Evidence map›Paper›PMID 26492933›Full record

ArticleBlood2015

Discordance in lymphoid tissue recovery following stem cell transplantation in rhesus macaques: an in vivo imaging study.

Robert E Donahue, Sharat Srinivasula, Naoya Uchida, Insook Kim, Alexis St Claire, Gorka Duralde, Paula DeGrange, Marisa St Claire, Richard C Reba, Aylin C Bonifacino and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Quantitative PET imaging of the CD4 pool in nonhuman primates.European journal of nuclear medicine and molecular imaging · 2022
    Article
  6. Article
  7. Article
  8. Deficits in the IgGClinical & translational immunology · 2020
    Article
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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

16 authors at 4 institutions in 1 country.

Robert E DonahueHematology Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD;
Sharat SrinivasulaBiostatistics Research Branch, Leidos Biomedical Research, Inc, Frederick National Laboratory for Cancer Research (FNLCR), Frederick, MD;
Naoya UchidaMolecular and Clinical Hematology Branch, NHLBI, NIH, Bethesda, MD;
Insook KimApplied/Developmental Research Directorate, Leidos Biomedical Research, Inc, FNLCR, Frederick, MD;
Alexis St ClaireDivision of Clinical Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD;
Gorka DuraldeDivision of Clinical Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD;
Paula DeGrangeIntegrated Research Facility, NIAID, NIH, Frederick, MD; and.
Marisa St ClaireIntegrated Research Facility, NIAID, NIH, Frederick, MD; and.
Richard C RebaCenter for Infectious Disease Imaging, Radiology and Imaging Sciences, Clinical Center.
Aylin C BonifacinoHematology Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD;
Allen E KrouseHematology Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD;
Mark E MetzgerHematology Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD;
Chang H PaikRadiopharmaceutical Laboratory, Nuclear Medicine, Radiology and Imaging Sciences, Clinical Center, and.
H Clifford LaneLaboratory of Immunoregulation, NIAID, NIH, Bethesda, MD.
John F TisdaleMolecular and Clinical Hematology Branch, NHLBI, NIH, Bethesda, MD;
Michele Di MascioDivision of Clinical Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD;
National Institute of Allergy and Infectious Diseases · USNational Heart Lung and Blood Institute · USNational Institutes of Health · USLeidos (United States) · US

Funding

NHLBI Animal Program DivisionZIGHL006020 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI CLARK, TANNIA · 2009 to 2025
$47.3M
Retroviral Mediated Gene Transfer Into Primate Hematopoietic CellsZICHL002338 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DONAHUE, ROBERT E · 2010 to 2018
$30.5M
CCR NIH HHS HHSN261200800001CIntramural NIH HHSNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Ionizing irradiation is used routinely to induce myeloablation and immunosuppression. However, it has not been possible to evaluate the extent of ablation without invasive biopsy. For lymphoid recovery, peripheral blood (PB) lymphocytes (PBLs) have been used for analysis, but they represent <2% of cells in lymphoid tissues (LTs). Using a combination of single-photon emission computed tomography imaging and a radiotracer ((99m)Tc-labeled rhesus immunoglobulin G1 anti-CD4R1 (Fab')2), we sequentially imaged CD4(+) cell recovery in rhesus macaques following total body irradiation (TBI) and reinfusion of vector-transduced, autologous CD34(+) cells. Our results present for the first time a sequential, real-time, noninvasive method to evaluate CD4(+) cell recovery. Importantly, despite myeloablation of circulating leukocytes following TBI, total depletion of CD4(+) lymphocytes in LTs such as the spleen is not achieved. The impact of TBI on LTs and PBLs is discordant, in which as few as 32.4% of CD4(+) cells were depleted from the spleen. In addition, despite full lymphocyte recovery in the spleen and PB, lymph nodes have suboptimal recovery. This highlights concerns about residual disease, endogenous contributions to recovery, and residual LT damage following ionizing irradiation. Such methodologies also have direct application to immunosuppressive therapy and other immunosuppressive disorders, such as those associated with viral monitoring.

Indexed as

Hematopoietic Stem Cell TransplantationTomography, Emission-Computed, Single-PhotonTransplantation ConditioningAnimalsBone MarrowCD4 AntigensCD4 Lymphocyte CountComputer SystemsGenes, ReporterGenes, SyntheticGenetic VectorsGreen Fluorescent ProteinsImmunoglobulin GLentivirusLymph NodesLymphoid TissueCD4 Antigensenhanced green fluorescent proteinGreen Fluorescent ProteinsImmunoglobulin G

Identifiers

PMID26492933
PMCPMC4671110
OpenAlexW2321631478

What OpenQuestion holds

Textmetadata
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.