Oligoclonal band

Proteins separated by SDS-PAGE, Coomassie brilliant blue staining

Oligoclonal bands (OCBs) are bands of immunoglobulins that are seen when a patient's blood serum, or cerebrospinal fluid (CSF) is analyzed. They are used in the diagnosis of various neurological and blood diseases. Oligoclonal bands are present in the CSF of more than 95% of patients with clinically definite multiple sclerosis.[1]

Two methods of analysis are possible: (a) protein electrophoresis, a method of analyzing the composition of fluids, also known as "SDS-PAGE (sodium dodecyl sulphate polyacrylamide gel electrophoresis)/Coomassie blue staining", and (b) the combination of isoelectric focusing/silver staining. The latter is more sensitive.[2]

For the analysis of cerebrospinal fluid, a sample is first collected via lumbar puncture (LP). Normally it is assumed that all the proteins that appear in the CSF, but are not present in the serum, are produced intrathecally (inside the central nervous system). Therefore, it is normal to subtract bands in serum from bands in CSF when investigating CNS diseases. A sample of blood serum is usually obtained from a clotted blood sample taken around the time of the LP.

Oligoclonal bands in multiple sclerosis

OCBs are especially important for multiple sclerosis (MS). In MS, normally only OCBs made of immunoglobulin G antibodies are considered, though sometimes other proteins can be taken into account, like lipid-specific immunoglobulin M.[3][4] The presence of these IgM OCBs is associated with a more severe course.[5]

Typically for an OCB analysis, the CSF is concentrated and the serum is diluted. After this dilution/concentration prealbumin appears as higher on CSF. Albumin is typically the dominant band on both fluids. Transferrin is another prominent protein on CSF column because its small molecular size easily increases its filtration in to CSF. CSF has a relatively higher concentration of prealbumin than does serum. As expected large molecular proteins are absent in CSF column. After all these bands are localized, OCBs should be assessed in the γ region which normally hosts small group of polyclonal immunoglobulins.[6]

New techniques like "capillary isoelectric focusing immunoassay" are able to detect IgG OCBs in more than 95% of multiple sclerosis patients.[7]

Even more than 12 OCBs can appear in MS.[8] Each one of them represent antibody proteins (or protein fragments) secreted by plasma cells, although why exactly these bands are present, and which proteins these bands represent, has not yet been fully elucidated. The target antigens for these antibodies are not easy to find because it requires to isolate a single kind of protein in each band, though new techniques are able to do so.[9]

In 40% of MS patients with OCBs, antibodies specific to the viruses HHV-6 and EBV have been found.[10]

HHV-6 specific OCBs have also been found in other demyelinating diseases.[11][12] A lytic protein of HHV-6A virus was identified as the target of HHV-6 specific oligoclonal bands.[13]

Though early theories assumed that the OCBs were somehow pathogenic autoantigens, recent research has shown that the IgG present in the OCBs are antibodies against debris, and therefore, OCBs seem to be just a secondary effect of MS.[14] Nevertheless, OCBs remain useful as a biomarker.

Diagnostic value in MS

Oligoclonal bands are an important indicator in the diagnosis of multiple sclerosis. Up to 95% of all patients with multiple sclerosis have permanently observable oligoclonal bands[15] at least for those with European ancestry.[16] The last available reports in 2017 were pointing to a sensitivity of 98% and specificity of 87% for differential diagnosis versus MS mimickers (specificity respect unselected population should be equal or higher).[17]

Other application for OCBs is as a tool to classify patients. It is known since long ago that OCB negative MS patients have a slower evolution. Some reports point that the underlying condition that causes the MS lesions in these patients is different. There are four pathological patterns of damage, and in the majority of patients with pattern II and III brain lesions oligoclonal bands are absent or only transiently present.[18]

Heterogeneity

It has been reported that oligoclonal bands are nearly absent in patients with pattern II and pattern III lesion types.[19]

Six groups of patients are usually separated, based on OCBs:[20]

  • type 1, no bands in CSF and serum;
  • type 2, oligoclonal IgG bands in CSF,
  • type 3, oligoclonal bands in CSF and serum with additional bands in CSF;
  • type 4, identical oligoclonal bands in CSF and serum,
  • type 5, monoclonal bands in CSF and serum,
  • type 6, presence of a single band limited to the CSF.

