Evidence map›Paper›PMID 24659689›Full record

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

Mycobacterium tuberculosis impairs dendritic cell functions through the serine hydrolase Hip1.

Ranjna Madan-Lala, Jonathan Kevin Sia, Rebecca King, Toidi Adekambi, Leticia Monin, Shabaana A Khader, Bali Pulendran, Jyothi Rengarajan

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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-weighted citation impact, top 11% 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, 70 citations in OpenAlex.

  1. HowVaccines · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Molecular Genomic Analyses ofMicroorganisms · 2024
    Article
  7. Roles of Lipolytic enzymes inFrontiers in microbiology · 2024
    Review
  8. Review
  9. Review
  10. Early innate cell interactions withFrontiers in immunology · 2023
    Review
  11. Tuberculosis and Autoimmunity.Pathophysiology : the official journal of the International Society for Pathophysiology · 2022
    Review
  12. iScience · 2022
    Article
  13. Pathological and protective roles of dendritic cells inFrontiers in cellular and infection microbiology · 2022
    Review
  14. Review
  15. Article
  16. Article
  17. Advancing Adjuvants forFrontiers in immunology · 2021
    Review
  18. Review
  19. Towards new TB vaccines.Seminars in immunopathology · 2020
    Review
  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

8 authors at 2 institutions in 1 country.

Ranjna Madan-LalaEmory Vaccine Center, Emory University, Atlanta, GA 30329;
Jonathan Kevin Sia
Rebecca King
Toidi Adekambi
Leticia Monin
Shabaana A Khader
Bali Pulendran
Jyothi Rengarajan
Emory University · USUniversity of Pittsburgh · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Understanding the Role of Mucosal Antigen Presenting Cells in Regulating Immune ResponseR37AI048638 · NIAID · STANFORD UNIVERSITY · PI PULENDRAN, BALI · 2009 to 2018
$4.0M
Polarizing T Cell Responses in vivo With Dendritic CellsR37DK057665 · NIDDK · STANFORD UNIVERSITY · PI PULENDRAN, BALI · 2010 to 2019
$3.9M
Innate-adaptive crosstalk in protective and vaccine-induced immunity to TBR01AI134244 · NIAID · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 2017 to 2021
$3.4M
Modulation of Host Responses by Mycobacterium TuberculosisR01AI083366 · NIAID · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 2010 to 2014
$2.2M
Role of Mycobacterium tuberculosis protease in pathogenesis and host responseR00TW008043 · FIC · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 2008 to 2010
$675k
Modulation of Host Responses by Mycobacterium tuberculosisR56AI083366 · NIAID · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 2016 to 2016
$542k
FIC NIH HHS R00 TW008043FIC NIH HHS R00TW008043NCRR NIH HHS P51 RR000165NCRR NIH HHS RR000165NIAID NIH HHS 5R01AI083366-02NIAID NIH HHS R01 AI083366NIAID NIH HHS R01 AI134244NIAID NIH HHS R37 AI048638NIAID NIH HHS R37AI48638NIAID NIH HHS R56 AI083366NIDDK NIH HHS R37 DK057665NIDDK NIH HHS R37DK057665NIH HHS P51 OD011132
6 · The paper itself

Abstract

Mycobacterium tuberculosis is a highly successful human pathogen that primarily resides in host phagocytes, such as macrophages and dendritic cells (DCs), and interferes with their functions. Although multiple strategies used by M. tuberculosis to modulate macrophage responses have been discovered, interactions between M. tuberculosis and DCs are less well understood. DCs are the primary APCs of the immune system and play a central role in linking innate and adaptive immune responses to microbial pathogens. In this study, we show that M. tuberculosis impairs DC cytokine secretion, maturation, and Ag presentation through the cell envelope-associated serine hydrolase, Hip1. Compared to wild-type, a hip1 mutant strain of M. tuberculosis induced enhanced levels of the key Th1-inducing cytokine IL-12, as well as other proinflammatory cytokines (IL-23, IL-6, TNF-α, IL-1β, and IL-18) in DCs via MyD88- and TLR2/9-dependent pathways, indicating that Hip1 restricts optimal DC inflammatory responses. Infection with the hip1 mutant also induced higher levels of MHC class II and costimulatory molecules CD40 and CD86, indicating that M. tuberculosis impairs DC maturation through Hip1. Further, we show that M. tuberculosis promotes suboptimal Ag presentation, as DCs infected with the hip1 mutant showed increased capacity to present Ag to OT-II- and early secreted antigenic target 6-specific transgenic CD4 T cells and enhanced Th1 and Th17 polarization. Overall, these data show that M. tuberculosis impairs DC functions and modulates the nature of Ag-specific T cell responses, with important implications for vaccination strategies.

Indexed as

AnimalsAntigen PresentationDendritic CellsDNA-Binding ProteinsFlow CytometryHumansLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMycobacterium InfectionsMycobacterium tuberculosisDNA-Binding ProteinsHIP1 protein, humanHip1 protein, mouse

Identifiers

PMID24659689
PMCPMC3995873
OpenAlexW1562888755

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.