The Indonesian Biomedical Journal
Vol 11, No 2 (2019)

beta-Glucan Increases IFN-gamma and IL-12 Production of Peripheral Blood Mononuclear Cells with/without Induction of Mycobacterium tuberculosis Wild-type/Mutant DNA

Meira Erawati (Nursing Department, Faculty of Medicine, Universitas Diponegoro, Jl. Prof. Soedarto, S.H, Tembalang, Semarang)
Nyoman Suci Widyastiti (Faculty of Medicine, Universitas Diponegoro, Jl. Prof. Soedarto, S.H, Tembalang, Semarang)
Tri Indah Winarni (Faculty of Medicine, Universitas Diponegoro, Jl. Prof. Soedarto, S.H, Tembalang, Semarang)
Edi Dharmana (Faculty of Medicine, Universitas Diponegoro, Jl. Prof. Soedarto, S.H, Tembalang, Semarang)



Article Info

Publish Date
01 Aug 2019

Abstract

BACKGROUND: In tuberculosis infections, the immune system is weakened and cannot produce enough cytokines to against the infection. b-glucan is a potent immunomodulator that induces cytokine production in various bacterial infections. This study aimed to determine the effects of b-glucan on the production of interferon (IFN)-γ and interleukin (IL)-12 in peripheral blood mononuclear cells (PBMCs) induced by Mycobacterium tuberculosis DNA.METHODS: PBMCs were isolated from 11 healthy subjects. PBMCs were treated with/without 5 μg/mL b-glucan and M. tuberculosis rpoB wild-type or mutant DNA. The production of IFN-γ and IL-12 in the supernatant was performed with enzyme-linked immune-sorbent assay (ELISA).RESULTS: b-glucan increased significantly (p<0.05) IFN-γ of M. tuberculosis mutant DNA-induced PBMCs, M. tuberculosis wild-type DNA-induced PBMCs, and non-induced PBMCs. b-glucan also increased significantly (p<0.05) IL-12 of M. tuberculosis mutant DNA-induced PBMCs, M. tuberculosis wild-type DNA-induced PBMCs, and non-induced PBMCs. There were not any significant difference between male and female groups for IL-12 and IFN-γ in all treatment groups (p>0.05, ANOVA test).CONCLUSION: This in vitro study indicates that b-glucan increases the performance of PBMCs to produce IFN-γ and IL-12, with/without induction of M. tuberculosis wild-type/ mutant DNA.KEYWORDS: b-glucan, IFN-γ, IL-12, M. tuberculosis, rpoB

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