Evidence map›Paper›PMID 18443098›Full record

ArticleInfection and immunity2008

The phenolic glycolipid of Mycobacterium tuberculosis differentially modulates the early host cytokine response but does not in itself confer hypervirulence.

Daniel Sinsimer, Gaelle Huet, Claudia Manca, Liana Tsenova, Mi-Sun Koo, Natalia Kurepina, Bavesh Kana, Barun Mathema, Salvatore A E Marras, Barry N Kreiswirth and 2 more

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 135 citations in OpenAlex.

  1. Delayed-Type Hypersensitivity toInternational journal of molecular sciences · 2026
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Drug-resistant strains ofFrontiers in cellular and infection microbiology · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. PPE38-Secretion-Dependent Proteins ofFrontiers in immunology · 2021
    Article
  14. Review
  15. Review
  16. Immunology ofMicrobiology spectrum · 2019
    Review
  17. Article
  18. Article
  19. Review
  20. Underestimated Manipulative Roles ofFrontiers in immunology · 2019
    Review

8 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

12 authors at 3 institutions in 2 countries.

Daniel SinsimerLaboratory of Mycobacterial Immunity and Pathogenesis, Public Health Research Institute Center, University of Medicine and Dentistry of New Jersey, 225 Warren St., Newark, NJ 07103, USA.
Gaelle Huet
Claudia Manca
Liana Tsenova
Mi-Sun Koo
Natalia Kurepina
Bavesh Kana
Barun Mathema
Salvatore A E Marras
Barry N Kreiswirth
Christophe Guilhot
Gilla Kaplan
Immunité et Cancer · FRInstitut de Pharmacologie et de Biologie Structurale · FRUniversity of the Witwatersrand · ZA

Funding

Host &Pathogen Determinants of M tuberculosis LatencyR01AI054338 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KAPLAN, GILLA · 2002 to 2011
$5.0M
Host-Pathogen Interactions and M.tb Drug ResistanceR01AI066046 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KAPLAN, GILLA · 2006 to 2009
$1.3M
NIAID NIH HHS AI66046NIAID NIH HHS R01 AI054338NIAID NIH HHS R01 AI066046
6 · The paper itself

Abstract

Mycobacterium tuberculosis possesses a diversity of potential virulence factors including complex branched lipids such as the phenolic glycolipid PGL-tb. PGL-tb expression by the clinical M. tuberculosis isolate HN878 has been associated with a less efficient Th1 response and increased virulence in mice and rabbits. It has been suggested that the W-Beijing family is the only group of M. tuberculosis strains with an intact pks1-15 gene, required for the synthesis of PGL-tb and capable of producing PGL-tb. We have found that some strains with an intact pks1-15 do not produce PGL-tb while others may produce a variant of PGL-tb. We examined the early host cytokine response to infection with these strains in vitro to better understand the effect of PGL-tb synthesis on immune responses. In addition, we generated a PGL-tb-producing H37Rv in order to determine the effect of PGL-tb production on the host immune response during infection by a strain normally devoid of PGL-tb synthesis. We observed that PGL-tb production by clinical M. tuberculosis isolates affected cytokine production differently depending on the background of the strain. Importantly, while ectopic PGL-tb production by H37Rv suppressed the induction of several pro- and anti-inflammatory cytokines in vitro in human monocytes, it did not lead to increased virulence in infected mice and rabbits. Collectively, our data indicate that, while PGL-tb may play a role in the immunogenicity and/or virulence of M. tuberculosis, it probably acts in concert with other bacterial factors which seem to be dependent on the background of the strain.

Indexed as

AnimalsAntigens, BacterialCells, CulturedCytokinesGlycolipidsHumansLeukocytes, MononuclearMiceMonocytesMycobacterium tuberculosisRabbitsSpecies SpecificityTuberculosis, PulmonaryVirulenceAntigens, BacterialCytokinesGlycolipidsphenolic glycolipid I, Mycobacterium leprae

Identifiers

PMID18443098
PMCPMC2446685
OpenAlexW2157179706

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.