Evidence map›Paper›PMID 26098781›Full record

ArticlePloS one2015

Impact of Pre-Transplant Anti-T Cell Globulin (ATG) on Immune Recovery after Myeloablative Allogeneic Peripheral Blood Stem Cell Transplantation.

Sophie Servais, Catherine Menten-Dedoyart, Yves Beguin, Laurence Seidel, André Gothot, Coline Daulne, Evelyne Willems, Loïc Delens, Stéphanie Humblet-Baron, Muriel Hannon and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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  20. Long-Term Mixed Chimerism AfterFrontiers in oncology · 2021
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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

11 authors at 2 institutions in 1 country.

Sophie ServaisHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium; Bone Marrow Transplantation Unit, Department of Clinical Hematology, CHU of Liège, Liège, Belgium.
Catherine Menten-DedoyartHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium.
Yves BeguinHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium; Bone Marrow Transplantation Unit, Department of Clinical Hematology, CHU of Liège, Liège, Belgium.
Laurence SeidelDepartment of biostatistics, SIMÉ, CHU of Liège, Liège, Belgium.
André GothotDepartment of Laboratory Medicine, CHU of Liège, Liège, Belgium.
Coline DaulneHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium.
Evelyne WillemsBone Marrow Transplantation Unit, Department of Clinical Hematology, CHU of Liège, Liège, Belgium.
Loïc DelensHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium.
Stéphanie Humblet-BaronHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium.
Muriel HannonHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium.
Frédéric BaronHematology Research Unit, GIGA-I3, University of Liège, Liège, Belgium; Bone Marrow Transplantation Unit, Department of Clinical Hematology, CHU of Liège, Liège, Belgium.
University of Liège · BECentre Hospitalier Universitaire de Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPre-transplant infusion of rabbit anti-T cell globulin (ATG) is increasingly used as prevention of graft-versus-host disease (GVHD) after allogeneic peripheral blood stem cell transplantation (PBSCT). However, the precise impact of pre-transplant ATG on immune recovery after PBSCT is still poorly documented.

methodsIn the current study, we compared immune recovery after myeloablative PBSCT in 65 patients who either received (n = 37) or did not (n = 28) pre-transplant ATG-Fresenius (ATG-F). Detailed phenotypes of circulating T, B, natural killer (NK) and invariant NKT (iNKT) cells were analyzed by multicolor flow cytometry at serial time-points from day 40 to day 365 after transplantation. Thymic function was also assessed by sjTREC quantification. Serious infectious events were collected up to 2 years post-transplantation.

resultsPre-transplant ATG-F had a prolonged (for at least up to 1-year) and selective negative impact on the T-cell pool, while it did not impair the recovery of B, NK nor iNKT cells. Among T cells, ATG-F selectively compromised the recovery of naïve CD4+, central memory CD4+ and naïve CD8+ cells, while it spared effector memory T and regulatory T cells. Levels of sjTRECs were similar in both cohorts at 1-year after PBSCT, suggesting that ATG-F unlikely impaired thymopoiesis at long-term after PBSCT. Finally, the incidence and rate of serious infections were similar in both groups, while ATG-F patients had a lower incidence of grade II-IV acute graft-versus-host disease.

conclusionsPre-transplant ATG-F induces long-lasting modulation of the circulating T-cell pool after myeloablative PBSCT, that may participate in preventing graft-versus-host disease without deeply compromising anti-pathogen defenses.

Indexed as

AdolescentAdultB-LymphocytesCase-Control StudiesChildChild, PreschoolFemaleGlobulinsGraft vs Host DiseaseGranulocyte Precursor CellsHumansKiller Cells, NaturalMaleMiddle AgedPeripheral Blood Stem Cell TransplantationRetrospective StudiesGlobulins

Identifiers

PMID26098781
PMCPMC4476691
OpenAlexW2234725131

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.