Evidence map›Paper›PMID 18573906›Full record

Trial reportThe Journal of experimental medicine2008

Administration of rhIL-7 in humans increases in vivo TCR repertoire diversity by preferential expansion of naive T cell subsets.

Claude Sportès, Frances T Hakim, Sarfraz A Memon, Hua Zhang, Kevin S Chua, Margaret R Brown, Thomas A Fleisher, Michael C Krumlauf, Rebecca R Babb, Catherine K Chow and 10 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of experimental medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01368107 (A Randomised, Multicentric, Phase 2a Study Evaluating the Impact of an Immunotherapy by IL-7 on CD4 Lymphopenia, Risks of Severe Haematological Toxicity and Tumor Progression in Metastatic Breast Cancer Patients), which is not on this map. Cited by 281 papers.

0numbers the graph read from it
0cells of the map it votes in
281citing papers in PubMed
17.8field-weighted citation impact, top 1% 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.

NCT01368107 phase2completednot on this mapstarted 2011, after this paper: background citation

A Randomised, Multicentric, Phase 2a Study Evaluating the Impact of an Immunotherapy by IL-7 on CD4 Lymphopenia, Risks of Severe Haematological Toxicity and Tumor Progression in Metastatic Breast Cancer Patients

TypeinterventionalSponsorCentre Leon BerardRan2011 to 2014Enrolled24ConditionsMetastatic Breast CancerArmsplacebo, interleukin 7
3 · Its place in the literature

Who cites it

281 citing papers in PubMed, 463 citations in OpenAlex.

  1. Trial
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  5. Adjuvant Immunotherapy to Improve Outcome in High-Risk Pediatric Sarcomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Trial
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  10. Trial
  11. Article
  12. Review
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  15. CD8Science China. Life sciences · 2026
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Machine learning in AIRR diagnostics: Advances and applications.Immunoinformatics (Amsterdam, Netherlands) · 2025
    Article

221 more citing papers are in PubMed but not listed here.

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

20 authors at 6 institutions in 3 countries.

Claude SportèsExperimental Transplantation and Immunology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA. csportes@mail.nih.gov
Frances T Hakim
Sarfraz A Memon
Hua Zhang
Kevin S Chua
Margaret R Brown
Thomas A Fleisher
Michael C Krumlauf
Rebecca R Babb
Catherine K Chow
Terry J Fry
Julie Engels
Renaud Buffet
Michel Morre
Robert J Amato
David J Venzon
Robert Korngold
Andrew Pecora
Ronald E Gress
Crystal L Mackall
Cancer Institute (WIA) · INCenter for Cancer Research · USHackensack University Medical Center · USNational Institutes of Health Clinical Center · USResearch Institute of Radiology · BYTexas Medical Center · US

Funding

Immune reconstitution following autologous and allogeneic stem cell transplantZICBC010934 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FLOMERFELT, FRANCIS · 2009 to 2022
$10.0M
Biology of T Cell DepletionZIABC011069 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MACKALL, CRYSTAL · 2009 to 2015
$4.7M
ETIOLOGY &PATHOGENESIS OF MURINE GRAFT-VS-HOST DISEASER01HL055593 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI KORNGOLD, ROBERT · 1995 to 2009
$3.4M
BIOSTATISTICS AND DATA MANAGEMENT SECTIONZ01SC007202 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI STEINBERG, SETH M · 1996 to 2008
$1.5M
Clinical TrialsZ01BC010960 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2008 to 2008
$707k
Developing Immune Based TherapiesZ01BC011072 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MACKALL, CRYSTAL · 2008 to 2008
$686k
NHLBI NIH HHS R01 HL055593PHS HHS #01649
6 · The paper itself

Abstract

Interleukin-7 (IL-7) is a homeostatic cytokine for resting T cells with increasing serum and tissue levels during T cell depletion. In preclinical studies, IL-7 therapy exerts marked stimulating effects on T cell immune reconstitution in mice and primates. First-in-human clinical studies of recombinant human IL-7 (rhIL-7) provided the opportunity to investigate the effects of IL-7 therapy on lymphocytes in vivo. rhIL-7 induced in vivo T cell cycling, bcl-2 up-regulation, and a sustained increase in peripheral blood CD4(+) and CD8(+) T cells. This T cell expansion caused a significant broadening of circulating T cell receptor (TCR) repertoire diversity independent of the subjects' age as naive T cells, including recent thymic emigrants (RTEs), expanded preferentially, whereas the proportions of regulatory T (T reg) cells and senescent CD8(+) effectors diminished. The resulting composition of the circulating T cell pool more closely resembled that seen earlier in life. This profile, distinctive among cytokines under clinical development, suggests that rhIL-7 therapy could enhance and broaden immune responses, particularly in individuals with limited naive T cells and diminished TCR repertoire diversity, as occurs after physiological (age), pathological (human immunodeficiency virus), or iatrogenic (chemotherapy) lymphocyte depletion.

Indexed as

Age FactorsAnimalsCD4 Lymphocyte CountCD8-Positive T-LymphocytesFemaleHIVHIV InfectionsHumansInterleukin-7Lymphocyte DepletionMaleMiceNeoplasmsProto-Oncogene Proteins c-bcl-2Receptors, Antigen, T-CellRecombinant ProteinsIL7 protein, humanInterleukin-7Proto-Oncogene Proteins c-bcl-2Receptors, Antigen, T-CellRecombinant Proteins

Identifiers

PMID18573906
PMCPMC2442646
OpenAlexW2105011122

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.