Evidence map›Paper›PMID 20671122›Full record

ArticleBlood2010

Human NK cells of mice with reconstituted human immune system components require preactivation to acquire functional competence.

Till Strowig, Obinna Chijioke, Paolo Carrega, Frida Arrey, Sonja Meixlsperger, Patrick C Rämer, Guido Ferlazzo, Christian Münz

Abstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
–field-weighted citation impact
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

72 citing papers in PubMed.

  1. Article
  2. Review
  3. Nanomaterials Trigger Functional Anti-Tumoral Responses in Primary Human Immune Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. An engineered antibody-lectin conjugate targeting the HIV glycan shield protects humanized mice against HIV challenge.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  5. Article
  6. Fetal liver CD34Stem cell research & therapy · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Humanized MISTRG as a preclinicalFrontiers in immunology · 2023
    Article
  11. Article
  12. Article
  13. A Holistic Review of the Preclinical Landscape for Long-Acting Anti-infective Drugs Using HIV as a Paradigm.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Review
  14. Article
  15. Tofacitinib Suppresses Natural Killer CellsFrontiers in immunology · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

12 more citing papers are in PubMed but not listed here.

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

8 authors.

Till StrowigLaboratory of Viral Immunobiology, and Christopher H. Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, NY, USA.
Obinna Chijioke
Paolo Carrega
Frida Arrey
Sonja Meixlsperger
Patrick C Rämer
Guido Ferlazzo
Christian Münz

Funding

DC/NK interactions in human secondary lymphoid organsR01CA108609 · NCI · UNIVERSITY OF ZURICH · PI MUNZ, CHRISTIAN · 2004 to 2012
$1.8M
Endogenous MHC class II antigen processing via autophagyR01CA101741 · NCI · UNIVERSITY OF ZURICH · PI MUNZ, CHRISTIAN · 2006 to 2008
$883k
NCI NIH HHS R01 CA101741NCI NIH HHS R01CA101741NCI NIH HHS R01 CA108609NCI NIH HHS R01CA108609
6 · The paper itself

Abstract

To investigate human natural killer (NK)-cell reactivity in vivo we have reconstituted human immune system components by transplantation of human hematopoietic progenitor cells into NOD-scid IL2Rγ(null) mice. We demonstrate here that this model allows the development of all NK-cell subsets that are also found in human adult peripheral and cord blood, including NKp46(+)CD56(-) NK cells. Similar to human cord blood, NK cells from these reconstituted mice require preactivation by interleukin-15 to reach the functional competence of human adult NK cells. Mainly the terminally differentiated CD16(+) NK cells demonstrate lower reactivity without this stimulation. After preactivation, both CD16(+) and CD16(-) NK cells efficiently produce interferon-γ and degranulate in response to stimulation with NK cell-susceptible targets, including K562 erythroleukemia cells. NK-cell lines, established from reconstituted mice, demonstrate cytotoxicity against this tumor cell line. Importantly, preactivation can as well be achieved by bystander cell maturation via poly I:C stimulation in vitro and injection of this maturation stimulus in vivo. Preactivation in vivo enhances killing of human leukocyte antigen class I negative tumor cells after their adoptive transfer. These data suggest that a functional, but resting, NK-cell compartment can be established in immune-compromised mice after human hematopoietic progenitor cell transfer.

Indexed as

AdultAnimalsAntigens, CD34CD56 AntigenCell DegranulationCell DifferentiationCytotoxicity, ImmunologicFetal BloodGranzymesHematopoietic Stem CellsHumansImmune SystemImmunocompetenceInterferon-gammaInterleukin-15Killer Cells, NaturalAntigens, CD34CD56 AntigenGranzymesInterferon-gammaInterleukin-15Natural Cytotoxicity Triggering Receptor 1PerforinPoly I-CReceptors, Interleukin-2

Identifiers

PMID20671122
PMCPMC2993621

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.