Evidence map›Paper›PMID 35894710›Full record

ArticleImmunity, inflammation and disease2022

Peripheral blood and bronchoalveolar leukocyte profile in lung transplant recipients and their changes according to immunosuppressive regimen: A single-center experience.

Zsuzsanna Jáky-Kováts, Melinda Vámos, Zsolt István Komlósi, András Bikov, Ildikó Madurka, Gergő Szűcs, Veronika Müller, Anikó Bohács

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In one paragraph

Article in Immunity, inflammation and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 2 countries.

Zsuzsanna Jáky-KovátsDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-6145-6595
Melinda VámosDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Zsolt István KomlósiDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
András BikovDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Ildikó MadurkaDepartment of Thoracic Surgery, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Gergő SzűcsDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-3446-0406
Veronika MüllerDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Anikó BohácsDepartment of Pulmonology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfter lung transplantation (LuTX), lower respiratory tract infections (LRTI) and acute cellular rejection (ACR) are associated with changes in peripheral blood and bronchoalveolar lavage fluid mononuclear cell profile (PBMC and BALIC). PBMC is also influenced by immunosuppressive regimen and its changes with postoperative time. First-year PBMC and BALIC changes were evaluated in this study with rabbit anti-thymocyte globulin (ATG) and alemtuzumab (AL) induction therapy.

methodsIn total, 64 LuTX recipients were included, 53 of them received AL and 11 ATG as induction therapy. PBMC and BALIC were examined routinely and in cases suspicious of infection and/or rejection. A PBMC- and BALIC-based algorithm for infection and rejection prediction was also tested.

resultsIn the AL group, peripheral blood lymphocyte and basophil cell numbers were significantly reduced, while the neutrophil cell number elevation during LRTI was significantly higher compared to the control. Early postoperative measurements showed a lower BALIC lymphocyte count. The algorithm had 17% sensitivity and 94% specificity for ACR in all patients and 33% sensitivity and 95% specificity for ACR with coexisting LRTI.

conclusionBALIC is not significantly influenced by the immunosuppressive regimen. PBMC- and BALIC-based algorithm may improve the differential diagnosis of ACR.

Indexed as

Leukocytes, MononuclearTransplant RecipientsAlemtuzumabGraft RejectionHumansImmunosuppressive AgentsLungAlemtuzumabImmunosuppressive Agentsacute cellular rejectionbronchoalveolar lavagedifferential diagnosislung transplantPBMC

Identifiers

PMID35894710
PMCPMC9274796
OpenAlexW4285020520

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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.