autoantibodies. These autoantibodies form against one type of cell to which they bind and destroy.

Anti-neutrophil cytoplasmic antibodies are specific antibodies formed against cytoplasmic granules (antigens) of polymorphonuclear neutrophil granulocytes (PMNs).[1] These autoantibodies are present in ANCA-associated small-vessel vasculitides. The applied use of ANCA lab test, which detects ANCA autoantibodies, is used in the diagnosis of a few vasculitis diseases, mainly pauci-immune small vessel vasculitides granulomatosis with polyangiitis (GPA or Wegener granulomatosis), microscopic polyangiitis (MPA), and to lesser extent eosinophilic granulomatosis with polyangiitis (EGPA or Churg Strauss syndrome) and anti-GBM disease.[1][2]

Pathophysiology

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Pathophysiology

ANCA binds explicitly to two proteins in the cytoplasm of neutrophils in ANCA associated vasculitis, named proteinase-3 (PR3) and myeloperoxidase (MPO).[3] These patients have autoantibodies against PR3 (PR3-ANCA) or MPO (MPO-ANCA) at a time.[3] PR3-ANCA is more found explicitly in granulomatosis with polyangiitis (GPA or Wagner’s Granulomatosis) than others.[4] MPO-ANCA can be found in microscopic polyangiitis (MPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg Strauss Syndrome) more frequently than in GPA.[4]

Small vessel damage caused by ANCA occurs when these autoantibodies bind to granules in neutrophils, the mechanism of pathogenesis is given below[5][6]:

  • Neutrophils and monocytes activation by ANCA
  • Subsequent activation of the alternative complement pathway
  • Neutrophils migration through blood vessel walls and the release of inflammatory mediators
  • Release of chemoattractant and recruitment of more inflammatory mediators
  • Inflammation, apoptosis, necrosis, and damage to small blood vessel walls

Recently it has been discovered that few medications can cause drug-induced anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV). The drug-induced AAV is seen with propylthiouracil, hydralazine, and D-penicillamine.[7][8][9] Its pathogenesis is multifactorial. Drug-induced AAV is reversible after medication discontinuation, so it has a good prognosis.[7]

There are two following subtypes/patterns of ANCA[2][10]:

  1. c-ANCA (cytoplasmic pattern on IIF), which targets PR3 (proteinase 3) in neutrophilic cytoplasm
  2. p-ANCA (perinuclear pattern on IIF), which targets MPO (myeloperoxidase) in neutrophilic cytoplasm

ANCA lab testing shows which type of antibody is present, which then narrows down the differential diagnosis.

Specimen Requirements and Procedure

A blood sample is taken from a peripheral venous draw. A healthcare professional puts a rubber band around the arm and asks the patient to keep pumping fist for some time. Healthcare professional palpates the vein for confirmation and then applies alcohol swabs to clean the area. After it has dried up, the phlebotomist introduces a needle into the vein and collects a blood sample in a test tube or a vial. After collecting the sample, the band is removed, the pressure is applied over the puncture site, hemostasis is secured, and a bandage is applied. Complications of the procedure include mild tenderness, bruising, oozing of blood or infection at the puncture site.

Testing Procedures

After taking a blood sample, it undergoes analysis by two techniques[3]:

  1. Indirect immunofluorescence (IIF)
  2. Enzyme-linked immunosorbent assay (ELISA)

The indirect immunofluorescence (IIF) identifies ANCA by its staining patterns inside the cytoplasm of neutrophils[10]. In this technique, neutrophils are fixed via ethanol onto a slide, serum of blood sample is mixed on the slide with the neutrophils and ANCA, if present, in the sample attach to neutrophils on the slide. The slide is then treated with fluorochrome-stained antibodies which react with ANCA on the slide; this forms a fluorescence pattern that is visible via a microscope. As mentioned earlier, if ANCA staining is throughout the cytoplasm, it is called a c-ANCA pattern, mostly with PR3-ANCA. If staining is only around the nucleus, it is called p-ANCA (perinuclear pattern), which usually occurs with MPO-ANCA.[10] On the other hand, ELISA measures the level of MPO-ANCA or PR3-ANCA patterns in a blood sample.

Testing takes place in two steps. First indirect immunofluorescence (IIF) is done, which detects the presence or absence of these autoantibodies, and if the test comes positive, then it is followed by ELISA.[11] The International Consensus Statement on Testing and Reporting ANCA recommends using both techniques to detect ANCA in suspected patients.[12]

Interfering Factors

ANCA testing helps diagnose and monitor small vessel vasculitis, but it has some limitations too. There is a variant of ANCA called atypical ANCA, which is associated with drug-induced ANCA-associated vasculitis (AAV), inflammatory bowel disease, and rheumatoid arthritis.[13][14] ANCA positive rate is also higher in type 1 diabetes mellitus than in healthy individuals.[15]

Results, Reporting, and Critical Findings

Negative IIF result, i.e., ANCA is not detected: Normal.

Positive IIF result, i.e., ANCA is detected: Abnormal (In this case, the fluorescence pattern is also given to show whether c-ANCA or p-ANCA is present).

MPO Antibody (p-ANCA) Levels

  • >5.0 IU/ml = Positive
  • 3.5-5 IU/ml = Equivocal
  • <3.5 IU/ml = Negative

PR3 Antibody (c-ANCA) Levels

  • >3.0 IU/ml = Positive
  • 2-3.0 IU/ml = Equivocal
  • <2.0 IU/ml = Negative

Interpretation

Positive results for c-ANCA are mostly consistent with granulomatosis with polyangiitis (GPA or Wegener granulomatosis). Whereas positive results with p-ANCA mostly occur in microscopic polyangiitis (MPA) and eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss syndrome). Monitoring the titers of ANCAs are useful in monitoring the clinical course of diseases.

