• Parasites, Hosts and Diseases
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• 제30권1호
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• pp.43-48
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• 1992

폐흡충(Paragonimus westermani) 피낭유충을 마우스에 감염시킨 후 in vitro상에서 비장 림프구에 폐흡충 항원, phytohemagglutinin(PHA) 및 혈청 첨가시 림프구 아세포화 반응을 관찰하였다. PHA로 자극시킨 감염 마우스의 비장 림프구는 비감염군에 비해 감염 1 주 후에 평균 53.6%의 유의한 증식 억제를 관찰하였고, 폐흡충 성충항원으로 자극시킨 경우 감염 마우스의 비장 림프구의 증식은 감염 1 주 후부터 6 주까지 비감염군에 비해 중가되었으며 특히 감염 1 주와 4 주 후에는 각각 평균 200.9% 및 280.2%의 유의한 수준으로 증가되었다. 또한 피낭유충 항원으로 감염 마우스의 비장 림프구를 자극시에도 비감염군의 림프구의 증식에 비해 전반적으로 증가되었으며 특히 감염 4 주 째에는 평균 180.5%의 유의한 수준으로 증가하였다. 폐홉충에 감염된 마우스의 감염 4 주 째 혈청을 PHA로 자극시킨 비감염 마우스 비장 림프구에 첨가하였을 때 유의한 수준의 증식의 억제를 관찰하였다. 이러한 결과들로 보아 폐흡충 감염 마우스에서 림프구가 세포 매개성 면역에 관여하며 감염 혈청이 PHA에 대한 T 림프구의 증식을 억제함을 알 수 있었다.

• Journal of Periodontal and Implant Science
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• 제26권3호
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• pp.641-654
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• 1996

In infectious disease, invasion of host tissue by bacteria or their products frequently induces a wide variety of inflammatory and immunopathologic reaction. Evidence indicates that cytokines are involved in the initiation and progression of chronic inflammatory diseases, such as periodontitis. Interleukin-6, which is a multifunctional cytokine, has important roles in acute and chronic inflammation and may also be implicated in bone resorption. Periodontal diseases are characterized by chronic inflammation of the periodontium with alveolar bone resoption. A principal driving force behind this response appears to lie in the immune system's response to bacteria. Many of the cell components which have been shown to function as virulence factors in gram-negative bacteria are associated with the bacterial surface. Of these, lipopolysaccharide has been characterized as one that mediates a number of biological activities which can lead to the destruction of host tissue. Non-steroidal antiinflammatory drug is used for reduce inflammation, and most of NSAIDs inhibit prostaglandine $E_2$ production, but it is shown that $PGE_2$ production is stimulated by IL-1 in recent study. So, the influence of other cytokines except $PGE_2$ on periodontium can not be avoided. Therefore, new antiinflammatory drug is needed. Rhizoma coptidis is used in oriental medicine for anti-inflammation and antiseptics. In this present study, we examined the IL-6 release in periodontal ligament cells treated with the lipopolysaccharide, and also the effect of rhizoma coptidis on cellular activity and IL-6 production of periodontal ligament cells. To evaluate the effect of rhizoma coptidis on cellular activity, the cells were seeded at a cell density of $1{\times}10^4$ cells/well in 24-well culture plates. After one day incubation, 1-6, 10-9 and 10-12 g/ml of rhizoma coptidis and 5, $10{\mu}g/ml$ of LPS were added to the each well and incubated for 1 and 2 days, respectively. Then, MTT assay were carried out. To evaluate the effect of rhizoma coptidis on IL-6 production, the cells were seeded at a cell density of $1.5{\times}10^4$ cells/well in 24-well culture plates. After one day incubation, 10-9 g/ml of rhizoma coptidis and 5, $10{\mu}g/ml$ of LPS were added to the each well and incubated for 3, 6, 12 and 24 hours. Then, amounts of IL-6 production is measured by IL-6 ELISA kit used. The results were as follows : 1. Rhizoma coptidisrbelow to ($10^{-6}g/ml$) significantly increaed cellular activity of periodontal ligament cells than control. 2. Rhizoma coptidist ($10^{-9}g/ml$) significantly increased cellular activity of LPS($5{\mu}g/ml$)-treated periodontal ligament cells than control. 3. LPS(5 and $10{\mu}g/ml$) significantly increased IL-6 production of periodontal ligament cells than control. 4. Rhizoma coptidis($10^{-9}g/ml$) decreased IL-6 production of LPS ($5{\mu}g/ml$)-treated periodontal.ligarnent cells than LPS only tested group. These findings suggest that stimulation of the IL-6 release of periodontal ligament cells by LPS may have a role in the progression of inflammation and alveolar bone resoption in periodontal disease, and that inhibition of the IL-6 release of cells and stimulation of cellular activity by rhizoma coptidis may help the periodontal regeneration.

