Evidence map›Paper›PMID 11470920›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Perforin-low memory CD8+ cells are the predominant T cells in normal humans that synthesize the beta -chemokine macrophage inflammatory protein-1beta.

R Kamin-Lewis, S F Abdelwahab, C Trang, A Baker, A L DeVico, R C Gallo, G K Lewis

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. CD4Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. HIV-induced changes in T cell signaling pathways.Journal of immunology (Baltimore, Md. : 1950) · 2008
    Article
  9. Article
  10. Article
  11. 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

7 authors at 2 institutions in 1 country.

R Kamin-LewisDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA. kaminlew@umbi.umd.edu
S F Abdelwahab
C Trang
A Baker
A L DeVico
R C Gallo
G K Lewis
University of Maryland, Baltimore · USBiotechnology Institute · US

Funding

VACCINE SAFETY AND IMMUNOGENICITYP01AI047490 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI LEWIS, GEORGE K · 2000 to 2005
$5.7M
MACROPHAGE DERIVED CHEMOKINE AND HIV INFECTIONR01HL063647 · NHLBI · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI DEVICO, ANTHONY L · 1999 to 2003
$1.2M
HIV-1 PASSIVE IMMUNITY AGAINST CORECEPTOR INTERACTIONSR01HL059796 · NHLBI · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI DEVICO, ANTHONY L · 1997 to 2001
$673k
SINGLE CHAIN HIV GP120-CD4 COMPLEXR21AI047066 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI DEVICO, ANTHONY L · 2000 to 2001
$446k
PROTECTIVE IMMUNITY AGAINST HIV ENVELOPE/RECEPTOR COMPLEXESP01AI043046 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI LEWIS, GEORGE K · 1998 to 1998
–
CD8+ T CELLS IN PRIMARY INFECTIONR21AI044736 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAMIN-LEWIS, ROBERTA · 1998 to 1999
–
NHLBI NIH HHS HL59796NHLBI NIH HHS HL63647NIAID NIH HHS AI3892NIAID NIH HHS AI43046NIAID NIH HHS AI44736NIAID NIH HHS AI47066NIAID NIH HHS AI47490NIAID NIH HHS P01 AI047490
6 · The paper itself

Abstract

The synthesis of antiviral beta-chemokines has joined cytolysis as a potential mechanism for the control of HIV-1 infection by CD8(+) T cells. Recent evidence suggests that these two effector functions can diverge in some individuals infected with HIV-1; however, little is known about the CD8(+) T cell subsets in normal individuals that synthesize antiviral beta-chemokines. In this report, we have used mutliparameter flow cytometry to characterize the T cell subsets that secrete the antiviral beta-chemokine macrophage inflammatory protein (MIP)-1beta. These studies have shown: (i) CD8(+) cells are the predominant T cell subset that synthesizes MIP-1beta; (ii) MIP-1beta and IFN-gamma are synthesized congruently in most CD8(+) T cells; however, significant numbers of these cells synthesize only one of these effector molecules; (iii) approximately 60% of the CD8(+) T cells that synthesize MIP-1beta lack perforin; (iv) MIP-1beta is synthesized with approximately equal frequency by CD28(+) and CD28(-) subpopulations of CD8(+) T cells; (v) MIP-1beta is synthesized by three distinct CD8(+) T cell subsets defined by the expression of CD45R0 and CD62L; and (vi) MIP-1beta is not synthesized in short-term cultures of naive CD8(+) T cells. These results demonstrate substantial subset heterogeneity of MIP-1beta synthesis among CD8(+) T cells and suggest that these subsets should be evaluated as correlates of protective immunity against HIV-1.

Indexed as

Immunologic MemoryCD28 AntigensCD8-Positive T-LymphocytesChemokine CCL4Flow CytometryHumansInterferon-gammaLymphocyte ActivationMacrophage Inflammatory ProteinsMembrane GlycoproteinsPerforinPore Forming Cytotoxic ProteinsCD28 AntigensChemokine CCL4Interferon-gammaMacrophage Inflammatory ProteinsMembrane GlycoproteinsPerforinPore Forming Cytotoxic Proteins

Identifiers

PMID11470920
PMCPMC55412
OpenAlexW1970568343

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.