Evidence map›Paper›PMID 14632753›Full record

ArticleClinical and experimental immunology2003

Loss of the CD56hiCD16- NK cell subset and NK cell interferon-gamma production during antiretroviral therapy for HIV-1: partial recovery by human growth hormone.

M R Goodier, N Imami, G Moyle, B Gazzard, F Gotch

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

M R GoodierDepartment of Immunology, Imperial College London, Faculty of Medicine, Chelsea and Westminster Hospital, London, UK. m.goodier@ic.ac.uk
N Imami
G Moyle
B Gazzard
F Gotch
Imperial College London · GBChelsea and Westminster Hospital · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Previous studies have shown that human natural killer (NK) cells are lost from the periphery and are functionally suppressed during HIV-1 infection, and that the administration of highly active antiretroviral therapy (HAART) results in a recovery of NK cell numbers in HIV-1-infected individuals. However, despite this recovery, interleukin (IL)-2 + IL-12-driven interferon (IFN)-gamma production by NK cells has been shown to remain suppressed after HAART. Here we show that the innate immune factor IL-15 in combination with IL-12 is also unable to recover NK cell IFN-gamma production in HAART-treated individuals. Furthermore, we also demonstrate an imbalance in the distribution of CD56loCD16hi and CD56hiCD16- NK subsets after successful HAART, CD56hiCD16- cells being reduced substantially in HIV-1 patients on HAART. Treatment of patients with combined human growth hormone and antiretroviral therapy resulted in further enhancement in the absolute numbers and the proportion of NK cells in some individuals in the absence of parallel effects on CD4+ T cells. Furthermore, in these individuals HAART with growth hormone resulted in an enhancement of cytokine-driven NK cell activation and IFN-gamma production compared to the HAART-only baseline.

Indexed as

HIV-1Antigens, CDAntigens, Differentiation, T-LymphocyteAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD56 AntigenCD69 AntigensCells, CulturedDrug Therapy, CombinationFlow CytometryHIV InfectionsHuman Growth HormoneHumansInterferon-gammaInterleukin-12Interleukin-15Antigens, CDAntigens, Differentiation, T-LymphocyteAnti-HIV AgentsCD56 AntigenCD69 AntigensHuman Growth HormoneInterferon-gammaInterleukin-12Interleukin-15Lectins, C-TypeReceptors, IgG

Identifiers

PMID14632753
PMCPMC1808890
OpenAlexW2045525130

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.