Evidence map›Paper›PMID 23431344›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2013

Immunomodulation of Homeopathic Thymulin 5CH in a BCG-Induced Granuloma Model.

Leoni Villano Bonamin, Cesar Sato, Ruggero Zalla Neto, Graziela Morante, Thayná Neves Cardoso, Fabiana Rodrigues de Santana, Cideli de Paula Coelho, Lika Osugui, Ana Flavia Popi, Elizabeth Cristina Perez Hurtado and 1 more

Abstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Leoni Villano BonaminResearch Center of Universidade Paulista, Rua Dr. Bacelar 1212, 5th Floor, 04026-002 São Paulo, SP, Brazil ; Laboratory of Veterinary Pathology, Universidade de Santo Amaro, São Paulo, SP, Brazil ; Instituto de Ensino, Pesquisa e Desenvolvimento Royal, São Roque, SP, Brazil.
Cesar Sato
Ruggero Zalla Neto
Graziela Morante
Thayná Neves Cardoso
Fabiana Rodrigues de Santana
Cideli de Paula Coelho
Lika Osugui
Ana Flavia Popi
Elizabeth Cristina Perez Hurtado
Mario Mariano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study analyzed the immune modulation mechanisms of thymulin 5CH in a granuloma experimental model. Male adult Balb/c mice were inoculated with BCG into the footpad to induce granuloma, which was quantitatively evaluated. The phenotypic characterization of phagocyte, T- and B-lymphocyte populations in the peritoneum, and local lymph node was done by flow cytometry. During all experimental periods, thymulin 5CH and vehicle (control) were given ad libitum to mice, diluted into the drinking water (1.6 × 10(-17) M). After 7 days from inoculation, thymulin-treated mice presented reduction in the number of epithelioid cytokeratine-positive cells (P = 0.0001) in the lesion, in relation to young phagocytes. After 21 days, the differentiation of B1 peritoneal stem cells into phagocytes reached the peak, being higher in thymulin-treated mice (P = 0.0001). Simultaneously, the score of infected phagocytes in the lesion decreased (P = 0.001), and the number of B1-derived phagocytes, CD4+ and CD8+ T lymphocytes in the local lymph node increased in relation to control (P = 0.0001). No difference was seen on the CD25+ Treg cells. The results show that thymulin 5CH treatment is able to improve the granuloma inflammatory process and the infection remission, by modulating local and systemic phagocyte differentiation.

Identifiers

PMID23431344
PMCPMC3569925

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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.