Evidence map›Paper›PMID 23541388›Full record

ArticleTuberculosis (Edinburgh, Scotland)2013

Immunohistological characterization of spinal TB granulomas from HIV-negative and -positive patients.

S Danaviah, J A Sacks, K P S Kumar, L M Taylor, D A Fallows, T Naicker, T Ndung'u, S Govender, G Kaplan

Abstract read
In one paragraph

Article in Tuberculosis (Edinburgh, Scotland), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Isoliquiritigenin attenuates spinal tuberculosis through inhibiting immune response in a New Zealand white rabbit model.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2018
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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

9 authors at 3 institutions in 1 country.

S DanaviahVirology Laboratory, Africa Centre for Health and Population Studies, Doris Duke Medical Research Institute (DDMRI) at University of KwaZulu-Natal (UKZN), Durban 4013, South Africa. sdanaviah@africacentre.ac.za
J A Sacks
K P S Kumar
L M Taylor
D A Fallows
T Naicker
T Ndung'u
S Govender
G Kaplan
Nelson Mandela Academic Hospital · ZAAfrica Health Research Institute · ZAUniversity of KwaZulu-Natal · ZA

Funding

Emerging XDR-TB: Host and Pathogen ContributionsR01AI080737 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FALLOWS, DOROTHY A. · 2009 to 2013
$2.9M
Analysis of XDR-TB and MDR-TB strains: safety, diagnosis and pathogenesisD43TW008264 · FIC · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KREISWIRTH, BARRY NEAL · 2009 to 2013
$741k
FIC NIH HHS D43 TW008264Howard Hughes Medical InstituteNIAID NIH HHS R01 AI080737
6 · The paper itself

Abstract

Tuberculosis (TB) is mainly a disease of the lungs, but Mycobacterium tuberculosis (Mtb) can establish infection in virtually any organ in the body. Rising rates of extrapulmonary (EP) TB have been largely associated with the HIV epidemic, as patients co-infected with HIV show a four-fold higher risk of EPTB. Spinal TB (Pott's Disease), one of the most debilitating extrapulmonary forms of disease, is difficult to diagnose and can cause deformity and/or neurological deficits. This study examined the histopathology and distribution of immune cells within spinal TB lesions and the impact of HIV on pathogenesis. The overall structure of the spinal granulomas resembled that seen in lung lesions from patients with pulmonary TB. Evidence of efficient macrophage activation and differentiation were detectable within organized structures in the spinal tissue, irrespective of HIV status. Interestingly, the granulomatous architecture and macroscopic features were similar in all samples examined, despite a reversal in the ratio of infiltrating CD4 to CD8 T cells in the lesions from HIV-infected patients. This study provides a foundation to understand the mechanism of tissue destruction and disease progression in Spinal TB, enabling the future development of novel therapeutic strategies and diagnostic approaches for this devastating disease.

Indexed as

AbscessAdolescentAdultAgedAIDS-Related Opportunistic InfectionsBone RemodelingCD4-CD8 RatioCD4 Lymphocyte CountCD8-Positive T-LymphocytesChildFemaleGranulomaHumansMacrophage ActivationMagnetic Resonance ImagingMale

Identifiers

PMID23541388
PMCPMC3681883
OpenAlexW2105761382

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.