Selective Lack of Antibody to a Component of Eb Nuclear Antigen in Patients with Chronic Active Epstein-Barr Virus Infection

George Miller, Elizabeth Grogan, David Rowe, Cliona Rooney, Lee Heston, Robin Eastman, Warren Andiman, James Niederman, Gilbert Lenoir, Werner Henle, John Sullivan, Robert Schooley, Jaak Vossen, Stephen Strauss, Thomas Issekutz

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

64 Citas (Scopus)

Resumen

The sera of 12 patients with presumed chronic active Epstein-Barr virus (EBV) infection lacked antibody to a component of the Epstein-Barr nuclear antigen (EBNA) complex encoded by the BamHI K fragment of viral DNA. This anomaly, detected in ∼18% of sera obtained from patients with a diagnosis of “chronic mononucleosis, “ was more often found in patients with severe disease (∼32%) who had objective clinical findings and markedly elevated antibody titers to EBV replicative antigens than in those patients with the “fatigue syndrome” (10%). The lack of antibody to the K nuclear antigen is specific because most of those who did not have antibody to the K antigen made antibody to other latent nuclear (EBNA 2) antigens or nuclear early antigens. Such patients are thus able to lyse immortalized cells, release nuclear products, and present them to the immune system. Three hypotheses are suggested to explain the lack of antibody to the K antigen: A viral mutation, a failure of immune recognition, or lack of in vivo expression of the antigen due to extensive viral replication. Lack of antibody to one component of EBNA may serve as an objective serological marker for certain patients with chronic EBV infection.

Idioma originalEnglish
Páginas (desde-hasta)26-35
Número de páginas10
PublicaciónJournal of Infectious Diseases
Volumen156
N.º1
DOI
EstadoPublished - jul. 1987
Publicado de forma externa

Nota bibliográfica

Funding Information:
Received for publication 20 October 1986, and in revised form 28 January 1987. This work was supported by grants AI-14741 and AI-22959 from the National Institute of Allergy and Infectious Diseases. We thank D. M. Horstmann for criticisms and suggestions, K. Papov for secretarial assistance, and J. F. Jones and J. Gallin for referring patients. Please address requests for reprints to Dr. George Miller, Division of Infectious Diseases, Department of Pediatrics, Yale University School of Medicine, P.O. Box 3333, New Haven, Connecticut 06510-8064.

ASJC Scopus Subject Areas

  • Immunology and Allergy
  • Infectious Diseases

PubMed: MeSH publication types

  • Journal Article
  • Research Support, U.S. Gov't, P.H.S.

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