Type 2 and 3 indicate intrathecal synthesis, and the rest are considered as negative results (No MS).

Alternatives

The main importance of oligoclonal bands was to demonstrate the production of intrathecal immunoglobins (IgGs) for establishing a MS diagnosis. Currently alternative methods for detection of this intrathecal synthesis have been published, and therefore it has lost some of its importance in this area.

A specially interesting method are free light chains (FLC), specially the kappa-FLCs (kFLCs). Several authors have reported that the nephelometric and ELISA FLCs determination is comparable with OCBs as markers of IgG synthesis, and kFLCs behave even better than oligoclonal bands.[21]

Another alternative to oligoclonal bands for MS diagnosis is the MRZ-reaction (MRZR), a polyspecific antiviral immune response against the viruses of measles, rubella and zoster found in 1992.[22]

In some reports the MRZR showed a lower sensitivity than OCB (70% vs. 100%), but a higher specificity (92% vs. 69%) for MS.[22]

Bands in other diseases

The presence of one band (a monoclonal band) may be considered serious, such as lymphoproliferative disease, or may simply be normal—it must be interpreted in the context of each specific patient. More bands may reflect the presence of a disease.

Diseases associated

Oligoclonal bands may be found in:

References

  1. ^ Correale J, de los Milagros M, Molinas B (2002). "Oligoclonal bands and antibody responses in Multiple Sclerosis". Journal of Neurology. 249 (4): 375–389. doi:10.1007/s004150200026. PMID 11967640. S2CID 21523820.
  2. ^ Davenport RD, Keren DF (1988). "Oligoclonal bands in cerebrospinal fluids: significance of corresponding bands in serum for diagnosis of multiple sclerosis". Clinical Chemistry. 34 (4): 764–5. doi:10.1093/clinchem/34.4.764. PMID 3359616.
  3. ^ Álvarez-Cermeño JC, Muñoz-Negrete FJ, Costa-Frossard L, Sainz de la Maza S, Villar LM, Rebolleda G (2016). "Intrathecal lipid-specific oligoclonal IgM synthesis associates with retinal axonal loss in multiple sclerosis". Journal of the Neurological Sciences. 360: 41–44. doi:10.1016/j.jns.2015.11.030. PMID 26723970. S2CID 4724614.
  4. ^ Villar Luis M.; et al. (2015). "Lipid-specific immunoglobulin M bands in cerebrospinal fluid are associated with a reduced risk of developing progressive multifocal leukoencephalopathy during treatment with natalizumab". Annals of Neurology. 77 (3): 447–457. doi:10.1002/ana.24345. PMID 25581547. S2CID 20377417.
  5. ^ Ferraro D, et al. (2015). "Cerebrospinal fluid CXCL13 in clinically isolated syndrome patients: Association with oligoclonal IgM bands and prediction of Multiple Sclerosis diagnosis" (PDF). Neuroimmunology. 283: 64–69. doi:10.1016/j.jneuroim.2015.04.011. hdl:11380/1118697. PMID 26004159. S2CID 41252743.
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Community college in Oneida County, New York, U.S. This article uses bare URLs, which are uninformative and vulnerable to link rot. Please consider converting them to full citations to ensure the article remains verifiable and maintains a consistent citation style. Several templates and tools are available to assist in formatting, such as reFill (documentation) and Citation bot (documentation). (August 2022) (Learn how and when to remove this message) This article contains content that is wri...

 

Albert Gazier

Pour les articles homonymes, voir Gazier. Albert Gazier Fonctions Ministre de l'Information 17 mai 1958 – 1er juin 1958(15 jours) Président René Coty Président du Conseil Pierre Pflimlin Gouvernement Pflimlin Prédécesseur Robert Buron Successeur André Malraux 12 juillet 1950 – 11 août 1951(1 an et 30 jours) Président Vincent Auriol Président du Conseil René PlevenHenri Queuille Gouvernement Pleven IQueuille III Successeur Robert Buron Ministre des Affaires social...