• 한국식품영양과학회지
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• 제45권2호
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• pp.174-180
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• 2016

본 연구에서는 산양유 발효유(F-GM)의 급여가 면역 활성과 체력증진에 미치는 영향을 조사하였다. F-GM을 경구 투여한 마우스의 비장세포는 림프구 유사분열 촉진인자인 ConA와 LPS에 대한 증식반응의 상승을 나타내었다. ConA를 처리한 비장세포로부터 분비되는 cytokine을 ELISA법에 의해 정량한 결과 F-GM 투여에 의해 IL-2와 IFN-${\gamma}$의 생성은 유의하게 증가하였으나, IL-4 및 IL-10의 생성은 별다른 변화를 보이지 않았다. 또한 RT-PCR을 이용한 이들 cytokine mRNA의 정량실험에서도 F-GM 투여로 IL-2와 IFN-${\gamma}$의 mRNA가 증가하는 것을 확인하였다. 한편 KLH(20 mg/mouse)를 정상 대조군 마우스 혹은 F-GM을 급이한 마우스에 각각 면역하고 5주째에 KLH에 대한 항체가를 측정한 결과 F-GM을 급이한 마우스에서 항체가가 유의하게 상승하는 것으로 나타났다. KLH에 대한 항체의 isotype을 조사한 실험에서는 KLH에 대한 IgG1, IgG2a 그리고 IgM 특이항체의 상승이 관찰되었다. F-GM 경구 투여가 세포성 면역에 미치는 영향을 측정하기 위하여 면역개시 7주째의 마우스를 이용하여 KLH에 대한 지연형 과민반응(DTH)을 측정하였다. 그 결과 F-GM을 경구 투여한 마우스에서 DTH의 유의한 상승효과가 확인되었다. 한편 수영시험을 통해 F-GM의 경구 투여가 체력증강에 미치는 영향을 측정한 결과 F-GM을 투여한 마우스에서 매우 유의한 수영시간의 연장 효과가 관찰되었다. 이들 결과로부터 F-GM은 면역세포의 활성화를 통한 면역력 강화는 물론 체력을 증가시키는 생리활성을 갖는 것으로 확인되었다.

• Journal of Ginseng Research
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• 제44권4호
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• pp.580-592
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• 2020

Background: Radix et Rhizoma Ginseng (thereafter called ginseng) has been used as a medicinal herb for thousands of years to maintain people's physical vitality and is also a non-organ-specific cancer preventive and therapeutic traditional medicine in several epidemiologic and preclinical studies. Owing to few toxic side effects and strong enhancement on body immunity, ginseng has admirable application potential and value in cancer chemoprevention. The study aims at investigating the chemopreventive effects of ginseng on cutaneous carcinoma and the underlying mechanisms. Methods: The mouse skin cancer model was induced by 7,12-dimethylbenz[a]anthracene/12-O-tetradecanoylphorbol-13-acetate. Ultraperformance liquid chromatography/mass spectrometry was used for identifying various ginsenosides, the main active ingredients of ginseng. Comprehensive approaches (including network pharmacology, bioinformatics, and experimental verification) were used to explore the potential targets of ginseng. Results: Ginseng treatment inhibited cutaneous carcinoma in terms of initiation and promotion. The content of Rb1, Rb2, Rc, and Rd ginsenosides was the highest in both mouse blood and skin tissues. Ginseng and its active components well maintained the redox homeostasis and modulated the immune response in the model. Specifically, ginseng treatment inhibited the initiation of skin cancer by enhancing T-cell-mediated immune response through upregulating HSP27 expression and inhibited the promotion of skin cancer by maintaining cellular redox homeostasis through promoting nuclear translocation of Nrf2. Conclusion: According to the study results, ginseng can be potentially used for cutaneous carcinoma as a chemopreventive agent by enhancing cell-mediated immunity and maintaining redox homeostasis with multiple components, targets, and links.

