Evidence map›Paper›PMID 10811848›Full record

ArticleThe Journal of clinical investigation2000

HIV-specific cytotoxic T lymphocytes traffic to lymph nodes and localize at sites of HIV replication and cell death.

S J Brodie, B K Patterson, D A Lewinsohn, K Diem, D Spach, P D Greenberg, S R Riddell, L Corey

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.7field-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

27 citing papers in PubMed, 91 citations in OpenAlex.

  1. Incomplete reconstitution of T cell subsets on combination antiretroviral therapy in the AIDS Clinical Trials Group protocol 384.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2009
    Trial
  2. Article
  3. Article
  4. Enhanced anti-HIV efficacy of indinavir after inclusion in CD4-targeted lipid nanoparticles.Journal of acquired immune deficiency syndromes (1999) · 2012
    Article
  5. Article
  6. Article
  7. Review
  8. Dynamic regulation of functionally distinct virus-specific T cells.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  9. Article
  10. NanoART, neuroAIDS and CNS drug delivery.Nanomedicine (London, England) · 2009
    Review
  11. Article
  12. Article
  13. Article
  14. Genetic therapies against HIV.Nature biotechnology · 2007
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

S J BrodieDepartment of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA. sjbrodie@u.washington.edu
B K Patterson
D A Lewinsohn
K Diem
D Spach
P D Greenberg
S R Riddell
L Corey
University of Washington · USNorthwestern University · US

Funding

THE PERINATAL COMPLICATIONS OF ASYMPTOMATIC GENITAL HERPES SIMPLEX VIRUSP01AI030731 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 1991 to 2017
$34.3M
IMMUNOLOGY AND MOLECULAR VIROLOGY OF ACUTE HIV INFECTIONU01AI041535 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI COREY, LAWRENCE · 1997 to 2003
$6.0M
TRANSFER OF CD4+ T CELL CLONES WITH GENES INHIBITING HIVU19AI036613 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CARTER, BARRIE J · 1994 to 1997
–
NIAID NIH HHS AI-30731NIAID NIH HHS AI-36613NIAID NIH HHS AI-41535NIAID NIH HHS P01 AI030731
6 · The paper itself

Abstract

We have tracked the in vivo migration and have identified in vivo correlates of cytotoxic T-lymphocyte (CTL) activity in HIV-seropositive subjects infused with autologous gene-marked CD8(+) HIV-specific CTL. The number of circulating gene-marked CTL ranged from 1.6 to 3.5% shortly after infusion to less than 0.5% 2 weeks later. Gene-marked CTL were present in the lymph node at 4.5- to 11-fold excess and colocalized within parafollicular regions of the lymph node adjacent to cells expressing HIV tat fusion transcripts, a correlate of virus replication. The CTL clones expressed the CCR5 receptor and localized among HIV-infected cells expressing the ligands MIP-1alpha and MIP-1beta, CC-chemokines produced at sites of virus replication. Aggregates of apoptotic cells and cells expressing granzyme-B localized within these same sites. In contrast, lymph node sections from untreated HIV-seropositive subjects, all with significant viral burden (> 50,000 HIV RNA copies/mL plasma), showed no CC-chemokine expression and exhibited only sporadic and randomly distributed cells expressing granzymes and/or apoptotic cells. These studies show that the infused CTL specifically migrate to sites of HIV replication and retain their antigen-specific cytolytic potential. Moreover, these studies provide a methodology that will facilitate studies of both the magnitude and functional phenotype of Ag-specific CD8(+) T cells in vivo.

Indexed as

Adoptive TransferBase SequenceCell DeathCell MovementDNA PrimersGene Transfer TechniquesHIVHIV SeropositivityHumansIn Situ HybridizationLymph NodesPolymerase Chain ReactionT-Lymphocytes, CytotoxicVirus ReplicationDNA Primers

Identifiers

PMID10811848
PMCPMC315465
OpenAlexW2124115029

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.