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

Stem Cells Transl Med. 2024 Aug 16;13(8):724-737. doi: 10.1093/stcltm/szae034.

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.

Keywords: acute sepsis arthritis; inflammation; knee joint; vertebral destruction.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Arthritis, Infectious* / drug therapy
  • Arthritis, Infectious* / therapy
  • Ceftriaxone* / pharmacology
  • Humans
  • Male
  • Mesenchymal Stem Cell Transplantation* / methods
  • Mesenchymal Stem Cells* / metabolism
  • Mice
  • Mice, Inbred C57BL*

Substances

  • Ceftriaxone
  • Anti-Bacterial Agents