• 사상체질의학회지
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• 제1권1호
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• pp.87-112
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• 1989

In order to investigate experimentally the effects of Sung-yangikgibujat'ang (SIT) and Kwangyebujalijungt'ang (KBT) on Yang-insufficient syndrome (陽虛證) induced by Hydrocortisone acetate (H.A.) in experimental animals (Mice and Rat), the author experimented various activities. Delayed type hypersensitivity (DTH), Rosette forming cells (RFC), hemagglutinin (HA) titers, Hemolysin (HL) titers, Body weight, Whole blood viscosity, Plasma Viscosity, Hematocrit, RBC, Albumin, Total protein, Triglyceride, cholesterol and Glucose were measured. The results summerized as follows; 1. In DTH and RFC all the experimental groups were increased significantly in comparison to the H.A.-treated group. 2. In HA titers SIT_treated group were increased significantly and KBT-treated group showed increasing tendancy, but showed no significance. 3. In HL titers all the experimental groups showed increasing tendancy, but showed no significance. 4. In body weight all the experimental groups showed increasing tendancy, but showed no significance. 5. In whole blood viscosity all the experimental groups were decreased significantly in comparison to the H.A.-treated group. 5. In whole blood viscosity all the experimental groups were decreased significantly in comparison to the H.A.-treated group. 6. In plasma viscosity KBT-treated group were decreased significantly and SIT-treated group showed decreasing tendancy, but showed no significance. 7. In Hematocrit SIT-treated group were decreased significantly and KBT-treated group showed decreasing tendancy, but showed no significance. 8. In RBC, albumin and cholesterol all the experimental groups were decreased significantly in comparison to the H.A.-treated group. 9. In total protein and triglyceride KBT-treated group were decreased significantly and SIT-treated group showed decreasing tendancy, but showed no significance. 10. In Glucose SIT-treated group were decreased significantly and KBT-treated group showed decreasing tendancy, but showed no significance. From above findings, it has been demonstrated that Sungyangikgibujat'ang and Kwangyebujalijungt'ang seem to produce the effectiveness on the recovery from depression of the cell-mediated immune response, blood circulation and energy metabolic rate, induced by Hydrocortisone acetate, and in the humoral immune response Sungyangikgibujat'ang have the effectiveness on the recovery, and in cellular component of blood Sungyangikgibujat'ang was more effective than Kwangyebujalijungt' ang, and in plasma of blood Kwangyebujalijungt'ang was more effective than Sungyangikgibujat'ang. Therefore it is suggested that Sungyangikgibujat'ang and Kwangyebujalijungt'ang have the effectiveness on the recovery from Yang-insufficient syndrome more or less.

• 대한수의학회지
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• 제34권2호
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• pp.287-299
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• 1994

Plasma protein which has been known as one of nonspecific immunostimulators was added to feedstuff to examine its effect on the enhancement of cellular immune response in porcine immune system. A total of 40 piglets, 20 male and 20 female each, were fed for 30 days with or without plasma protein. The peripheral blood were collected and analyzed for the investigation of leukocyte subpopulations and their activities by using a panel of monoclonal antibodies specific to porcine leukocyte differentiation antigens and flow cytometry. The results obtained as follows. 1. Subpopulations expressing major histocompatibility complex(MHC) class I antigen were $96.2{\pm}3.1%$ and $86.6{\pm}3.8%$ in piglets fed with plasma protein and in piglets fed without plasma protein, respectively. 2. Proportion of leukocyte subpopulation expressing MHC class II antigens were significantly higher in the piglets fed with plasma protein than ones without plasma protein. The proportion was $27.6{\pm}3.6%$ and $16.6{\pm}2.2%$ in MHC class II DQ antigen, and $28.1{\pm}2.0%$ and $20.0{\pm}0.3%$ in MHC class II DR antigen, respectively. 3. A significant increase in the proportion of cells expressing poCD2 was not found in piglets fed plasma protein. 4. Proportion of subpopulation expressed porcine(Po) CD4 antigens which specific to helper T lymphocytes were not increased (18.3-19.1% vs. 25.6-28.8%), rather slightly decreased, in plasma protein-treated group. 5. The most important increase of proportion in plasma protein-treated group was the leukocyte subpopulation specific to $poCD8^+$ T cytotoxic/suppressor lymphocytes. The expression level was significantly higher up to 45.9-47.1% in plasma protein-treated group in comparing with 29.7-33.0% in non-plasma protein-treated group. 6. Lymphoblastogenetic responses using different concentrations of Con A mitogen and plasma protein has found that the responses of lymphocyte from piglets fed plasma protein was significantly activated (p<0.01). The activities measured by 3[H]-thymidine incorporation showed 3-6 times stronger in plasma protein-treated group than those in non-plasma protein-treated group. The study has concluded that plasma protein, which has known as a nonspecific immunostimulator, may have an immunoenhancing activities in porcine lymphoid system by increase the activated cell proportions and their blastogenetic properties which is critical to host immune responses.

