Evidence map›Paper›PMID 16877409›Full record

ArticleInvestigative ophthalmology & visual science2006

CD8 T cells mediate transient herpes stromal keratitis in CD4-deficient mice.

Andrew J Lepisto, Gregory M Frank, Min Xu, Patrick M Stuart, Robert L Hendricks

Open access · greenAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-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

34 citing papers in PubMed, 48 citations in OpenAlex.

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  12. Bolstering the Number and Function of HSV-1-Specific CD8Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  13. Article
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  17. Host immune cellular reactions in corneal neovascularization.International journal of ophthalmology · 2016
    Review
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  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Andrew J LepistoDepartment of Immunology, School of Medicine, University of Pittsburgh, Pennsylvania, USA.
Gregory M Frank
Min Xu
Patrick M Stuart
Robert L Hendricks
Ophthalmology Associates (United States) · USUniversity of Pennsylvania · US

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Andrew Ruzycki · 1985 to 2026
$18.4M
Virus Production and Manipulation of Protein/Gene Expression ModuleP30EY008098 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Ian A Sigal · 1989 to 2026
$17.8M
CYTOKINES AND ADHESION MOLECULES IN HSV KERATITISR01EY010359 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HENDRICKS, ROBERT L · 1994 to 2011
$4.9M
BIOPHYSICAL MECHANISMS OF SINGLE PHOTON DETECTIONR01EY011850 · NEI · UNIVERSITY OF WASHINGTON · PI RIEKE, FREDERICK M · 1997 to 2015
$3.5M
NEI NIH HHS P30 EY002687NEI NIH HHS P30 EY008098NEI NIH HHS P30-EY02687NEI NIH HHS P30-EY08098NEI NIH HHS R01 EY010359NEI NIH HHS R01 EY011850NEI NIH HHS R01 EY11850
6 · The paper itself

Abstract

purposeTo evaluate the role of CD4(+) T cells in the development of murine herpes stromal keratitis (HSK).

methodsThe corneas of wild-type (WT) BALB/c mice and three types of CD4-deficient BALB/c mice (CD4(-/-), CD4-depleted, CD4 and CD8 double-depleted) were infected with different doses of HSV-1 RE, and HSK incidence and severity were monitored. Corneal infiltrates were quantitatively and functionally assayed by flow cytometric analysis of individually digested diseased corneas and documented histologically.

resultsAt a relatively high infectious dose (1 x 10(5) pfu/cornea): (1) CD4-deficient and WT BALB/c mice had severe HSK with a similar incidence (80%-100%), whereas HSK did not develop in mice deficient in both CD4(+) and CD8(+) T cells; (2) neutrophils were the predominate leukocyte in the corneas of CD4-deficient and WT mice; (3) the corneas of WT mice had activated, HSV-1-specific CD4(+) T cells, but few if any CD8(+) T cells; (4) the corneas of CD4-deficient mice had activated, HSV-1-specific CD8(+) T cells; and (5) HSK in CD4-deficient mice was transient, showing loss of CD8(+) T cells at 2 to 3 weeks after infection (pi) followed by a loss of neutrophils. At a relatively low infectious dose of HSV-1 (10(3) pfu/cornea) severe HSK developed in 80% to 90% of WT mice, but in only 30% to 40% of CD4-deficient mice.

conclusionsCD4(+) T cells preferentially mediate HSK, but, in their absence, a high infectious dose of HSV-1 can induce histologically similar but transient HSK that is mediated by CD8(+) T cells.

Indexed as

AnimalsBone Marrow CellsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCorneal StromaDendritic CellsFemaleFlow CytometryHerpesvirus 1, HumanInterferon-gammaKeratitis, HerpeticLymphocyte ActivationLymphocyte DepletionMiceMice, Inbred BALB CMice, KnockoutInterferon-gamma

Identifiers

PMID16877409
PMCPMC2366973
OpenAlexW2021989975

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.