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Key points

  • Laboratory testing can help distinguish whether someone is susceptible to EBV infection or has a recent or past infection.
  • Healthcare providers can test for antibodies to specific EBV-associated antigens.
  • Monospot test is not recommended for general use.
This photomicrograph depicts leukemia cells that contain Epstein-Barr virus using an FA staining technique.

Overview

Epstein-Barr virus (EBV)also known as human herpesvirus 4is a gamma herpes virus that occurs only in humans. Laboratory testing can help distinguish whether someone is susceptible to EBV infection or has a recent or past infection.

EBV antibody tests are not usually needed to diagnose infectious mononucleosis. Howeverspecific antibody tests may be needed to for people who:

  • Do not have a typical case of infectious mononucleosis.
  • Have other illnesses that can be caused by EBV infection.

Types of tests

Viral capsid antigen (VCA)

Anti-VCA IgM appears early in EBV infection and usually disappears within four to six weeks.

Anti-VCA IgG appears in the acute phase of EBV infectionpeaks at 2 to 4 weeks after onsetdeclines slightly then persists for the rest of a person's life.

Early antigen (EA)

Anti-EA IgG appears in the acute phase of illness and generally falls to undetectable levels after three to six months. In many peopledetection of antibody to EA is a sign of active infection. However20% of healthy people may have antibodies against EA for years.

EBV nuclear antigen (EBNA)

Antibody to EBNA (determined by the standard immunofluorescent test) is not seen in the acute phase of EBV infection. Insteadit slowly appears 2 to 4 months after onset of symptoms and persists for the rest of a person’s life. Other EBNA enzyme immunoassays may report false positive results.

Monospot test

The Monospot test is not recommended for general use. The antibodies detected by Monospot can be caused by conditions other than infectious mononucleosis.

Moreoverstudies have shown that the Monospot produces both false positive and false negative results. For examplethe heterophile antibodies detected by Monospot are often not present in children with infectious mononucleosis.

At bestthe Monospot test may indicate that a person has a typical case of infectious mononucleosis but does not confirm the presence of EBV infection.

Virus detection

If patient is ill for more than 6 months‎

Symptoms of infectious mononucleosis generally resolve within 4 weeks. If a person is ill for more than 6 months and does not have a laboratory-confirmed diagnosis of EBV infectionother causes of chronic illness or chronic fatigue syndrome should be considered.

How to interpret tests

The interpretation of EBV antibody tests requires familiarity with these tests and access to the patient's clinical information.

Susceptibility to infection

People are considered susceptible to EBV infection if they do not have antibodies to the VCA.

Primary (new or recent) infection

People are considered to have a primary EBV infection if they have anti-VCA IgM but do not have antibody to EBNA.

Other results that strongly suggest a primary infection are a high or rising level of anti-VCA IgG and no antibody to EBNA after at least 4 weeks of illness. Resolution of the illness may occur before the diagnostic antibody levels appear.

In rare casespeople with active EBV infections may not have detectable EBV-specific antibodies.

Past infection

The presence of antibodies to both VCA and EBNA suggests past infection (from several months to years earlier).

Since over 90% of adults have been infected with EBVmost adults will show antibodies to EBV from infection years earlier. High or elevated antibody levels may be present for years and are not diagnostic of recent infection.

Recent vs. past infections

Testing paired acute-phase and convalescent-phase serum samples is not useful to distinguish between recent and past EBV infections. In most casesthe antibody response occurs rapidly during primary EBV infection. The clinical findings of infectious mononucleosis occur in conjunction with the appearance of IgG and IgM anti-VCA antibodies. Howeverthe antibody pattern is not stable before symptoms appear.