Evidence map›Paper›PMID 18790456›Full record

ReviewBest practice & research. Clinical haematology2008

Immune reconstitution and implications for immunotherapy following haematopoietic stem cell transplantation.

Kirsten M Williams, Ronald E Gress

Abstract readReview
In one paragraph

Review in Best practice & research. Clinical haematology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

53 citing papers in PubMed, 114 citations in OpenAlex.

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  19. Pathogen-Specific T Cells Beyond CMV, EBV and Adenovirus.Current hematologic malignancy reports · 2019
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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

2 authors at 2 institutions in 1 country.

Kirsten M WilliamsExperimental Transplantation and Immunology Branch, National Cancer Institute, NIH, CRC-3E-3300, 10 Center Drive, Bethesda, MD 20892, USA.
Ronald E Gress
National Cancer Institute · USNational Institutes of Health · US

Funding

Immune ReconstitutionZIABC010525 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2023
$21.9M
Transplant ModelsZIABC010957 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2016
$10.1M
Immune ReconstitutionZ01BC010525 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD E. · 2003 to 2008
$4.9M
Intramural NIH HHS Z01 BC010525Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Recovery of a fully functional immune system is a slow and often incomplete process following allogeneic stem cell transplantation. While innate immunity reconstitutes quickly, adaptive B- and especially T-cell lymphopoeisis may be compromised for years following transplantation. In large part, these immune system deficits are due to the decrease, or even absence, of thymopoiesis following transplantation. Thereby, T-cell reconstitution initially relies upon expansion of mature donor T cells; a proliferation driven by high cytokine levels and the presence of allo-reactive antigens. This peripheral mechanism of T-cell generation may have important clinical consequences. By expanding tumouricidal T cells, it may provide a venue to enhance T-cellular immunotherapy following transplantation. Alternatively, decreased thymic function may impair long-term anti-tumour immunity and increase the likelihood of graft-versus-host disease.

Indexed as

Hematopoietic Stem Cell TransplantationB-LymphocytesBone Marrow TransplantationDendritic CellsGraft vs Host DiseaseHumansImmunity, InnateImmunotherapyKiller Cells, NaturalLeukemiaNeoplasmsNeutrophilsT-LymphocytesTransplantation Conditioning

Identifiers

PMID18790456
PMCPMC2577193
OpenAlexW2046100979

What OpenQuestion holds

Textmetadata
LicenceTDM
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.