• Advances in Traditional Medicine
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• 제5권3호
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• pp.216-230
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• 2005

Although the field of study in immune enhancing compounds is relatively new, natural products from plants represent a rich and promising source of novel molecules with immunomodulating properties, Microglial cells, the main immune effector cells of the brain, usually display a ramified morphology and low expression levels of immunologically relevant antigens such as MHC class I and class II. Since any compound which participates in activation of phagocytic cells contributes to the production of potentially toxic factors, the search for convenient in vitro test-systems and study of mechanisms of action of these agents are of great interest. Human blood polymorphonuclear (PMN) cells and primary microglial cells isolated from Sprague-Dawley rats were used as cellular screening tests for study of phagocytosis-stimulating action of immunomodulating agents. Numbers of phagocytic activity were evaluated by the phagocyte ingestion of yeast cells and NO-synthase activity, nitrite production, and nitroblue tetrazolium test were determined after phagocyte stimulation. It was possible to demonstrate that indexes of phagocytic activity can be used as quantitative indicators for measurement immunomodulating activity. As a positive control, Zymosan A-induced phagocytosis in both PMN cells and primary microglial cells was used. $IFN-{\gamma}$ (0.1 -1 U/ml) stimulated phagocytosis in PMN cells 1.2 times after 2 - 3 h incubation, although at higher concentrations (10 - 100 U/ml) it strongly inhibited phagocytosis. In a similar way, at higher concentrations, $IFN-{\gamma}$ (100 - 500 U/ml) suppressed phagocytosis in zymosan-A stimulated microglial cells. When Polypodium leucotomus, cambricum and vulgare extracts were tested alone, increased levels of phagocytosis were observed in PMN. In addition, microglial cells showed both increased phagocytosis and MHC class-II antigen expressions. Surprisingly, when PMN and microglia were treated with a combination of Polypodium and $IFN-{\gamma}$, phagocytosis was not inhibited. We did not find changes in NO-synthase activity and nitrite production in both microglia and PMN cells activated by different immunomodulating agents. These results indicate that primary microglial cell cultures as well as human PMN cells can provide reproducible quantitative results in screening phagocytic activity of different immunoactive compounds. Furthermore, both inhibitory or activation mechanisms might be studied using these in vitro experimental approaches.

• 한국식품영양과학회지
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• 제41권4호
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• pp.494-500
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• 2012

본 연구에서는 면역억제 동물모델에서 밀리타리스 동충하초 50% 에탄올 추출물의 면역력 증강 기능을 평가하였다. 이를 위하여 C57BL/6 마우스에 cyclophosphamide를 2회 복강주사 하여 면역력을 억제한 후, 밀리타리스 동충하초 추출물을 30, 100, 300 mg/kg 용량으로 12일간 경구투여 하였다. 마우스를 희생하여 몸무게 및 면역장기 무게, 비장세포의 증식, 비장세포의 cytokine 분비능, NK 세포 활성을 측정하였다. 그 결과, cyclophosphamide 투여에 의한 면역억제는 마우스의 몸무게와 간의 무게에 영향을 주지 않았으나 흉선의 무게는 감소시켰고 비장의 무게는 증가시켰다. 밀리타리스 동충하초 추출물 투여는 마우스의 몸무게 및 면역장기 무게에 영향을 주지 않았다. Cyclophosphamide 투여는 비장세포의 증식능을 감소시켰으며 밀리타리스 동충하초 추출물은 용량 의존적으로 비장세포 증식을 증가시켜 실험에 사용한 전 용량에서 비장세포의 유의적인 증식효과를 보였다. 비장세포의 cytokine 분비능을 측정한 결과, 밀리타리스 동충하초 추출물 투여는 IL-2, IL-12, IFN-${\gamma}$, TNF-${\alpha}$ 같은 Th1 cytokine의 분비를 대조군에 비해 유의적으로 증가시켰으나, IL-4와 IL-10 같은 Th2 cytokine의 분비에는 영향을 미치지 않았다. 또한 cyclophosphamide는 NK 세포의 활성을 정상군에 비하여 유의적으로 감소시켰으며, 밀리타리스 동충하초 추출물 투여는 cyclophosphamide에 의해 저하된 NK 세포 활성을 현저하게 증가시켰다. 이상의 결과를 종합해 볼 때, 밀리타리스 동충하초는 면역력이 억제된 상황에서 면역력을 증강시키며, 이러한 면역력 증강 효과는 체액성 면역보다 세포성 면역력 증강에 기인하는 것으로 보인다.

