Evidence map›Paper›PMID 15113901›Full record

ArticleJournal of virology2004

Acute infection with Epstein-Barr virus targets and overwhelms the peripheral memory B-cell compartment with resting, latently infected cells.

Donna Hochberg, Tatyana Souza, Michelle Catalina, John L Sullivan, Katherine Luzuriaga, David A Thorley-Lawson

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 175 citations in OpenAlex.

  1. Exploring the effect of vitamin DMultiple sclerosis (Houndmills, Basingstoke, England) · 2018
    Trial
  2. Review
  3. Review
  4. Epstein-Barr Virus in Multiple Sclerosis: Past, Present, and Future.Neurology(R) neuroimmunology & neuroinflammation · 2025
    Review
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  8. Article
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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Donna HochbergDepartment of Pathology, Jaharis Building, Tufts University School of Medicine, 150 Harrison Avenue, Boston, MA 02111, USA.
Tatyana Souza
Michelle Catalina
John L Sullivan
Katherine Luzuriaga
David A Thorley-Lawson
Tufts University · USUniversity of Massachusetts Chan Medical School · US

Funding

Tetramer CoreP01AI049320 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KONZ, RICHARD FREDERICK · 2001 to 2016
$22.3M
UMASS MEDICAL CENTER FOR AIDS RESEARCHP30AI042845 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SCHIFFER, CELIA A. · 1998 to 2012
$13.0M
HOST IMMUNITY TO EBV INFECTION IN VITRO AND IN VIVOR01AI018757 · NIAID · TUFTS UNIVERSITY BOSTON · PI POLTORAK, ALEXANDER · 1985 to 2017
$6.7M
EPSTEIN BARR VIRUS LATENCYR01CA065883 · NCI · TUFTS UNIVERSITY BOSTON · PI THORLEY-LAWSON, DAVID A. · 1995 to 2014
$4.3M
NCI NIH HHS CA 65883NCI NIH HHS R01 CA065883NIAID NIH HHS AI 18757NIAID NIH HHS AI 42845NIAID NIH HHS AI 49320NIAID NIH HHS P01 AI049320NIAID NIH HHS P30 AI042845NIAID NIH HHS R01 AI018757
6 · The paper itself

Abstract

In this paper we demonstrate that during acute infection with Epstein-Barr virus (EBV), the peripheral blood fills up with latently infected, resting memory B cells to the point where up to 50% of all the memory cells may carry EBV. Despite this massive invasion of the memory compartment, the virus remains tightly restricted to memory cells, such that, in one donor, fewer than 1 in 10(4) infected cells were found in the naive compartment. We conclude that, even during acute infection, EBV persistence is tightly regulated. This result confirms the prediction that during the early phase of infection, before cellular immunity is effective, there is nothing to prevent amplification of the viral cycle of infection, differentiation, and reactivation, causing the peripheral memory compartment to fill up with latently infected cells. Subsequently, there is a rapid decline in infected cells for the first few weeks that approximates the decay in the cytotoxic-T-cell responses to viral replicative antigens. This phase is followed by a slower decline that, even by 1 year, had not reached a steady state. Therefore, EBV may approach but never reach a stable equilibrium.

Indexed as

Immunologic MemoryVirus LatencyAcute DiseaseAdolescentAdultB-LymphocytesHerpesvirus 4, HumanHumansImmunophenotypingInfectious MononucleosisT-Lymphocytes, CytotoxicVirus Replication

Identifiers

PMID15113901
PMCPMC400374
OpenAlexW2081021502

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.