Bone marrow-derived mesenchymal stem cell (BM-MSC): A tool of cell therapy in hydatid experimentally infected rats

IF 4 Q2 CELL & TISSUE ENGINEERING
Faten A.M. Abo-Aziza , Abdel Kader A. Zaki , Amal M. Abo El-Maaty
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引用次数: 16

Abstract

This study aimed to clarify the potentiality of bone marrow mesenchymal stem cells (BM-MSC) transplantation with albendazole (ABZ) on the modulation of immune responses against hydatid cyst antigens and the regeneration of injured livers in experimentally infected rats. Three different antigens of hydatid cyst fluid (HCF), hydatid cyst protoscolex (HCP) and hydatid cyst germinal layer (HCG) were isolated and their antigenic potencies were determined. The ultrasound, immunological and pathological criteria were investigated. Counting of 80% confluence BM-MSC was 4.68 × 104 cells/cm2 with 92.24% viability. Final population doublings score was 65.31 that indicated proliferation and self-renewability. Phenotyping of BM-MSC showed expression of CD73 and CD29 without exhibition of CD34 and CD14. Ultrasound examination showed multiple hydatid cysts in liver with low blood flow and spleenomegaly 8 weeks’ post infection. No significant differences were noted in cystic diameter in uni-cyst liver at 2nd and 4th weeks following ABZ treatment while it was significantly decreased (P < 0.05) following transplantation of BM-MSC + ABZ treatment comparing to experimentally infected untreated group. Igs and IgG responses to the three antigens were significantly elevated while elevation in IgM response was only to HCG (P < 0.05). ABZ treatment accompanied with significant decrease in Igs and IgG titers against HCF and HCG only at 4th week post treatment (P < 0.05). However, Igs titer against HCF, HCP and HCG was significantly decreased at the 4th week following transplantation of BM-MSC + ABZ. Interestingly, the combination of BM-MSC + ABZ treatment resulted in reduction of Igs response to HCP to normal level as that of healthy control. Experimental infection resulted in elevation of TNF-α and IL-6 (P < 0.05) while, IL-4 and IL-10 decreased (P < 0.01). After transplantation of BM-MSC + ABZ treatment, serum TNF-α and IL-6 concentrations were reduced (P < 0.05) at both the 2nd and 4th weeks. However, IL-4 and IL-10 concentrations were significantly elevated (P < 0.05) only at 4th week following transplantation of BM-MSC + ABZ treatment. In conclusion, BM-MSC transplantation following ABZ administration can regenerate injured liver tissue without complete disappearance of hydatid cyst. In addition, it can modulate host protective humeral and cell mediated immune responses against hydatid cyst antigens. Therefore, the current study encourages to move to the step of performing clinical trials in humans.

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骨髓源间充质干细胞(BM-MSC):包虫实验感染大鼠的细胞治疗工具
本研究旨在阐明阿苯达唑(ABZ)联合骨髓间充质干细胞(BM-MSC)移植对实验性感染大鼠对包虫病抗原的免疫应答调节和损伤肝脏再生的潜力。分离了包囊液(HCF)、包囊原头节(HCP)和包囊生发层(HCG) 3种不同抗原,并测定了它们的抗原性。进行超声、免疫及病理检查。80%合流BM-MSC计数为4.68 × 104个/cm2,存活率为92.24%。最终群体加倍得分为65.31,表明增殖和自我再生能力。BM-MSC表型分析显示CD73和CD29表达,CD34和CD14不表达。感染后8周超声检查示肝脏多发包虫病,血流量低,脾肿大。在ABZ治疗后第2周和第4周,单囊肿性肝脏的囊直径无显著差异,但明显降低(P <0.05),与实验感染未治疗组比较。IgG和IgG对三种抗原的反应均显著升高,而IgM反应仅对HCG升高(P <0.05)。ABZ治疗仅在治疗后第4周伴抗HCF和HCG的IgG和IgG滴度显著下降(P <0.05)。然而,在移植BM-MSC + ABZ后第4周,igg对HCF、HCP和HCG的滴度显著降低。有趣的是,BM-MSC + ABZ联合治疗导致Igs对HCP的反应降低到正常水平,与健康对照组相比。实验性感染导致TNF-α和IL-6升高(P <0.05), IL-4、IL-10降低(P <0.01)。移植BM-MSC + ABZ治疗后,血清TNF-α和IL-6浓度降低(P <0.05)。然而,IL-4和IL-10浓度显著升高(P <0.05),仅在移植后第4周出现。综上所述,ABZ给药后BM-MSC移植可使损伤肝组织再生,而包虫病不完全消失。此外,它可以调节宿主保护性肱骨和细胞介导的免疫应答,以对抗包虫抗原。因此,目前的研究鼓励进行人体临床试验的步骤。
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来源期刊
Cell Regeneration
Cell Regeneration Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
5.80
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Cell Regeneration aims to provide a worldwide platform for researches on stem cells and regenerative biology to develop basic science and to foster its clinical translation in medicine. Cell Regeneration welcomes reports on novel discoveries, theories, methods, technologies, and products in the field of stem cells and regenerative research, the journal is interested, but not limited to the following topics: ◎ Embryonic stem cells ◎ Induced pluripotent stem cells ◎ Tissue-specific stem cells ◎ Tissue or organ regeneration ◎ Methodology ◎ Biomaterials and regeneration ◎ Clinical translation or application in medicine
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