• Journal of Animal Science and Technology
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• 제49권2호
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• pp.225-238
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• 2007

급성기 반응중 육계병아리의 생산성과 면역반응에 미치는 사료중 크릴 밀 수준의 영향이 조사되었다. 갓 부화한 육계병아리(Ross) 수컷을 크릴 밀 0.0(기초), 0.5, 1.0 및 2.0% 함유한 실험사료로 3주간 실험사육하고 9, 11 및 13일령에 Salmonella typhymurium LPS를 복강내 주입하여 급성기 반응을 활성화하였다. 1. 급성기 반응은 유의하게(p<0.05) 일당증체와 사료섭취량을 감소시키고, 간장과 비장의 무게를 증가시키나 사료중 크릴 밀 수준에 의한 영향은 유의하지 않았다.2. 크릴 밀 사료급여는 TNF-α 활성을 급성기 반응과 회복중에도 기초사료에 비해 낮추었다(p<0.05). 급성기 반응은 TNF-α 활성을 대조에 비해서 기초사료 급여로 유의하게 증가시키나(p< 0.05), 크릴 밀 사료급여시는 유의하지 않았다. 3. 급성기 반응은 혈중 오보트렌스훼린 수준을 대조에 비해서 기초사료, 크릴 밀 1.0 및 2.0% 사료급여로 증가시키나 크릴 밀 0.5% 사료급여로 감소시켰다.4. 급성기 반응중 PBMC 및 비장세포의 증식도는 크릴 밀 0.5% 사료급여로 차이가 없었으나, 크릴 밀 1.0 및 2.0% 사료급여시에는 오히려 감소하였다(p<0.05). 대조인 정상병아리에서는 크릴 밀 수준에 따라 비장세포의 증식도가 점차 증가하였다. 본 연구 성적은 급성 기 반응중인 육계병아리에서 사료중 크릴 밀 첨가가 혈중 TNF-α 활성과 ovotransferrin 분비를 감소시키고 PBMC와 비장세포 증식도에 미치는 영향은, 사료중 크릴 밀이 육계 병아리의 선천 면역성과 세포성 면역성과 관계가 있다는 것을 나타내었다. (색인 단어:lipopolisaccharide(LPS), tumor necrosis factor-α (TNF-α), PBMC와 비장세포의 증식, 크릴 밀, 육계 병아리)

• 한국식품영양과학회지
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• 제35권6호
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• pp.683-689
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• 2006

본 연구는 게르마늄강화효모 (germanium: 3,210 ppm, 400 mg${\times}$3회/day)가 인체의 혈청지질 및 면역세포 변화에 미치는 효과를 평가를 목적으로 $50{\sim}75$세의 남녀 50명을 대상으로 임상실험을 실시하였으며, 게르마늄강화효모 복용 전후에 따른 혈청지질 수준의 변화 및 면역증진 기능평가에 중요한 역할을 하는 NK세포, B세포, T세포 및 항암기능 효과를 지니는 $TNF-{\alpha}$의 생성의 변화를 확인하였다. 대조군과 보충군 모두 보충 전, 4주, 8주 후의 헤모글로빈, 헤마토크릿, 적혈구 지표(red blood cell indices) 및 백혈구 수, 혈소판, 혈당, ALT, AST, ALP, BUN, Cr, TB, TP, Alb, A/G ratio, ${\gamma}-globulin(g/dL)$이 보충에 따른 유의적인 차이는 나타나지 않았다. 총 콜레스테롤, LDL 콜레스테롤 및 HDL 콜레스테롤은 보충 전, 후에 따른 유의적인 차이는 나타나지 않았다. 중성지방의 경우 대조군에서는 보충 전, 후에 따른 유의적인 차이는 나타나지 않았으나, 게르마늄강화효모 보충군에서는 보충 전에 비해 보충 8주 후에는 p<0.05 수준에서 유의적으로 감소하는 것으로 나타났다. B세포의 경우 대조군에서는 보충 전, 후에 따른 유의적인 차이는 나타나지 않았으나, 게르마늄강화효모 보충군에서는 보충 전에 비해 보충 8주 후에는 p<0.05 수준에서 유의적으로 증가하는 것으로 나타났다. $TNF-{\alpha}$의 경우 대조군에서는 보충 전, 후에 따른 유의적인 차이는 나타나지 않았으나, 게르마늄강화효모 보충군에서는 보충 전에 비해 보충 8주 후에는 p<0.05 수준에서 유의적으로 증가하는 것으로 나타났다. 이는 게르마늄강화효모가 인체의 면역증진에 각종 암, 성인병의 예방과 치료, 인체 면역력의 증진 등 건강증진을 위한 새로운 기능성 원료로의 활용이 기대되며, 이에 대한 지속적인 연구가 사료 된다.