Clinical Significance

Positive ANCA lab results with clinical suspicion aids in diagnosing some small vessel vasculitis, including pauci-immune small vessel vasculitides granulomatosis with polyangiitis (GPA or Wegener granulomatosis), microscopic polyangiitis (MPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss syndrome) and anti-glomerular basement disease.[1][2] The reappearance of ANCA after the treatment of vasculitis can indicate a relapsing disease.[16][17]

References


[1]

Weiner M, Segelmark M. The clinical presentation and therapy of diseases related to anti-neutrophil cytoplasmic antibodies (ANCA). Autoimmunity reviews. 2016 Oct:15(10):978-82. doi: 10.1016/j.autrev.2016.07.016. Epub 2016 Jul 29     [PubMed PMID: 27481040]


[2]

Noël LH. [Antineutrophil cytoplasm antibodies (ANCA): description and immunopathological role]. Annales de medecine interne. 2000 May:151(3):178-83     [PubMed PMID: 10896969]


[3]

Silva de Souza AW. Autoantibodies in systemic vasculitis. Frontiers in immunology. 2015:6():184. doi: 10.3389/fimmu.2015.00184. Epub 2015 Apr 22     [PubMed PMID: 25954277]


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Yoshida M. [Antineutrophil cytoplasmic antibody(ANCA)]. Rinsho byori. The Japanese journal of clinical pathology. 2003 Jul:51(7):644-8     [PubMed PMID: 12924248]


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Jennette JC, Falk RJ. Pathogenesis of antineutrophil cytoplasmic autoantibody-mediated disease. Nature reviews. Rheumatology. 2014 Aug:10(8):463-73. doi: 10.1038/nrrheum.2014.103. Epub 2014 Jul 8     [PubMed PMID: 25003769]

Level 3 (low-level) evidence

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Jennette JC, Falk RJ. B cell-mediated pathogenesis of ANCA-mediated vasculitis. Seminars in immunopathology. 2014 May:36(3):327-38. doi: 10.1007/s00281-014-0431-y. Epub 2014 Apr 29     [PubMed PMID: 24777746]

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Gao Y, Zhao MH. Review article: Drug-induced anti-neutrophil cytoplasmic antibody-associated vasculitis. Nephrology (Carlton, Vic.). 2009 Feb:14(1):33-41. doi: 10.1111/j.1440-1797.2009.01100.x. Epub     [PubMed PMID: 19335842]

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[8]

Kumar B, Strouse J, Swee M, Lenert P, Suneja M. Hydralazine-associated vasculitis: Overlapping features of drug-induced lupus and vasculitis. Seminars in arthritis and rheumatism. 2018 Oct:48(2):283-287. doi: 10.1016/j.semarthrit.2018.01.005. Epub 2018 Jan 12     [PubMed PMID: 29519741]


[9]

Kang S, Cho MH, Hyun H, Kim JH, Ko JS, Kang HG, Cheong HI, Kim WS, Moon KC, Ha IS. A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome. Journal of Korean medical science. 2019 Jun 24:34(24):e173. doi: 10.3346/jkms.2019.34.e173. Epub 2019 Jun 24     [PubMed PMID: 31222986]

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[10]

Radice A, Sinico RA. Antineutrophil cytoplasmic antibodies (ANCA). Autoimmunity. 2005 Feb:38(1):93-103     [PubMed PMID: 15804710]


[11]

Sinico RA, Radice A. Antineutrophil cytoplasmic antibodies (ANCA) testing: detection methods and clinical application. Clinical and experimental rheumatology. 2014 May-Jun:32(3 Suppl 82):S112-7     [PubMed PMID: 24854381]


[12]

Savige J, Gillis D, Benson E, Davies D, Esnault V, Falk RJ, Hagen EC, Jayne D, Jennette JC, Paspaliaris B, Pollock W, Pusey C, Savage CO, Silvestrini R, van der Woude F, Wieslander J, Wiik A. International Consensus Statement on Testing and Reporting of Antineutrophil Cytoplasmic Antibodies (ANCA). American journal of clinical pathology. 1999 Apr:111(4):507-13     [PubMed PMID: 10191771]

Level 1 (high-level) evidence

[13]

Savige J, Davies D, Falk RJ, Jennette JC, Wiik A. Antineutrophil cytoplasmic antibodies and associated diseases: a review of the clinical and laboratory features. Kidney international. 2000 Mar:57(3):846-62     [PubMed PMID: 10720938]


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Bossuyt X. Serologic markers in inflammatory bowel disease. Clinical chemistry. 2006 Feb:52(2):171-81     [PubMed PMID: 16339302]


[15]

Omura T, Tamura Y, Kodera R, Oba K, Toyoshima K, Chiba Y, Sugihara T, Itabashi M, Shigemoto K, Araki A. Oldest-old type 1 diabetes patient receiving insulin pump treatment with positive myeloperoxidase-antineutrophil cytoplasmic antibody complication: A case report. Geriatrics & gerontology international. 2019 Sep:19(9):957-958. doi: 10.1111/ggi.13683. Epub     [PubMed PMID: 31490005]

Level 3 (low-level) evidence

[16]

Sinclair D, Stevens JM. Role of antineutrophil cytoplasmic antibodies and glomerular basement membrane antibodies in the diagnosis and monitoring of systemic vasculitides. Annals of clinical biochemistry. 2007 Sep:44(Pt 5):432-42     [PubMed PMID: 17761028]


[17]

Stegeman CA. Predictive value of antineutrophil cytoplasmic antibodies in small-vessel vasculitis: is the glass half full or half empty? The Journal of rheumatology. 2005 Nov:32(11):2075-7     [PubMed PMID: 16265681]