Evidence map›Paper›PMID 9261420›Full record

ArticleJournal of virology1997

CXCR4 expression during lymphopoiesis: implications for human immunodeficiency virus type 1 infection of the thymus.

S G Kitchen, J A Zack

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 115 citations in OpenAlex.

  1. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  2. Adaptive Immunodeficiency in WHIM Syndrome.International journal of molecular sciences · 2018
    Review
  3. Tracking migration during human T cell development.Cellular and molecular life sciences : CMLS · 2014
    Review
  4. Article
  5. Towards an HIV cure: a global scientific strategy.Nature reviews. Immunology · 2012
    Review
  6. Article
  7. Glut1-mediated glucose transport regulates HIV infection.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Glucose transporter 1 expression identifies a population of cycling CD4+ CD8+ human thymocytes with high CXCR4-induced chemotaxis.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  19. Article
  20. Article
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 1 institution in 1 country.

S G KitchenDepartment of Microbiology, Jonsson Comprehensive Cancer Center, Los Angeles, California, USA.
J A Zack
Comprehensive Blood & Cancer Center · US

Funding

IN VIVO PATHOGENESIS OF HIV1R37AI036059 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ZACK, JEROME A. · 1998 to 2007
$2.8M
IN VIVO PATHOGENESIS OF HIV-1R01AI036059 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ZACK, JEROME A. · 1994 to 1997
–
NIAID NIH HHS AI 36059
6 · The paper itself

Abstract

Human immunodeficiency virus type 1 (HIV-1) infection of the human thymus results in depletion of CD4-bearing thymocytes. This depletion is initially manifested in the immature CD4+/CD8+ thymocyte subset. To determine cellular factors involved in HIV infection in the thymus, we examined the expression of the recently identified viral coreceptor, CXCR4, on fresh human thymocytes and on human cells from SCID-hu (Thy/Liv) mice. CXCR4 is a member of the chemokine receptor family which is required along with CD4 for entry into the cell of syncytium-inducing (SI) HIV-1 strains. Our analyses show that CXCR4 expression is modulated during T-lymphoid differentiation such that immature thymocytes display an increased frequency and higher surface density of the coreceptor than do more mature cells. In addition, using an SI strain of HIV-1 which directs expression of a reporter protein on the surface of infected cells, we have found that the immature CD4+/CD8+ thymocytes that express the highest levels of both CD4 and CXCR4 are the cells that are preferentially infected and depleted by the virus in vitro. Thus, high levels of both primary receptor and coreceptor may allow efficient infection of the thymus by certain HIV-1 strains. This in part may explain the rapid disease progression seen in some HIV-infected children, where the thymus is actively involved in the production of new T lymphocytes.

Indexed as

AnimalsCells, CulturedDNA, ViralHematopoiesisHIV-1HumansLeukocytes, MononuclearMembrane ProteinsMiceMice, SCIDReceptors, CXCR4Receptors, HIVThymus GlandDNA, ViralMembrane ProteinsReceptors, CXCR4Receptors, HIV

Identifiers

PMID9261420
PMCPMC191976
OpenAlexW2141155285

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.