Evidence map›Paper›PMID 25367120›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Immature recent thymic emigrants are eliminated by complement.

Fan-Chi Hsu, Michael J Shapiro, Meibo W Chen, Douglas C McWilliams, Lauren M Seaburg, Sarah N Tangen, Virginia Smith Shapiro

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Polysialic Acid in the Immune System.Frontiers in immunology · 2021
    Review
  8. TCR-α/β CD4Journal of leukocyte biology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Histone deacetylase function in CD4Nature reviews. Immunology · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Histone Deacetylase 3 Is Required for T Cell Maturation.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  20. T Cell Adolescence: Maturation Events Beyond Positive Selection.Journal of immunology (Baltimore, Md. : 1950) · 2015
    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

7 authors at 1 institution in 1 country.

Fan-Chi HsuDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Michael J ShapiroDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Meibo W ChenDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Douglas C McWilliamsDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Lauren M SeaburgDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Sarah N TangenDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Virginia Smith ShapiroDepartment of Immunology, Mayo Clinic, Rochester, MN 55905 shapiro.virginia1@mayo.edu.
Mayo Clinic in Arizona · US

Funding

Regulation of T cell maturationR01AI083279 · NIAID · MAYO CLINIC ROCHESTER · PI SHAPIRO, VIRGINIA SMITH · 2010 to 2019
$3.8M
NIAID NIH HHS R01 AI083279
6 · The paper itself

Abstract

Recent thymic emigrants (RTEs) must undergo phenotypic and functional maturation to become long-lived mature naive T cells. In CD4-cre NKAP conditional knockout mice, NKAP-deficient RTEs fail to complete T cell maturation. In this study, we demonstrate that NKAP-deficient immature RTEs do not undergo apoptosis, but are eliminated by complement. C3, C4, and C1q are bound to NKAP-deficient peripheral T cells, demonstrating activation of the classical arm of the complement pathway. As thymocytes mature and exit to the periphery, they increase sialic acid incorporation into cell surface glycans. This is essential to peripheral lymphocyte survival, as stripping sialic acid with neuraminidase leads to the binding of natural IgM and complement fixation. NKAP-deficient T cells have a defect in sialylation on cell surface glycans, leading to IgM recruitment. We demonstrate that the defect in sialylation is due to aberrant α2,8-linked sialylation, and the expression of three genes (ST8sia1, ST8sia4, and ST8sia6) that mediate α2,8 sialylation are downregulated in NKAP-defcient RTEs. The maturation of peripheral NKAP-deficient T cells is partially rescued in a C3-deficient environment. Thus, sialylation during T cell maturation is critical to protect immature RTEs from complement in the periphery.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, B-LymphocyteApoptosisCD55 AntigensCell DifferentiationCell MovementCell SurvivalComplement ActivationComplement C3Complement System ProteinsGene ExpressionImmunoglobulin MImmunophenotypingLeukocyte Common AntigensMiceAntigens, CDAntigens, Differentiation, B-LymphocyteCD55 AntigensComplement C3Complement System ProteinsImmunoglobulin MLeukocyte Common AntigensN-Acetylneuraminic AcidNKAP protein, mouseRepressor ProteinsSiglece protein, mouse

Identifiers

PMID25367120
PMCPMC4332405
OpenAlexW1748089851

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.