Evidence map›Paper›PMID 22778413›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

A Plasmodium-encoded cytokine suppresses T-cell immunity during malaria.

Tiffany Sun, Thomas Holowka, Yan Song, Swen Zierow, Lin Leng, Yibang Chen, Huabao Xiong, Jason Griffith, Mehdi Nouraie, Philip E Thuma and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

45 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Frontiers in immunology · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. CD4Malaria journal · 2022
    Article
  15. Host-parasite interactions duringFrontiers in immunology · 2022
    Review
  16. Suppression of Plasmodium MIF-CD74 signaling protects against severe malaria.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  17. Review
  18. Article
  19. Recombinant DBL2β-PfEMP1 of the IndonesianJournal of Taibah University Medical Sciences · 2021
    Article
  20. Frontiers in immunology · 2021
    Article
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

15 authors at 4 institutions in 2 countries.

Tiffany SunDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Thomas Holowka
Yan Song
Swen Zierow
Lin Leng
Yibang Chen
Huabao Xiong
Jason Griffith
Mehdi Nouraie
Philip E Thuma
Elias Lolis
Chris J Janse
Victor R Gordeuk
Kevin Augustijn
Richard Bucala
Yale University · USHoward University · USIcahn School of Medicine at Mount Sinai · USLeiden University · NL

Funding

STRUCTURAL/FUNCTIONAL CHARACTERIZATION OF AMINOGLYCOSIDEG12RR003048 · NCRR · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 1985 to 2011
$19.0M
MIF AND THE HOST RESPONSE TO INFECTIONR01AI042310 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 1998 to 2013
$4.3M
Inflammatory Suppression of Adaptive Immunity by Plasmodium MIFR01AI110452 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2014 to 2023
$4.2M
Training in Parasitology and Vector BiologyT32AI007404 · NIAID · YALE UNIVERSITY · PI TSCHUDI, CHRISTIAN · 1991 to 2017
$3.8M
Suppression of Erythropoiesis in Malaria InfectionR01AI051306 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2004 to 2008
$1.5M
NCRR NIH HHS G12 RR003048NIAID NIH HHS AI 2R01-042310-12NIAID NIH HHS AI 5R01-51306-05NIAID NIH HHS R01 AI042310NIAID NIH HHS R01 AI110452NIAID NIH HHS T32 AI007404PHS HHS 5732A1007404-20
6 · The paper itself

Abstract

The inability to acquire protective immunity against Plasmodia is the chief obstacle to malaria control, and inadequate T-cell responses may facilitate persistent blood-stage infection. Malaria is characterized by a highly inflammatory cytokine milieu, and the lack of effective protection against infection suggests that memory T cells are not adequately formed or maintained. Using a genetically targeted strain of Plasmodium berghei, we observed that the Plasmodium ortholog of macrophage migration inhibitory factor enhanced inflammatory cytokine production and also induced antigen-experienced CD4 T cells to develop into short-lived effector cells rather than memory precursor cells. The short-lived effector CD4 T cells were more susceptible to Bcl-2-associated apoptosis, resulting in decreased CD4 T-cell recall responses against challenge infections. These findings indicate that Plasmodia actively interfere with the development of immunological memory and may account for the evolutionary conservation of parasite macrophage migration inhibitory factor orthologs.

Indexed as

AnimalsApoptosisCD4-Positive T-LymphocytesCytokinesEvolution, MolecularHumansImmunologic MemoryMalaria, FalciparumMiceMice, Inbred BALB CPlasmodium bergheiPlasmodium falciparumProto-Oncogene Proteins c-bcl-2Protozoan ProteinsCytokinesProto-Oncogene Proteins c-bcl-2Protozoan Proteins

Identifiers

PMID22778413
PMCPMC3411961
OpenAlexW2160891320

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.