alexa Tumoricidal Activation of Macrophages using Jatropha curcas Leaf Extract: As a Proxy for the Treatment of Cancer
ISSN: 1745-7580

Immunome Research
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Research Article

Tumoricidal Activation of Macrophages using Jatropha curcas Leaf Extract: As a Proxy for the Treatment of Cancer

Prayitno A1*, Fitria MS2 and Elmanda AY3

1Department of Pathobiology, Faculty of Medicine, University of Sebelas Maret, Surakarta, Indonesia

2Department of Biology, Faculty of Mathematics and Natural Science, University of Sebelas Maret, Surakarta, Indonesia

3Departemen of Biologi, Faculty of Dentistry, University of Gajah Mada, Yogyakarta, Indonesia

*Corresponding Author:
Prayitno A
Department of Pathobiology, Faculty of Medicine
University of Sebelas Maret, Surakarta, Indonesia
Tel: +62271664178
E-mail: [email protected]

Received date: March 04, 2016; Accepted date: April 28, 2016; Published date: May 09, 2016

Citation: Prayitno A, Fitria MS, Elmanda AY (2016) Tumoricidal Activation of Macrophages using Jatropha curcas Leaf Extract: As a Proxy for the Treatment of Cancer. Immunome Res 12:112. doi:10.4172/1745-7580.10000112

Copyright: © 2016 Prayitno A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



Abstract Background: Jatropha curcas (J. curcas) is a plant rich in methanolic. Macrophages can be activated to become tumoricidal through interactions with immunomodulators. The aim of this study was to investigate the effect of J. curcas leaf extracts on the phagocytic activity of macrophages. Methods: Peritoneal-derived macrophages from male BALB/c mice were obtained using the method of Colligan et al. with some modifications. Latex was added as an antigen to cultures of BALB/c mice macrophages treated with two different concentrations of J. curcas extract and the cultures were observed every 30 minutes for 2 hours. Results: Macrophage latex vacuoles were observed after treatment with 15 μg/mL J. curcas leaf extract, with a mean latex vacuole count of 7.2 vacuoles/cell and a phagocytic index (PI) of 369. Macrophage treatment with 250 μg/mL J. curcas leaf extract produced a mean latex vacuole count of 8.1 vacuoles/cell and a PI of 785. Conclusion: Treatment with J. curcas leaf extracts increased the phagocytic activity of mice macrophages.


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