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[具体内容]与人类微生物组之间的相互作用 。 你提供的原文不完整,缺少关键信息,我只能按照现有内容翻译到这种程度。请补充完整原文以便我给出更准确的译文。

The Interplay between and Human Microbiome.

作者信息

Nguyen Michelle, Ahn Phillip, Dawi John, Gargaloyan Areg, Kiriaki Anthony, Shou Tiffany, Wu Kevin, Yazdan Kian, Venketaraman Vishwanath

机构信息

College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA 91766, USA.

出版信息

Clin Pract. 2024 Jan 24;14(1):198-213. doi: 10.3390/clinpract14010017.


DOI:10.3390/clinpract14010017
PMID:38391403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10887847/
Abstract

Tuberculosis (TB), a respiratory disease caused by (Mtb), is a significant cause of mortality worldwide. The lung, a breeding ground for Mtb, was once thought to be a sterile environment, but has now been found to host its own profile of microbes. These microbes are critical in the development of the host immune system and can produce metabolites that aid in host defense against various pathogens. Mtb infection as well as antibiotics can shift the microbial profile, causing dysbiosis and dampening the host immune response. Additionally, increasing cases of drug resistant TB have impacted the success rates of the traditional therapies of isoniazid, rifampin, pyrazinamide, and ethambutol. Recent years have produced tremendous research into the human microbiome and its role in contributing to or attenuating disease processes. Potential treatments aimed at altering the gut-lung bacterial axis may offer promising results against drug resistant TB and help mitigate the effects of TB.

摘要

结核病(TB)是由结核分枝杆菌(Mtb)引起的一种呼吸道疾病,是全球范围内导致死亡的一个重要原因。肺部是Mtb的滋生地,曾经被认为是一个无菌环境,但现在已发现其有自身的微生物群落。这些微生物在宿主免疫系统的发育中至关重要,并且可以产生有助于宿主抵御各种病原体的代谢产物。Mtb感染以及抗生素会改变微生物群落,导致生态失调并削弱宿主免疫反应。此外,耐多药结核病病例的增加影响了异烟肼、利福平、吡嗪酰胺和乙胺丁醇等传统疗法的成功率。近年来,对人类微生物组及其在疾病发生或缓解过程中的作用进行了大量研究。旨在改变肠-肺细菌轴的潜在治疗方法可能对耐多药结核病产生有前景的结果,并有助于减轻结核病的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/4c00c942c0df/clinpract-14-00017-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/3881c01b0994/clinpract-14-00017-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/8a6567cf4cd1/clinpract-14-00017-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/fc70ea905a09/clinpract-14-00017-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/4c00c942c0df/clinpract-14-00017-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/3881c01b0994/clinpract-14-00017-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/8a6567cf4cd1/clinpract-14-00017-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/fc70ea905a09/clinpract-14-00017-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/10887847/4c00c942c0df/clinpract-14-00017-g004.jpg

相似文献

[1]
The Interplay between and Human Microbiome.

Clin Pract. 2024-1-24

[2]
Intestinal microbiota disruption limits the isoniazid mediated clearance of Mycobacterium tuberculosis in mice.

Eur J Immunol. 2020-12

[3]
Intestinal dysbiosis compromises alveolar macrophage immunity to Mycobacterium tuberculosis.

Mucosal Immunol. 2019-2-19

[4]
The Dysbiosis Triggered by First-Line Tuberculosis Antibiotics Fails to Reduce Their Bioavailability.

mBio. 2023-4-25

[5]
[Frontier of mycobacterium research--host vs. mycobacterium].

Kekkaku. 2005-9

[6]
, and associates with increased fecal metabolites -4-Hydroxy-L-proline and Genistein in active pulmonary tuberculosis patients during anti-tuberculosis chemotherapy with isoniazid-rifampin-pyrazinamide-ethambutol (HRZE).

Indian J Microbiol. 2022-9

[7]
[Prevalence and transmission of pyrazinamide-resistant in Hunan Province,China].

Zhonghua Jie He He Hu Xi Za Zhi. 2022-7-12

[8]
Prevalence and Drug Resistance Pattern of Isolated from Tuberculosis Patients in Basra, Iraq.

Pol J Microbiol. 2022-5-31

[9]
Treatment of isoniazid-resistant tuberculosis with isoniazid, rifampin, ethambutol, and pyrazinamide for 6 months.

Int J Tuberc Lung Dis. 2002-11

[10]
API TB Consensus Guidelines 2006: Management of pulmonary tuberculosis, extra-pulmonary tuberculosis and tuberculosis in special situations.

J Assoc Physicians India. 2006-3

引用本文的文献

[1]
The Intriguing Connection Between the Gut and Lung Microbiomes.

Pathogens. 2024-11-15

本文引用的文献

[1]
The gut microbiome: A line of defense against tuberculosis development.

Front Cell Infect Microbiol. 2023

[2]
Alterations in the nasopharyngeal microbiota associated with active and latent tuberculosis.

Tuberculosis (Edinb). 2022-9

[3]
The Microbiome as Part of the Contemporary View of Tuberculosis Disease.

Pathogens. 2022-5-16

[4]
Review article: the future of microbiome-based therapeutics.

Aliment Pharmacol Ther. 2022-7

[5]
Barriers to Optimal Tuberculosis Treatment Services at Community Health Centers: A Qualitative Study From a High Prevalent Tuberculosis Country.

Front Pharmacol. 2022-3-25

[6]
The gut microbiota mediates protective immunity against tuberculosis modulation of lncRNA.

Gut Microbes. 2022

[7]
Insights into the Unique Lung Microbiota Profile of Pulmonary Tuberculosis Patients Using Metagenomic Next-Generation Sequencing.

Microbiol Spectr. 2022-2-23

[8]
Respiratory tract infections and gut microbiome modifications: A systematic review.

PLoS One. 2022

[9]
The Role of Gut and Lung Microbiota in Susceptibility to Tuberculosis.

Int J Environ Res Public Health. 2021-11-21

[10]
[A comparative study on the difference of gut microbiota and its biomarkers between patients with pulmonary tuberculosis and healthy controls].

Zhonghua Jie He He Hu Xi Za Zhi. 2021-11-12

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