Evidence map›Paper›PMID 22665800›Full record

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

Perforin-dependent CD4+ T-cell cytotoxicity contributes to control a murine poxvirus infection.

Min Fang, Nicholas A Siciliano, Adam R Hersperger, Felicia Roscoe, Angela Hu, Xueying Ma, Ahamed R Shamsedeen, Laurence C Eisenlohr, Luis J Sigal

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 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

66 citing papers in PubMed, 88 citations in OpenAlex.

  1. Review
  2. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
  3. Article
  4. Review
  5. EomesoderminImmunity · 2025
    Article
  6. IL-21-dependent Ly6CCell death discovery · 2025
    Article
  7. Osteoblast-CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Article
  9. Review
  10. Role of lamin A/C on dendritic cell function in antiviral immunity.Cellular and molecular life sciences : CMLS · 2024
    Article
  11. The roles of CD4Molecular therapy. Nucleic acids · 2024
    Article
  12. Cytotoxic CD4+ T Cells Are Induced during Infection with Chlamydia trachomatis.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  13. Natural Immunomodulatory Agents as a Complementary Therapy for Poxviruses.Advances in experimental medicine and biology · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cytotoxic CD4Frontiers in immunology · 2023
    Review
  20. Review

6 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

9 authors at 2 institutions in 1 country.

Min FangImmune Cell Development and Host Defense Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Nicholas A Siciliano
Adam R Hersperger
Felicia Roscoe
Angela Hu
Xueying Ma
Ahamed R Shamsedeen
Laurence C Eisenlohr
Luis J Sigal
Fox Chase Cancer Center · USThomas Jefferson University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHARNITA M. ZEIGLER-JOHNSON · 1985 to 2026
$138.8M
The innate Immune Response to Mousepox at the Site - Associated ProjectU19AI083008 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI NORBURY, CHRISTOPHER C · 2009 to 2013
$9.6M
Orthropoxvirus Pathogenesis and VaccinesR01AI065544 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2006 to 2016
$5.7M
MHC Class I Antigen Presentation in Viral InfectionsR01AI048849 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI SIGAL, LUIS J · 2001 to 2011
$3.8M
NCI NIH HHS P30 CA006927NCI NIH HHS P30CA006927NIAID NIH HHS 5U19AI083008NIAID NIH HHS R01 AI048849NIAID NIH HHS R01AI048849NIAID NIH HHS R01 AI065544NIAID NIH HHS R01AI065544NIAID NIH HHS U19 AI083008
6 · The paper itself

Abstract

CD4(+) T cells are generally regarded as helpers and regulators of the immune response. Although cytolytic CD4(+) T cells have been described, whether those generated during the course of a viral infection play a role in virus control remains unknown. Here we show that during acute infection with ectromelia virus, the mouse homolog of the human virus of smallpox, large numbers of CD4(+) T cells in the draining lymph node and liver of resistant mice have a cytotoxic phenotype. We also show that these cells kill targets in vivo in a perforin-dependent manner and that mice with specific deficiency of perforin in CD4(+) T cells have impaired virus control. Thus, perforin-dependent CD4(+) T-cell killing of infected cells is an important mechanism of antiviral defense.

Indexed as

Cytotoxicity, ImmunologicAnimalsCD4-Positive T-LymphocytesEctromelia virusMajor Histocompatibility ComplexMicePerforinPerforin

Identifiers

PMID22665800
PMCPMC3382508
OpenAlexW1990782514

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.