• 한국가금학회:학술대회논문집
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• 한국가금학회 2003년도 제20차 정기총회 및 학술발표회
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• pp.82-83
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• 2003

크릴밀 사료가 육계병아리의 생산성을 감소시키는 경향을 완화하기 위하여 항산화작용이 있은 콩추출물이 함유된 크릴밀을 급여하여 육계병아리의 생산성을 조사하고, 파두유의 피하주입으로 급성기반응을 발생시켜 비장세표와 PBMC 증식도, 그리고 TNF-$\alpha$와 Ovotranferrin의 발현에 미치는 콩 추출물 함유 크릴밀 사료의 영향을 조사하였다. 육계 병아리에서 콩 추출물 함유 크릴밀 사료는 생산성을 증가시켰다. 급성기 반응시 콩 추출물 함유 크릴밀 사료는 비장세포의 증식도를 낮추나 PBMC의 증식조는 높았다. 혈장내 순환 TNF-$\alpha$와 Ovotranferrin의 농도는 콩 추출물 함유 크릴밀 사료 급여로 감소하였다. 본 성적은 콩 추출물 함유 크릴밀 사료가 육계 병아리의 급성기 반응에 관여하고 있다는 것을 나타내었다.

• 한국가금학회:학술대회논문집
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• 한국가금학회 2005년도 제22차 정기총회 및 학술발표회
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• pp.76-77
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• 2005

사멸 살모넬라와 뱅코마이신 첨가 사료가 Salmonella typhimurium을 감염시킨 육계 병아리의 생산성과 면역계 및 항산화계에 미치는 영향을 조사하였다. 살모넬라 인공 감염전(27일)에는 육계 병아리의 생산성은 사료에 따른 유의한 영향이 없었다. 항산화계에서 사멸 살모넬라와 뱅코마이신 첨가 사료가 기초사료에 비하여 적혈구 세포액내 MnSOD 활성을 낮추었다. 살모넬라 인공 감염 7일후 육계 병아리의 생산성은 사멸 살모넬라와 뱅코마이신 첨가 사료가 대조감염구에 비하여 높은 일당증체량과 사료효율을 나타냈다. 살모넬라 인공 감염 7일후 및 15일후 사멸 살모넬라와 뱅코마이신 첨가 사료가 대조감염구에 비하여 적혈구 세포내 과산화물 분해효소의 활성을 낮춘 반면, LPS 자극에 의한 PBMC 증식도와 PBMC 증식에 분비된 IL-1수준을 높였다. 본 성적은 사료중 사멸 살모넬라와 뱅코마이신 첨가가 살모넬라 감염 육계 병아리 생산성 증가에 영향을 미쳤으며, 이는 항산화 효소계와 PBMC 증식도, IL-1 분비 및 혈장 TNF-a농도 등 타고난 면역계에 의한 것으로 생각된다.

• 대한수의학회지
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• 제42권2호
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• pp.209-217
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• 2002

This study was performed to produce monoclonal antibodies (mAb) specifically reacting with chicken leukocyte surface antigens. Popliteal lymph node cells of BALB/c mice previously immunized through foot-pad with peripheral blood mononuclear cells (PBMC) of chickens separated by Ficoll-Histopaque method. They were fused with P3X63Ag14 mouse myeloma cells. A total of 34 hybridomas secreted antibodies specifically binding to the PBMC. According to the reactivity patterns with PBMC, the mAbs were divided into 4 groups. Group 1 mAbs (IIB3, IIB10, IIE10) specifically reacted with non-adherent lymphocytes but not with adherent cells which were mainly composed of thrombocytes and monocytes in PBMC culture. These mAbs were reactive with 25-59% of thymus cells and 42-64% of spleen cells of chickens. They did not show any significant reactivity with cells in the bursa of Fabricius, T-cell (MDCC-MSB1) and B-cell (LSCC-1104B1) lines. These results indicate that Group I mAbs specifically reacted with T-lymphocyte subpopulation. Monoclonal antibodies in Group II (IC6, IG2-2 and IID9) showed specific reactivity with monocytes but not with thrombocytes or non-adherent cells in PBMC culture. These mAbs, though not reacted with the chicken macrophage cell line, HD11, also bound to macrophages of the spleen and lung in immunohistochemical staining. Five mAbs in Group III showed characteristics of binding to lymphocytes and monocytes, but not to thrombocytes. Twenty-three mAbs in Group IV showed specific reactivity to lymphocytes, monocytes, and thrombocytes. Two mAbs (IC3 and IE9) in Group IV reacted with most of PBMC.

