Synergic effect of combined xenogeneic mesenchymal stem cells and ceftriaxone on acute septic arthritis

Author:

Sung Pei-Hsun123,Yin Tsung-Cheng45,Chiang John Y67,Chen Chih-Hung8,Huang Chi-Ruei12,Lee Mel S9,Yip Hon-Kan123101112

Affiliation:

1. Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Division of Cardiology, Department of Internal Medicine, , Kaohsiung 833401, Taiwan, ROC

2. Kaohsiung Chang Gung Memorial Hospital Kaohsiung Center for Shockwave Medicine and Tissue Engineering, , Kaohsiung 833401, Taiwan, ROC

3. Kaohsiung Chang Gung Memorial Hospital Kaohsiung Institute for Translational Research in Biomedicine, 833401, Taiwan, ROC

4. Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Department of Orthopedics, , 833401 Kaohsiung, Taiwan, ROC

5. Cheng Shiu University Center for General Education, , Kaohsiung 833301 , Taiwan, ROC

6. National Sun Yat-Sen University Department of Computer Science and Engineering, , Kaohsiung 804201, Taiwan, ROC

7. Kaohsiung Medical University Department of Healthcare Administration and Medical Informatics, , Kaohsiung 807378, Taiwan, ROC

8. Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine Divisions of General Medicine, , Kaohsiung 833401 , Taiwan, ROC

9. Department of Internal Medicine, Paochien Hospital , Pingtung 900068 , Taiwan, ROC

10. Asia University Taichung Department of Nursing,   413305 , Taiwan, ROC

11. China Medical University Department of Medical Research, China Medical University Hospital, , Taichung 404333, Taiwan, ROC

12. Chang Gung University School of Medicine, College of Medicine, , Taoyuan 333323, Taiwan, ROC

Abstract

Abstract Background This study tested the hypothesis that combined ceftriaxone (Cef) and human umbilical cord-derived mesenchymal stem cells (HUCDMSCs) was better than either therapy for alleviating acute septic arthritis (ASA). Methods and results Adult-male C57BL/6 mice were categorized into control group (Clt), group A (ASA only), group B [ASA + Cef (5 mg/kg, IM per day, at days 2 to 16 after ASA induction)], group C [ASA + HUCDMSCs (5 × 105 per mice at days 2, 3, 4 after ASA induction)], and group D (ASA + Cef + HUCDMSCs). Animals were euthanized by day 28. The result demonstrated that the body weight was significantly lower, whereas the ratio of kidney or spleen weight to WB, circulatory WBC count, bacterial colony-formation-unit from circulatory/kidney extraction were significantly higher in group A than in other groups (all P < .001). The proinflammatory cytokines (IL-6/TNF-α) of knee joint fluid were lowest in Clt and significantly and progressively reduced from groups A to D, whereas the circulatory levels of these 2 parameters at the time points of days 3/7/28 exhibited an identical pattern as knee joint fluid among the groups (all P-value < .0001). The scores of vertebral-bone destructions/inflamed synovium were lowest in Clt, highest in group A, significantly higher in group C than in groups B/D, and significantly higher in group C than in group D (all P < .0001). Conclusion Combined antibiotics and Cef and HUCDMSCs was superior to just one therapy for suppressing circulatory and tissue levels of inflammation and knee joint destruction in ASA.

Funder

Chang Gung Memorial Hospital

Chang Gung University

Publisher

Oxford University Press (OUP)

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