An Animal Model for Acute and Persistent Epstein-Barr Virus Infection-Reference-Cited by-同舟云学术

An Animal Model for Acute and Persistent Epstein-Barr Virus Infection

Published:1997-06-27 Issue:5321 Volume:276 Page:2030-2033
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Moghaddam Amir¹²³⁴,Rosenzweig Michael¹²³⁴,Lee-Parritz David¹²³⁴,Annis Bethany¹²³⁴,Johnson R. Paul¹²³⁴,Wang Fred¹²³⁴

Affiliation:

1. A. Moghaddam, B. Annis, F. Wang, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Avenue, Boston, MA 02115, USA.

2. M. Rosenzweig, Division of Immunology, New England Regional Primate Research Center, Harvard Medical School, 1 Pine Hill Drive, Southborough, MA 01172, USA.

3. D. Lee-Parritz, Division of Primate Resources, New England Regional Primate Research Center, Harvard Medical School, 1 Pine Hill Drive, Southborough, MA 01172, USA.

4. R. P. Johnson, Division of Immunology, New England Regional Primate Research Center, Harvard Medical School, 1 Pine Hill Drive, Southborough, MA 01172, USA, and AIDS Research Center and Infectious Disease Unit, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.

Abstract

Epstein-Barr virus (EBV) is a human lymphocryptovirus that causes infectious mononucleosis, persists asymptomatically for life in nearly all adults, and is associated with the development of B cell lymphomas and nasopharyngeal carcinomas. A highly similar rhesus lymphocryptovirus naturally endemic in rhesus monkeys was used to orally infect naı̈ve animals from a pathogen-free colony. This animal model reproduced key aspects of human EBV infection, including oral transmission, atypical lymphocytosis, lymphadenopathy, activation of CD23 + peripheral blood B cells, sustained serologic responses to lytic and latent EBV antigens, latent infection in the peripheral blood, and virus persistence in oropharyngeal secretions. This system may be useful for studying the pathogenesis, prevention, and treatment of EBV infection and associated oncogenesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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