Evidence map›Paper›PMID 26578348›Full record

ArticleBMC infectious diseases2015

Characterization of the inflammatory cell infiltrate and expression of costimulatory molecules in chronic echinococcus granulosus infection of the human liver.

A Vatankhah, J Halász, V Piurkó, T Barbai, E Rásó, J Tímár

Open access · goldAbstract read
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Article in BMC infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

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  11. Frontiers in cellular and infection microbiology · 2022
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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

6 authors at 1 institution in 1 country.

A Vatankhah2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. avatankhah@hotmail.com.
J Halász2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. halaszjudi@gmail.com.
V Piurkó2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. piurko.violetta@gmail.com.
T Barbai2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. tbarbai@gmail.com.
E Rásó2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. rasoerzs@gmail.com.
J Tímár2nd Department of Pathology, Semmelweis University, Üllői u. 93, 1091, Budapest, Hungary. jtimar@gmail.com.
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe local immune responses to chronic echinococcal infections in various organs are largely unknown. Since the liver is the most frequently involved organ in such infections in human we aimed to characterize the inflammatory as well as immune cell infiltrate around hydatid cysts in the liver and compared to common inflammatory processes of the liver.

methodSurgical samples from the liver of 21 cystic echinococcosis (CE) patients were studied and the distribution of different types of inflammatory and immune cells were determined by immunohistochemistry. Furthermore, expression levels of costimulatory CTLA4, CD28, CD80 and CD86 molecules were measured at RNA level by PCR. Liver biopsy samples from patients with steatohepatitis (SH, n = 11) and chronic hepatitis (CH, n = 11) were used as non-inflammatory and chronic inflammatory controls, respectively. The composition and density of the inflammatory and immune cell infiltrates have been compared by using morphometry.

resultsCD3+ T cells predominated the inflammatory infiltrate in all pathological processes, while in CE samples CD20+ B cells, in CH samples CD68+ macrophages were also frequent. Both myeloperoxidase (MPO) + leukocytes and CD68+ macrophages were found to be significantly decreased in CE as compared to either SH or CH samples. Concerning T cell subtypes, only CD8+ T cells were found to be significantly decreased in SH samples. CD1a + dendritic cells were almost completely missing from CE biopsies unlike in any other sample types. There were no differences detected in the mRNA expression of costimulatory molecules except decreased expression of CD28 in CE samples.

conclusionIn the hydatid lesions of the liver of chronic echinococcal infections T cell-mediated immunity seems to be impaired as compared to other types of chronic inflammatory processes, suggesting an immunosuppressive role for Echinococcus granulosus, which deserve further attentions.

Indexed as

AdolescentAdultAgedAnimalsAntigens, CDB7-2 AntigenChildChild, PreschoolCTLA-4 AntigenDendritic CellsEchinococcosis, HepaticEchinococcus granulosusFemaleHumansImmunity, CellularImmunohistochemistryAntigens, CDB7-2 AntigenCTLA-4 Antigen

Identifiers

PMID26578348
PMCPMC4647452
OpenAlexW2177363221

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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.