Evidence map›Paper›PMID 32722785›Full record

ArticleBlood advances2020

Rapidly expanded partially HLA DRB1-matched fungus-specific T cells mediate in vitro and in vivo antifungal activity.

Gloria Castellano-González, Helen M McGuire, Fabio Luciani, Leighton E Clancy, Ziduo Li, Selmir Avdic, Brendan Hughes, Mandeep Singh, Barbara Fazekas de St Groth, Giorgia Renga and 4 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 14 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

14 authors at 4 institutions in 2 countries.

Gloria Castellano-GonzálezWestmead Institute for Medical Research, Sydney, NSW, Australia.
Helen M McGuireCharles Perkins Centre and.
Fabio LucianiKirby Institute, University of New South Wales, Sydney, NSW, Australia.
Leighton E ClancyWestmead Institute for Medical Research, Sydney, NSW, Australia.
Ziduo LiWestmead Institute for Medical Research, Sydney, NSW, Australia.
Selmir AvdicWestmead Institute for Medical Research, Sydney, NSW, Australia.
Brendan HughesKirby Institute, University of New South Wales, Sydney, NSW, Australia.
Mandeep SinghKirby Institute, University of New South Wales, Sydney, NSW, Australia.
Barbara Fazekas de St GrothCharles Perkins Centre and.
Giorgia RengaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Marilena ParianoDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Marina M BelletDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Luigina RomaniDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
David J GottliebWestmead Institute for Medical Research, Sydney, NSW, Australia.
University of Perugia · ITWestmead Institute for Medical Research · AUThe University of Sydney · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invasive fungal infections are a major cause of disease and death in immunocompromised hosts, including patients undergoing allogeneic hematopoietic stem cell transplant (HSCT). Recovery of adaptive immunity after HSCT correlates strongly with recovery from fungal infection. Using initial selection of lymphocytes expressing the activation marker CD137 after fungal stimulation, we rapidly expanded a population of mainly CD4+ T cells with potent antifungal characteristics, including production of tumor necrosis factor α, interferon γ, interleukin-17, and granulocyte-macrophage colony stimulating factor. Cells were manufactured using a fully good manufacturing practice-compliant process. In vitro, the T cells responded to fungal antigens presented on fully and partially HLA-DRB1 antigen-matched presenting cells, including when the single common DRB1 antigen was allelically mismatched. Administration of antifungal T cells lead to reduction in the severity of pulmonary and cerebral infection in an experimental mouse model of Aspergillus. These data support the establishment of a bank of cryopreserved fungus-specific T cells using normal donors with common HLA DRB1 molecules and testing of partially HLA-matched third-party donor fungus-specific T cells as a potential therapeutic in patients with invasive fungal infection after HSCT.

Indexed as

Antifungal AgentsHematopoietic Stem Cell TransplantationAnimalsAntigen-Presenting CellsFungiHLA-DRB1 ChainsHumansMiceAntifungal AgentsHLA-DRB1 Chains

Identifiers

PMID32722785
PMCPMC7391149
OpenAlexW3045792615

What OpenQuestion holds

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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.