• Asian-Australasian Journal of Animal Sciences
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• 제27권4호
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• pp.471-478
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• 2014

Investigating gene expression of immune cells of whole blood or peripheral blood mononuclear cells (PBMC) under polyinosinic:polycytidylic acid (poly I:C) stimulation is valuable for understanding the immune response of organism to RNA viruses. Quantitative real-time PCR (qRT-PCR) is a standard method for quantification of gene expression studies. However, the reliability of qRT-PCR data critically depends on proper selection of reference genes. In the study, using two different analysis programs, geNorm and NormFinder, we systematically evaluated the gene expression stability of six candidate reference genes (GAPDH, ACTB, B2M, RPL4, TBP, and PPIA) in samples of whole blood and PBMC with or without poly I:C stimulation. Generally, the six candidate genes performed a similar trend of expression stability in the samples of whole blood and PBMC, but more stably expressed in whole blood than in PBMC. geNorm ranked B2M and PPIA as the best combination for gene expression normalization, while according to NormFinder, TBP was ranked as the most stable reference gene, followed by B2M and PPIA. Comprehensively considering the results from the two programs, we recommended using the geometric mean of the three genes, TBP, PPIA and B2M, to normalize the gene expression of whole blood and PBMC with poly I:C stimulation. Our study is the first detailed survey of the gene expression stability in whole blood and PBMC with or without poly I:C stimulation and should be helpful for investigating the molecular mechanism involved in porcine whole blood and PBMC in response to poly I:C stimulation.

• Tuberculosis and Respiratory Diseases
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• 제57권4호
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• pp.336-344
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• 2004

연구배경 : 폐암에 대한 거의 대부분의 면역 치료는 실패하였는데, 이는 폐암 자체에 존재하는 면역 억제 기전을 극복하지 못한데 기인하는 것으로 판단된다. Uteroglobin (UG, CCSP)은 항염증 등의 활성을 보인다. 방 법 : A549에 Ad-UG을 처리하고, 상층액의 $PGE_2$ 농도를 측정하였다. RPMI 1640, A549 배양액과 UG 혹은 COX-2 억제제인 NS-398을 처리 후 얻은 폐암세포주 상층액으로 PBMC를 배양 후 Th 1 type cytokines과 Th 2 type cytokines의 농도를 측정하였다. 결 과 : $PGE_2$는 UG이 발현되는 세포주에서 감소하였다. 폐암 세포 배양 배지로 키운 면역 세포의 cytokines가 증가하는 양상을 보였으나, UG등을 처리한 비소세포 폐암주의 배양액은 PBMC의 면역 반응을 정상적으로 유도하였다. 결 론 : 비소세포폐암주 배양액은 PBMC의 면역 반응을 비정상적으로 유도하지만, UG은 $PGE_2$의 분비를 억제함으로써, PBMC의 면역 반응을 강화시킨다.

• Food Science and Biotechnology
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• 제17권3호
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• pp.631-636
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• 2008

Acanthopanax divaricatus var. albeofructus (ADA) have been shown to have various levels of activity such as antioxidant, anticancer, antivirus, and immunostimulatory effects. However, little is known about its mechanism related to the modulation of immune activities. In this study, a water extract of ADA leaves were used to treat human peripheral blood mononuclear cells (hPBMC) to determine the underlying mechanisms for the immunostimulatory effects. To characterize its immunomodulatory activity, the secretion level of various cytokines including IL-2, IL-4, IL-6, IL-10, IL-12, IFN-$\gamma$, and TNF-$\alpha$ were measured using enzyme-linked immunosorbent assay (ELISA). Treatment of hPBMC with ADA leaf extract in an in vitro experiment induced various Th1 cytokines in a dose-dependent manner. A significant increase of IL-2, IL-12, IFN-$\gamma$, and TNF-$\alpha$ secretion was observed in the presence of ADA leaf extract. In contrast, Th2 cytokines including IL-4 and IL-6 were suppressed. There was no significant change in IL-10 release. Our results showed an increase in Th1 and a decrease in Th2 cytokine secretion which suggests that ADA may influence the immune response towards a predominance of Th1 cytokines in the immune system.

• 대한한의학회지
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• 제22권1호
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• pp.53-62
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• 2001

Objective : The aim of this study was to evaluate the efficacy of Injinchunggan-tang on Hepatitis C virus infection, and to clarify the mechanism of treatment by indentifying the effect of Injinchunggan-tang on cytokine secretion. Methods : In vitro model of HCV infection in MOLT 4 cell was used. The effect of Injinchunggan-tang on the attachment of HCV on MOLT 4 cell was studied by PCR method. The change of cytokine secretion according to Injinchunggan-tang treatment was investigated by ELISA. Results : Injinchunggan-tang inhibited the attachment of HCV on MOLT 4 in the concentration of $10-2{\mu\textrm{g}}/\mu\textrm{\ell}$ and $10-1{\mu\textrm{g}}/\mu\textrm{\ell}$. In cytokine assay, Injinchunggan-tang increased the secretion of IL-4 of mouse splenocytes and PBMC in 48 hour culture as well as the secretion of IL-12 of mouse splenocytes and PBMC in 48 hour culture, whereas it decreased the secretion of $IFN-{\gamma}$ of mouse splenocytes in 24 and 48 hour culture. Conclusion : The results of this study show that Injinchunggan-tang has an inhibitory effect on the attachment on HCV on Mo1t4 Cell, and that it increases the secretion of IL-4 and IL-12 of mouse splenocyte and PBMC.

