Evidence map›Paper›PMID 20421879›Full record

ArticleImmunology and cell biology2011

Memory CD8+ T cells from naturally acquired primary dengue virus infection are highly cross-reactive.

Heather Friberg, Lynne Burns, Marcia Woda, Siripen Kalayanarooj, Timothy P Endy, Henry A F Stephens, Sharone Green, Alan L Rothman, Anuja Mathew

Open access · greenAbstract read
In one paragraph

Article in Immunology and cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.4field-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

46 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. T Cell Responses During Dengue Infection.Current topics in microbiology and immunology · 2026
    Review
  6. Review
  7. Article
  8. Immune mechanisms in cancer patients that lead to poor outcomes of SARS-CoV-2 infection.Translational research : the journal of laboratory and clinical medicine · 2022
    Review
  9. Host immune response against DENV and ZIKV infections.Frontiers in cellular and infection microbiology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Japanese Encephalitis Vaccines.Current treatment options in infectious diseases · 2020
    Review
  16. Review
  17. Review
  18. Review
  19. A review of Dengvaxia®: development to deployment.Human vaccines & immunotherapeutics · 2019
    Review
  20. Review
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

9 authors at 4 institutions in 3 countries.

Heather FribergCenter for Infectious Disease and Vaccine Research, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Lynne Burns
Marcia Woda
Siripen Kalayanarooj
Timothy P Endy
Henry A F Stephens
Sharone Green
Alan L Rothman
Anuja Mathew
University of Massachusetts Chan Medical School · USArmed Forces Research Institute of Medical Science · THQueen Sirikit National Institute of Child Health · THUniversity College London · GB

Funding

VIRAL DETERMINANTS OF SEVERE DENGUE DISEASEP01AI034533 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ROTHMAN, ALAN L · 1994 to 2022
$42.0M
Technologies for Human Cellular ImmunologyU19AI057319 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CO, MARYDAWN T · 2003 to 2013
$34.4M
PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
NIAID NIH HHS P01 AI034533NIAID NIH HHS P01 AI34533NIAID NIH HHS U19 AI057319NIAID NIH HHS U19 AI57319NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

Cross-reactive memory T cells induced by primary infection with one of the four serotypes of dengue virus (DENV) are hypothesized to have an immunopathological function in secondary heterologous DENV infection. To define the T-cell response to heterologous serotypes, we isolated HLA-A(*)1101-restricted epitope-specific CD8(+) T-cell lines from primary DENV-immune donors. Cell lines exhibited marked cross-reactivity toward peptide variants representing the four DENV serotypes in tetramer binding and functional assays. Many clones responded similarly to homologous and heterologous serotypes with striking cross-reactivity between the DENV-1 and DENV-3 epitope variants. In vitro-stimulated T-cell lines consistently revealed a hierarchical induction of MIP-1β>degranulation>tumor necrosis factor α (TNFα)>interferon-γ (IFNγ), which depended on the concentration of agonistic peptide. Phosphoflow assays showed peptide dose-dependent phosphorylation of ERK1/2, which correlated with cytolysis, degranulation, and induction of TNFα and IFNγ, but not MIP-1β production. This is the first study to show significant DENV serotype-cross-reactivity of CD8(+) T cells after naturally acquired primary infection. We also show qualitatively different T-cell receptor signaling after stimulation with homologous and heterologous peptides. Our data support a model whereby the order of sequential DENV infections influences the immune response to secondary heterologous DENV infection, contributing to varying disease outcomes.

Indexed as

AdolescentAmino Acid SequenceAnimalsCD8-Positive T-LymphocytesCell LineCross ReactionsCytokinesDengueEpitopesExtracellular Signal-Regulated MAP KinasesHLA-A AntigensHumansMiceMice, Inbred BALB CReceptors, Antigen, T-CellSignal TransductionCytokinesEpitopesExtracellular Signal-Regulated MAP KinasesHLA-A AntigensReceptors, Antigen, T-Cell

Identifiers

PMID20421879
PMCPMC2929403
OpenAlexW1991139744

What OpenQuestion holds

Textmetadata
LicenceTDM
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.