Evidence map›Paper›PMID 28000752›Full record

ArticleScientific reports2016

Infergen Stimulated Macrophages Restrict Mycobacterium tuberculosis Growth by Autophagy and Release of Nitric Oxide.

Susanta Pahari, Nargis Khan, Mohammad Aqdas, Shikha Negi, Jagdeep Kaur, Javed N Agrewala

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Different modalities of host cell death and their impact onAmerican journal of physiology. Cell physiology · 2022
    Review
  5. Cumulative Signaling Through NOD-2 and TLR-4 Eliminates theFrontiers in cellular and infection microbiology · 2021
    Article
  6. Innate Lymphoid Cells in Response to Intracellular Pathogens: ProtectionFrontiers in cellular and infection microbiology · 2021
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Curdlan LimitsFrontiers in microbiology · 2019
    Article
  12. Article
  13. Review
  14. Article
  15. 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

6 authors at 2 institutions in 1 country.

Susanta PahariImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, 160036, India.
Nargis KhanImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, 160036, India.
Mohammad AqdasImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, 160036, India.
Shikha NegiImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, 160036, India.
Jagdeep KaurDepartment of Biotechnology, Panjab University, Chandigarh, 160014, India.
Javed N AgrewalaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, 160036, India.
Institute of Microbial Technology · INPanjab University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IFN alfacon-1 (Infergen) is a synthetic form of Interferon (IFN)-α2b. Infergen has immunomodulatory activity and is effective against hepatitis C virus. However, the effect of Infergen (IFG) on Mycobacterium tuberculosis (Mtb) has not yet been reported. Therefore, for the first time, we have studied the influence of IFG in constraining the survival of Mtb in human macrophages. We observed that IFG significantly enhanced the maturation and activation of macrophages. Further, it substantially augmented the secretion of IL-6, nitric oxide (NO) and antigen uptake. Moreover, macrophages exhibited remarkably higher bactericidal activity, as evidenced by reduction in the Mtb growth. Infergen-mediated mechanism was different from the type-1 interferons; since it worked through the activation of NF-κB, phosphorylation of STAT-3 and Akt-PI3K that improved the bactericidal activity through autophagy and NO release. In future, IFG immunotherapy can be a novel strategy for treating patients and controlling TB.

Indexed as

AutophagyB7-1 AntigenB7-2 AntigenCell LineCell ProliferationCytokinesHLA-DR AntigensHumansInterferon-alphaInterleukin-6Leukocytes, MononuclearMacrophagesMicroscopy, ConfocalMycobacterium tuberculosisNitric OxideNitric Oxide Synthase Type IIB7-1 AntigenB7-2 AntigenCD86 protein, humanCytokinesHLA-DR AntigensIL6 protein, humaninterferon alfacon-1Interferon-alphaInterleukin-6Nitric OxideNitric Oxide Synthase Type IINOS2 protein, humanomega-N-MethylarginineRecombinant Proteins

Identifiers

PMID28000752
PMCPMC5175149
OpenAlexW2567388806

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.