• Archives of Pharmacal Research
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• 제28권5호
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• pp.573-581
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• 2005

Flavonoids, a group of low molecular weight phenylbenzopyrones, have various pharmacological properties including antioxidant activity, anticancer, and immunomodulatory effects. In the present study, lipopolysaccharide (LPS) and phorbol 12-myristate 13-acetate/phytohemagglutinin (PMA/PHA) were used as stimulants for RAW 264.7 macrophages and human peripheral blood mononuclear cell (hPBMC), and tumor necrosis factor (TNF)-${\alpha}$ and interleukin (IL)-2 productions were measured. In addition, flavonoids were examined for their effects on LPS-induced NO production in RAW 264.7 macrophages. The results showed that all compounds were not strongly cytotoxic at the tested concentrations on hPBMC and RAW 264.7 macrophages. On immunomodulatory properties, catechin, epigallocatechin (EGC), naringenin, and fisetin repressed NO production and TNF-${\alpha}$ secretion. Furthermore, catechin, epigallocatechin gallate (EGCG), epicatechin (EC), luteolin, chrysin, quercetin, and galangin increased IL-2 secretion while EGC, apigenin, and fisetin inhibited the secretion. These results indicated that flavonoids have the capacity to modulate the immune response and have a potential anti-inflammatory activity. There was no obvious structure-activity relationship regard to the chemical composition of the flavonoids and their cell biological effects.

• 한국가금학회:학술대회논문집
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• 한국가금학회 2005년도 제22차 정기총회 및 학술발표회
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• pp.78-79
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• 2005

젖당 또는 사멸 살모넬라 첨가 사료가 Salmonella typhimurium을 감염시킨 육계 병아리의 생산성과 면역반응에 미치는 영향을 조사하였다. 젖당 사료는 3주령 육계 병아리의 생산성을 감소시켰고, 혈장 과산화물 분해 효소와 IL-1의 농도는 젖당과 살모넬라 사료에 의해서 증가되었다. 살모넬라 인공 감염 7일 후의 육계 병아리에서 비감염구에 비해 증체 및 사료효율, 혈장 과산화물 분해 효소 활성, 적혈구 세포액의 MnSOD 활성도 증가하였다. 감염후 15일이 지난 육계 병아리에서 사료효율은 젖당 또는 사멸 살모넬라 사료 그리고 살모넬라감염의 영향을 받지 않았다. 혈장 과산화물 분해효소, MnSOD 활성과 LPS자극 PBMC의 증식도는 젖당과 사멸 살모넬라 급여구에서 감염 대조군보다 높았다. IL-1의 수준은 사멸 살모넬라 사료에서 유의하게 높았다. 본성적은 젖당과 사멸 살모넬라 급여는 살모넬라 감염 육계 병아리의 PBMC의 증식과 IL-1의 분비를 증가시키고, SOD 활성을 변화시켜 타고난 면역계를 조정한다는 것을 나타내었다.

• 생약학회지
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• 제37권4호
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• pp.221-228
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• 2006

A lectin was purified from Serrognathus platymelus castanicolor larvae and named as SPL. The purification was carried out by ion-exchange chromatography on DEAE Sephadex A-50 and gel filtration chromatography on Sephadex G-200. The purity of the protein was verified by polyacrylamide gel electrophoresis and the purified lectin agglutinated erythrocytes of rabbit and human A, B, O, AB. SPL was tested it's ability to enhance the expressions of cytokines, $IL-1\alpha$, IL-2, IL-6, $TNF\alpha$ and $IFN\gamma$ by human peripheral blood mononuclear cells (PBMC) obtained from healthy donors. mRNA analyses were performed by RT-PCR at the moment of 1, 4, 8, 24, 48, 72 and 96 h after stimulation of PBMC with purified SPL. The patterns of IL-2 band were slightly expressed from 24 h and the strongest band was appeared at 96 h. The expressions of $IL-1\alpha$ and IL-6 mRNA were strong from 1 to 8 h and those of $TNF\alpha$ were from 48 to 96 h. The mRNA encoding $IFN\gamma$ were not detected. The addition of SPL for macrophage cultures induced production of nitric oxide (NO) by cells in a dose-dependent manner. NO release was partially inhibited by $TNF\alpha$ antibodies. These results suggest that SPL has the ability to enhance cytokine expressions in PBMC and to induce the NO release by TNFa in macrophage cultures from PBMC cultures.