Evidence map›Paper›PMID 21993602›Full record

ArticleMucosal immunology2012

Altered distribution of mucosal NK cells during HIV infection.

M Sips, G Sciaranghella, T Diefenbach, A-S Dugast, C T Berger, Q Liu, D Kwon, M Ghebremichael, J D Estes, M Carrington and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Intestinal Microbiota Dysbiosis Promotes Mucosal Barrier Damage and Immune Injury in HIV-Infected Patients.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2023
    Review
  4. Review
  5. Article
  6. Preterm Birth in Women With HIV: The Role of the Placenta.Frontiers in global women's health · 2022
    Review
  7. Article
  8. Gut Innate Immunity and HIV Pathogenesis.Current HIV/AIDS reports · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Differential Effect of Mucosal NKp44Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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

14 authors at 3 institutions in 1 country.

M SipsRagon Institute of Massachusetts General Hospital, Harvard University and Massachusetts Institute of Technology, Boston, Massachusetts, USA.
G Sciaranghella
T Diefenbach
A-S Dugast
C T Berger
Q Liu
D Kwon
M Ghebremichael
J D Estes
M Carrington
J N Martin
S G Deeks
P W Hunt
G Alter
Ragon Institute of MGH, MIT and Harvard · USUniversity of California, San Francisco · USFrederick National Laboratory for Cancer Research · US

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALLORY O JOHNSON · 1988 to 2026
$93.6M
Effects of genetic polymorphism in MHC, KIR, and related loci on human diseaseZIABC010791 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CARRINGTON, MARY N. · 2009 to 2025
$18.2M
Demystifying the antiviral activity of the IgG3+ antibody responseR01AI080289 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI JUELG, BORIS DOMINIK · 2009 to 2024
$4.1M
Gut mucosal immunity to HIV-1 in controlled and progressive infectionK08AI084546 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI KWON, DOUGLAS · 2009 to 2012
$498k
NCI NIH HHS HHSN261200800001ENIAID NIH HHS K08 AI084546NIAID NIH HHS P30 AI027763NIAID NIH HHS R01 AI080289
6 · The paper itself

Abstract

The human gut mucosa is a major site of human immunodeficiency virus (HIV) infection and infection-associated pathogenesis. Increasing evidence shows that natural killer (NK) cells have an important role in control of HIV infection, but the mechanism(s) by which they mediate antiviral activity in the gut is unclear. Here, we show that two distinct subsets of NK cells exist in the gut, one localized to intraepithelial spaces (intraepithelial lymphocytes, IELs) and the other to the lamina propria (LP). The frequency of both subsets of NK cells was reduced in chronic infection, whereas IEL NK cells remained stable in spontaneous controllers with protective killer immunoglobulin-like receptor/human leukocyte antigen genotypes. Both IEL and LP NK cells were significantly expanded in immunological non-responsive patients, who incompletely recovered CD4+ T cells on highly active antiretroviral therapy (HAART). These data suggest that both IEL and LP NK cells may expand in the gut in an effort to compensate for compromised CD4+ T-cell recovery, but that only IEL NK cells may be involved in providing durable control of HIV in the gut.

Indexed as

Antiretroviral Therapy, Highly ActiveBiomarkers, PharmacologicalBiopsyCell MovementDNA Mutational AnalysisGenotypeHIVHIV InfectionsHLA AntigensHumansIntestinal MucosaKiller Cells, NaturalLymphocyte SubsetsPolymorphism, GeneticReceptors, KIRBiomarkers, PharmacologicalHLA AntigensReceptors, KIR

Identifiers

PMID21993602
PMCPMC3740353
OpenAlexW2107031485

What OpenQuestion holds

Textmetadata
LicenceTDM
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.