Evidence map›Paper›PMID 25071784›Full record

ArticleFrontiers in immunology2014

Communication between Human Dendritic Cell Subsets in Tuberculosis: Requirements for Naive CD4(+) T Cell Stimulation.

Laura Lozza, Maura Farinacci, Marina Bechtle, Manuela Stäber, Ulrike Zedler, Andrea Baiocchini, Franca Del Nonno, Stefan H E Kaufmann

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 14% 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, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Pathological and protective roles of dendritic cells inFrontiers in cellular and infection microbiology · 2022
    Review
  5. Article
  6. Article
  7. Dendritic Cell-Based Cancer Vaccines.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Striking the right immunological balance prevents progression of tuberculosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Human dendritic cell subsets and function in health and disease.Cellular and molecular life sciences : CMLS · 2015
    Review
  17. Observational
  18. Article
  19. 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

8 authors at 3 institutions in 2 countries.

Laura LozzaDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Maura FarinacciDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Marina BechtleDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Manuela StäberDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Ulrike ZedlerDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Andrea BaiocchiniPathology Division, National Institute for Infectious Disease 'Lazzaro Spallanzani' , Rome , Italy.
Franca Del NonnoPathology Division, National Institute for Infectious Disease 'Lazzaro Spallanzani' , Rome , Italy.
Stefan H E KaufmannDepartment of Immunology, Max Planck Institute for Infection Biology , Berlin , Germany.
Max Planck Institute for Infection Biology · DEIstituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITMax Planck Society · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human primary dendritic cells (DCs) are heterogeneous by phenotype, function, and tissue localization and distinct from inflammatory monocyte-derived DCs. Current information regarding the susceptibility and functional role of primary human DC subsets to Mycobacterium tuberculosis (Mtb) infection is limited. Here, we dissect the response of different primary DC subsets to Mtb infection. Myeloid CD11c(+) cells and pDCs (C-type lectin 4C(+) cells) were located in human lymph nodes (LNs) of tuberculosis (TB) patients by histochemistry. Rare CD141(hi) DCs (C-type lectin 9A(+) cells) were also identified. Infection with live Mtb revealed a higher responsiveness of myeloid CD1c(+) DCs compared to CD141(hi) DCs and pDCs. CD1c(+) DCs produced interleukin (IL)-6, tumor necrosis factor α, and IL-1β but not IL-12p70, a cytokine important for Th1 activation and host defenses against Mtb. Yet, CD1c(+) DCs were able to activate autologous naïve CD4(+) T cells. By combining cell purification with fluorescence-activated cell sorting and gene expression profiling on rare cell populations, we detected in responding CD4(+) T cells, genes related to effector-cytolytic functions and transcription factors associated with Th1, Th17, and Treg polarization, suggesting multifunctional properties in our experimental conditions. Finally, immunohistologic analyses revealed contact between CD11c(+) cells and pDCs in LNs of TB patients and in vitro data suggest that cooperation between Mtb-infected CD1c(+) DCs and pDCs favors stimulation of CD4(+) T cells.

Indexed as

CD141hi DCsCD1c+ DCsCD4+ T cellshumanMycobacterium tuberculosisplasmacytoid DCs

Identifiers

PMID25071784
PMCPMC4094910
OpenAlexW2035262561

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.