Evidence map›Paper›PMID 41120888›Full record

ArticleBMC immunology2025

Immunological characteristics and functions of macrophages in Mycobacterium leprae infection.

Xiaodong Zhang, Haiqin Jiang, Weijun Liu, Hongsheng Wang

Abstract read
In one paragraph

Article in BMC immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

4 authors.

Xiaodong ZhangDepartment of Mycobacterium, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology & Hospital for Skin Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, Jiangsu, 210042, China.ORCID 0000-0001-8771-7175
Haiqin JiangDepartment of Mycobacterium, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology & Hospital for Skin Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, Jiangsu, 210042, China.
Weijun LiuDepartment of Mycobacterium, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology & Hospital for Skin Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, Jiangsu, 210042, China.
Hongsheng WangDepartment of Mycobacterium, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology & Hospital for Skin Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, Jiangsu, 210042, China. whs33@vip.sina.com.ORCID 0000-0001-6487-6309

Funding

Jiangsu Provincial Medical Key Laboratory, Jiangsu Province?Capability Improvement Project through Science, Technology and Education ZDXYS202204National Natural Science Foundation of China 81972950, 82173431
6 · The paper itself

Abstract

objectiveOur research aimed to clarify the roles of M1 and M2 macrophages in leprosy, focusing on their polarization states, phagocytic capacities, and the survival of M. leprae within these macrophage subsets.

methodsM1-like macrophages were induced by IFN-γ, IL-4 induced M2-like macrophages, and then they were compared with M. leprae-induced macrophages regarding cell-surface antigen expression and cytokine secretion. The phagocytic capabilities of M1-like and M2-like cells were assessed using a laser-scanning confocal microscope. Simultaneously, their bactericidal capacities were evaluated by 16S rRNA/RLEP qPCR to determine the viability of M. leprae.

resultsM1-like macrophages induced by IFN-γ were characterized by CD86 and CD68 expression and an elevated expression of the IRF-5 gene. In contrast, M2-like macrophages induced by IL-4 were distinguished by enhanced expression of CD163 and CD206 markers and the upregulation of the IRF-4 gene. M. leprae-induced macrophages encompass CD86⁺CD68⁺(M1 markers ) and CD163⁺CD206⁺( M2 markers ) subpopulations, potentially displaying characteristics of both M1-like and M2-like phenotypes. M1-like macrophages secreted Th1 cytokines, including IL-1β, IL-6, IL-15, and TNF-α, whereas M2-like macrophages secreted IL-10 and TGF-β. At different stages, macrophages induced by M. leprae released Th1 and Th2 cytokines. The phagocytic ability of M2-like macrophages exceeded that of M1-like macrophages. Nevertheless, M. leprae viability was notably higher in M2-like macrophages, indicating a weaker sterilizing capacity than in M1-like macrophages. Conversely, M1-like macrophages demonstrated potent bactericidal activity, although their phagocytic ability was relatively lower than that of M2-like macrophages.

conclusionOur findings suggested the notable significance of macrophage polarization in leprosy. M1 macrophages exhibited a relatively strong bactericidal effect against M. leprae, while M2 macrophages might have been somewhat associated with pathogen persistence.

Indexed as

LeprosyMacrophagesMycobacterium lepraeAnimalsAntigens, CDCells, CulturedCytokinesHumansInterferon-gammaInterleukin-4Macrophage ActivationPhagocytosisAntigens, CDCytokinesInterferon-gammaInterleukin-4LeprosyM1 macrophagesM2 macrophagesMacrophage polarizationMycobacterium leprae

Identifiers

PMID41120888
PMCPMC12538733

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Registered trials

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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.