Positive Effects of Oral Antibiotic Administration in Murine Chronic Graft-Versus-Host Disease.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
03 Apr 2021
Historique:
received: 26 02 2021
revised: 26 03 2021
accepted: 31 03 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 14 5 2021
Statut: epublish

Résumé

Chronic graft-versus-host disease (cGVHD) is one of the most frequent complications experienced after allogeneic hematopoietic stem cell transplantation. Reportedly, dysbiosis and severe damage to the microbiome are also closely associated with GVHD. Herein, we aimed to elucidate the positive and negative effects of the administration of various antibiotics in a murine model of cGVHD. For allogeneic bone marrow transplantation (allo-BMT), bone marrow from B10.D2 mice were transplanted in BALB/c mice to induce cGVHD. The cGVHD mice were orally administered ampicillin, gentamicin (GM), fradiomycin, vancomycin, or the solvent vehicle (control group). Among the antibiotic-treated mice, the systemic cGVHD phenotypes and ocular cGVHD manifestations were suppressed significantly in GM-treated mice compared to that in control mice. Inflammatory cell infiltration and fibrosis in cGVHD-targeted organs were significantly attenuated in GM-treated mice. Although regulatory T cells were retained at greater levels in GM-treated mice, there were significantly fewer Th17 cells and interleukin (IL)-6-producing macrophages in cGVHD-targeted organs in these mice. Collectively, our results revealed that orally administered GM may exert positive effects in a cGVHD mouse model.

Identifiants

pubmed: 33916809
pii: ijms22073745
doi: 10.3390/ijms22073745
pmc: PMC8038334
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Interleukin-6 0
interleukin-6, mouse 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Shinri Sato (S)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Eisuke Shimizu (E)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Jingliang He (J)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Aier Eye school of Ophthalmology, Central South University, Changsha 410083, China.

Mamoru Ogawa (M)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Kazuki Asai (K)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Hiroyuki Yazu (H)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Department of Ophthalmology, Tsurumi University School of Dental Medicine, Kanagawa 230-0063, Japan.

Robert Rusch (R)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Mio Yamane (M)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Fan Yang (F)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Aier Eye school of Ophthalmology, Central South University, Changsha 410083, China.

Shinji Fukuda (S)

Institute for Advanced Biosciences, Keio University, Yamagata 997-0052, Japan.
Transborder Medical Research Center, University of Tsukuba, Ibaraki 305-8575, Japan.
Intestinal Microbiota Project, Kanagawa Institute of Industrial Science and Technology, Kanagawa 210-0821, Japan.

Yutaka Kawakami (Y)

Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo 160-8582, Japan.
International University of Health and Welfare School of Medicine, Chiba 286-0048, Japan.

Kazuo Tsubota (K)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Yoko Ogawa (Y)

Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.

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Classifications MeSH