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Sorted By Test Name - Mayo Medical Laboratories

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ROC<br />

5194<br />

ROM<br />

Reference Values:<br />

Negative (reported as positive, negative, or equivocal)<br />

Individuals who are immune to rubeola will have positive IgG test results by the EIA method and<br />

negative IgM test results by the IFA method. Those who are nonimmune will have negative test results by<br />

both methods. Recent infection with measles virus will be indicated by a positive IgM antibody result.<br />

The EIA test sensitivity is 96.9% and specificity is 100%. Similar performance characteristics are<br />

provided by the IFA test.<br />

Clinical References: 1. Liebert UG: Measles virus infections of the central nervous system.<br />

Intervirology 1997;40:176-184 2. Norrby E, Kristensson K: Measles virus in the brain. Brain Res Bull<br />

1997;44:213-220 3. Sable CA, Hayden FG: Orthomyxoviral and paramyxoviral infections in transplant<br />

patients. Infect Dis Clin North Am 1995;9:987-1003 4. Matsuzono Y, Narita M, Satake A, et al: Measles<br />

encephalomyelitis in a patient with a history of vaccination. Acta Paediatr Jpn 1995;37:374-376 5. Cremer<br />

NE, Devlin VL, Riggs JL, Hagens SJ. Anomalous antibody responses in viral infection: specific<br />

stimulation or polyclonal activation? J Clin Microbiol 1984;20:468-472 6. Gershon AA, Krugman S:<br />

Measles virus. In Diagnostic Procedures for Viral, Rickettsial and Chlamydial Infections. 5th edition.<br />

Edited by EH Lennette, NJ Schmidt. Washington, DC, American Public Health Association, Inc., 1979,<br />

pp 665-693<br />

Rubeola (Measles) Antibodies, IgG and IgM (Separate<br />

Determinations), Spinal Fluid<br />

Clinical Information: Measles is a serious and highly contagious disease which can be a leading<br />

cause of death where nutrition and sanitation are limited. Onset begins with cough, fever, and<br />

lymphadenopathy approximately 2 weeks after exposure. Diagnosis is usually made when the rash<br />

appears. Koplikâ€s spots may be seen earlier on the buccal mucosa. Complications of measles may<br />

develop in children who appear to have normal immune functions. Persistent infection of the central<br />

nervous system with measles virus is recognized to cause the disease subacute sclerosing panencephalitis<br />

(SSPE). SSPE is a rare, late complication of measles with an incidence of approximately 1 per 100,000<br />

cases. SSPE is a progressive, usually fatal disease that occurs most often in children between the ages of 5<br />

and 14. The onset is insidious and progressive. The incubation period from acute measles to onset of<br />

neurological symptoms varies from several months to many years. One of the most useful diagnostic tests<br />

involves the measurement of measles-specific antibodies in the cerebrospinal fluid (CSF) of patients with<br />

SSPE. Levels of antibody are significantly elevated in the CSF of SSPE patients compared to those<br />

without the disease.<br />

Useful For: Diagnosis of central nervous system infection with rubeola (measles) virus and/or subacute<br />

sclerosing panencephalitis<br />

Interpretation: Detection of organism-specific antibodies in the cerebrospinal fluid (CSF) may<br />

suggest central nervous system infection. However, these results are unable to distinguish between<br />

intrathecal antibodies and serum antibodies introduced into the CSF at the time of lumbar puncture or<br />

from a breakdown in the blood-brain barrier. The results should be interpreted with other laboratory and<br />

clinical data prior to a diagnosis of central nervous system infection Patients with subacute sclerosing<br />

panencephalitis have serum antibody titers which are 10 to 100 times higher than those seen in late<br />

convalescent-phase sera. More importantly, there is pronounced local production of oligoclonal measles<br />

virus antibodies in the central nervous system. Normals: -IgG:

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