TY - JOUR
T1 - The activity of immunoglobulin y anti-Mycobacterium tuberculosis on proliferation and cytokine expression of rat peripheral blood mononuclear cells
AU - Sudjarwo, Sri Agus
AU - Eraiko, Koerniasari
AU - Sudjarwo, Giftania Wardani
AU - Koerniasari,
N1 - Funding Information:
The authors sincerely thank Prof. Drs. H. Muhammad Nasir, M.Si, Ak, Ph.D, the Minister of Research, Technology and Higher Education of the Republic of Indonesia for funding this work
Funding Information:
This study was supported by the Directorate General of Higher Education, Ministry of Research, Technology and Higher Education of the Republic of Indonesia. Grant number: 004/SP2H/LT/DRPM/IV/2017).
Publisher Copyright:
© 2017 Pharmacognosy Research | Published by Wolters Kluwer-Medknow.
PY - 2017/12
Y1 - 2017/12
N2 - Objective: It has long been known that chickens, like mammals, are capable of producing antigen-specific immunoglobulin Y (IgY), which functions similar to IgG. The present study was performed to investigate the activity of IgY anti-Mycobacterium tuberculosis on proliferation, interleukin (IL)-2, and interferon (IFN)-γ expression of rat peripheral blood mononuclear cells (PBMCs). Materials and Methods: The activity of IgY anti-M. tuberculosis in different doses (25, 50, and 100 μg/ml) on rat PBMCs proliferation was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. The production of IL-2 and IFN-γ in the PBMC supernatant was determined using enzyme-linked immunosorbent assay. Investigation was performed on mRNA expression of IL-2 and IFN-γ by reverse transcription-polymerase chain reaction (RT-PCR). Results: IgY anti-M. tuberculosis significantly increased the proliferation of rat PBMC. Furthermore, IgY anti-M. tuberculosis dose dependently increased IL-2 and IFN-γ production in PBMC, suggesting that pharmacological activities of IgY anti-M. tuberculosis in PBMC may be mediated by regulating the production of cytokines. In the RT-PCR, expression of cytokines such as IL-2 and IFN-γ in PBMC cultures was increased by IgY anti-M. tuberculosis. Conclusions: We concluded that increasing IL-2 and IFN-γ productions in PBMC was related to IgY anti-M. tuberculosis, stimulating the mRNA transcription (gene expression) of these cytokines which can induce proliferation of PBMC.
AB - Objective: It has long been known that chickens, like mammals, are capable of producing antigen-specific immunoglobulin Y (IgY), which functions similar to IgG. The present study was performed to investigate the activity of IgY anti-Mycobacterium tuberculosis on proliferation, interleukin (IL)-2, and interferon (IFN)-γ expression of rat peripheral blood mononuclear cells (PBMCs). Materials and Methods: The activity of IgY anti-M. tuberculosis in different doses (25, 50, and 100 μg/ml) on rat PBMCs proliferation was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. The production of IL-2 and IFN-γ in the PBMC supernatant was determined using enzyme-linked immunosorbent assay. Investigation was performed on mRNA expression of IL-2 and IFN-γ by reverse transcription-polymerase chain reaction (RT-PCR). Results: IgY anti-M. tuberculosis significantly increased the proliferation of rat PBMC. Furthermore, IgY anti-M. tuberculosis dose dependently increased IL-2 and IFN-γ production in PBMC, suggesting that pharmacological activities of IgY anti-M. tuberculosis in PBMC may be mediated by regulating the production of cytokines. In the RT-PCR, expression of cytokines such as IL-2 and IFN-γ in PBMC cultures was increased by IgY anti-M. tuberculosis. Conclusions: We concluded that increasing IL-2 and IFN-γ productions in PBMC was related to IgY anti-M. tuberculosis, stimulating the mRNA transcription (gene expression) of these cytokines which can induce proliferation of PBMC.
KW - Immunoglobulin Y anti-Mycobacterium tuberculosis
KW - Interferon-γ
KW - interleukin-2
KW - rat peripheral blood mononuclear cell
UR - http://www.scopus.com/inward/record.url?scp=85042507223&partnerID=8YFLogxK
U2 - 10.4103/pr.pr_66_17
DO - 10.4103/pr.pr_66_17
M3 - Article
AN - SCOPUS:85042507223
SN - 0974-8490
VL - 9
SP - S5-S8
JO - Pharmacognosy Research
JF - Pharmacognosy Research
IS - 5
ER -