Therapeutic effects of mesenchymal stem cells on cutaneous leishmaniasis lesions caused by Leishmania major

被引:11
|
作者
Navard, Sahar Hamoon [1 ]
Rezvan, Hossein [1 ]
Haddad, Mohammad Hossein Feiz [2 ,3 ]
Ali, S. A. [4 ]
Nourian, Alireza [1 ]
Eslaminejad, Mohamadreza Baghaban [5 ]
Behmanesh, Mohammad Amin [6 ]
机构
[1] Bu Ali Sina Univ, Sch Vet Sci, Dept Pathobiol, Hamadan, Hamadan, Iran
[2] Dezful Univ Med Sci, Leishmaniasis Dis Registry Comm, Dezful, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Infect & Trop Dis Res Ctr, Hlth Res Inst, Ahvaz, Iran
[4] Nottingham Trent Univ, Interdisciplinary Biomed Res Ctr, Sch Sci & Technol, Nottingham, England
[5] ACECR, Royan Inst Stem Cell Biol & Technol, Dept Stem Cells & Dev Biol, Cell Sci Res Ctr, Tehran, Iran
[6] Dezful Univ Med Sci, Sch Med, Dept Histol, Dezful, Iran
关键词
Cutaneous leishmaniasis; Mesenchymal stem cells; BALB/c; Mice; BONE-MARROW; STROMAL CELLS; DIFFERENTIATION; TRANSPLANTATION; ACTIVATION; RESPONSES;
D O I
10.1016/j.jgar.2020.09.005
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Leishmania major (L. major) is a cutaneous leishmaniasis causative agent. Current chemotherapeutic methods are not totally effective in treatment of this disease. The immunomodulation and tissue repairing capability of mesenchymal stem cells (MSCs), ease of isolation, detection and in vitro culture, have encouraged biologists to use MSCs for cell therapy in different infections such as cutaneous leishmaniasis. Methods: BALB/c mice (6-8 weeks old) were infected with L. major then divided into four groups and treated with MSCs, Glucantime, Glucantime + MSCs, or PBS. Regression of lesions, potency of macrophages for phagocytosis, proliferation of immune cells against Leishmania soluble antigen, reduction of spleen parasite burden and healing of the lesions were evaluated on days 10, 20 and 30 of treatment. Results: The results indicated that the mice intralesionally injected with MSCs showed significant regression in the lesions produced by L. major by day 30. Proliferation of splenocytes stimulated with SLA (soluble leishmania antigen) in vitro in MSC-treated mice on day 20 was significantly higher than in the other groups. The potency of phagocytosis in macrophages of mice treated with MSCs was significantly higher by day 30 and healing of the lesions in this group of mice showed more progress on histopathological examinations. Spleen parasite burden showed significant reduction in the mice treated with Glucantime + MSCs by day 30. Conclusions: The results showed that including MSCs in treatment of cutaneous leishmaniasis caused by L. major is a promising approach. (C) 2020 Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy.
引用
收藏
页码:243 / 250
页数:8
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