Evidence map›Paper›PMID 16586361›Full record

ArticleThe Journal of infectious diseases2006

Anti-severe acute respiratory syndrome coronavirus immune responses: the role played by V gamma 9V delta 2 T cells.

Fabrizio Poccia, Chiara Agrati, Concetta Castilletti, Licia Bordi, Cristiana Gioia, Douglas Horejsh, Giuseppe Ippolito, Paul K S Chan, David S C Hui, Joseph J Y Sung and 2 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

67 citing papers in PubMed, 88 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Association of prior treatment with nitrogen-containing bisphosphonates on outcomes of COVID-19 positive patients.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
    Article
  10. Human Challenge Studies with Coronaviruses Old and New.Current topics in microbiology and immunology · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Global patterns of antigen receptor repertoire disruption across adaptive immune compartments in COVID-19.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Review
  20. Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

12 authors at 4 institutions in 4 countries.

Fabrizio PocciaUnit of Cellular Immunology, National Institute for Infectious Diseases Lazzaro Spallanzani, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy. poccia@inmi.it
Chiara Agrati
Concetta Castilletti
Licia Bordi
Cristiana Gioia
Douglas Horejsh
Giuseppe Ippolito
Paul K S Chan
David S C Hui
Joseph J Y Sung
Maria Rosaria Capobianchi
Miroslav Malkovsky
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITUniversity of Hong Kong · HKDepartment of Health · CNUniversity of Wisconsin–Madison · US

Funding

THERAPEUTIC VACCINATION FOR IMMUNODEFICIENCY VIRUSESR01AI048401 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI MALKOVSKY, MIROSLAV · 2000 to 2004
$1.6M
NIAID NIH HHS R01 AI048401NIAID NIH HHS R01AI48401
6 · The paper itself

Abstract

Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus (SARS-CoV) strain. Analyses of T cell repertoires in health care workers who survived SARS-CoV infection during the 2003 outbreak revealed that their effector memory V gamma 9V delta 2 T cell populations were selectively expanded ~3 months after the onset of disease. No such expansion of their alpha beta T cell pools was detected. The expansion of the V gamma 9V delta 2 T cell population was associated with higher anti-SARS-CoV immunoglobulin G titers. In addition, in vitro experiments demonstrated that stimulated V gamma 9V delta 2 T cells display an interferon- gamma -dependent anti-SARS-CoV activity and are able to directly kill SARS-CoV-infected target cells. These findings are compatible with the possibility that V gamma 9V delta 2 T cells play a protective role during SARS.

Indexed as

Immunologic MemoryAdultAntibodies, ViralFemaleHumansImmunoglobulin GMaleReceptors, Antigen, T-Cell, gamma-deltaSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusT-Lymphocyte SubsetsAntibodies, ViralImmunoglobulin GReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID16586361
PMCPMC7110256
OpenAlexW2079821054

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.