Evidence map›Paper›PMID 24519420›Full record

ArticleInvestigative ophthalmology & visual science2014

In vivo downregulation of innate and adaptive immune responses in corneal allograft rejection by HC-HA/PTX3 complex purified from amniotic membrane.

Hua He, Yaohong Tan, Stephanie Duffort, Victor L Perez, Scheffer C G Tseng

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

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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.

Hua HeTissueTech, Inc., Miami, Florida.
Yaohong Tan
Stephanie Duffort
Victor L Perez
Scheffer C G Tseng
University of Miami · USOcular Surface Center · US

Funding

Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Victor L Perez · 2004 to 2026
$12.2M
VITAMIN A AND CONJUNCTIVAL TRANSDIFFERENTIATIONR01EY006819 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TSENG, SCHEFFER CG · 1986 to 2020
$6.7M
Chemokines and T Cell Recruitment in High Risk Corneal Allograft RejectionR01EY018624 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PEREZ, VICTOR L · 2009 to 2013
$2.2M
Anti-angiogenesis of HC-HA Covalent Complex and PTX3 Purified from Fetal MembraneR43EY021045 · NEI · TISSUETECH, INC. · PI TSENG, SCHEFFER CG · 2011 to 2011
$240k
ANTI-SCARRING AND ANTI-INFLAMMATORY EFFECTS OF AMNIOTIC MEMBRANE EXTRACTSR43EY017497 · NEI · TISSUETECH, INC. · PI TSENG, SCHEFFER C G · 2006 to 2006
$113k
NEI NIH HHS P30 EY014801NEI NIH HHS R01 EY006819NEI NIH HHS R01 EY018624NEI NIH HHS R43 EY017497NEI NIH HHS R43 EY021045
6 · The paper itself

Abstract

purposeHeavy chain-hyaluronic acid (HC-HA)/PTX3 purified from human amniotic membrane (AM) was previously observed to suppress inflammatory responses in vitro. We now examine whether HC-HA/PTX3 is able to exert a similar effect in vivo, using murine models for keratitis and corneal allograft rejection.

methodsThe in vitro effect of HC-HA/PTX3 was tested using OTII ovalbumin (OVA) transgenic, purified CD4(+) T cells, or IFN-γ/lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Cytokine production was measured by ELISA, while cell surface markers and cell proliferation were determined by flow cytometry. In vivo effects of HC-HA/PTX3 were analyzed by quantifying the recruitment of enhanced green fluorescence-labeled macrophages and by measuring the expression of arginase 1 (Arg-1), IL-10, and IL-12 in LPS-induced keratitis in the macrophage Fas-induced apoptosis (Mafia) mouse. The effect of corneal allograft survival in a complete major histocompatibility complex (MHC) mismatched mouse model was assessed by grading corneal opacification.

resultsIn vitro studies demonstrated that HC-HA/PTX3 significantly enhanced the expansion of FOXP3 T cells and suppressed cell proliferation and protein expression of IFN-γ, IL-2, CD25, and CD69 in activated CD4(+) T cells. Furthermore, immobilized HC-HA/PTX3 significantly upregulated IL-10 gene expression but downregulated that of IL-12 and IL-23 in activated RAW264.7 cells. Finally, in vivo subconjunctival injection of HC-HA/PTX3 significantly prolonged corneal allograft survival, suppressed macrophage infiltration, and promoted M2 polarization by upregulating Arg-1 and IL-10 but downregulating IL-12.

conclusionsHC-HA/PTX3 can suppress inflammatory responses in vivo by modulating both innate and adaptive immunity of macrophages and CD4(+) T cells.

Indexed as

Corneal TransplantationAcute-Phase ProteinsAdaptive ImmunityAllograftsAmnionAnimalsCD4-Positive T-LymphocytesCells, CulturedC-Reactive ProteinCytokinesDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryGraft RejectionHumansAcute-Phase ProteinsC-Reactive ProteinCytokinesHyaluronic AcidPentraxinsSerum Amyloid P-Componentamniotic membraneCD4+ T cellcorneal allograft rejectionmacrophage polarization

Identifiers

PMID24519420
PMCPMC4586971
OpenAlexW2087447278

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.