• 대한한방내과학회지
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• 제29권1호
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• pp.258-264
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• 2008

Objectives : The aim of this study was to confirm the characteristics of oral malodor patients by evaluating the differences of salivary flow rate, secretory immunoglobulin A (sIgA) level in saliva between the patient and control groups, and the correlation with the tongue coating, volatile sulfur compound (VSC), salivary flow rate and sIgA level in saliva in the patients group. Methods : Forty-seven patients with oral malodor and twenty healthy volunteers were included in this study. Their tongue coating was assessed with the Winkel tongue coating index, and salivary flow rate, sIgA concentrations in saliva and the level of VSC in oral cavity were measured. Results : There were no significant differences of the salivary flow rate and the sIgA level in saliva between the patient and control groups, but there was a significant relationship between the accumulation of tongue coating and the level of VSC in oral cavity. Conclusions : Our results suggest that tongue coating is closely related to oral malodor, but further studies are needed to confirm the relationship between tongue coating and sIgA level in saliva.

• Restorative Dentistry and Endodontics
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• 제19권2호
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• pp.372-383
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• 1994

Saliva plays an important role in modulating the oral microbial ecology. And it is suggested to influence the initiation and progression of the dental caries. To evaluate the correlations between the salivary antimicrobial agents and the caries susceptibility, the 51 subjects were divided into 3 groups according to caries experience ; caries resistant group, medium caries susceptible group, and high caries susceptible group. Stimulated whole saliva was collected, and the salivary levels were measured for lysozyme, lactoferrin, and secretory-IgA to Streptococcus mutans. The lysozyme level was estimated using Micrococcus diffusion plate, lactoferrin level was determined with a non-competitive avidin-biotin enzyme immunoassay, and the titer of secretory IgA to Streptococcus mutans was assayed with ELISA. The results were as follows: 1. Lysozyme levels of each group showed no significant difference statistically (p>0.05). 2. The caries resistant group and the medium caries susceptible group had significantly higher levels of lactoferrin than the high caries susceptible group (p<0.05). But no clear difference was observed between the caries resistant group and the medium caries susceptible group(p>0.05). 3. The caries resistant group and the medium caries susceptible group showed relatively higher levels of the secretory IgA to Streptococcus mutans than the pigh caries susceptible group, but no significant difference was observed statistically (p>0.05).

• Parasites, Hosts and Diseases
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• 제35권1호
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• pp.39-46
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• 1997

이 연구에서는 살아있는 질편모충의 단백질녈해효소가 인체 면역글로불린을 분해하는지 알아보고 질편모충에 의한 조직세포 독성에 있어서 단백질분해효소의 역할을 시험관내에서 관찰하였다 실험에 사용한 질편모충은 질염환자로년터 분리한 KT9 분리주이었으며 세포독성을 알아보기 위한 표적세포로는 HeLa 세포를 사용하였다 질편모충 단백질분해효소가 인체 면역글로불린을 분해하는지 관찰하고자 인체의 분비 IP. 혈청 IgA 및 IgG를 살아있는 원충. 원충의 용출액 및 분비-배설 액과 DTT를 넣어 반응시켰다. 여러 계열의 단백질분해효소 저해제(aminopeptidase, serine, metallo, cystelrle계열)를 살아있는 질편모충과 미리 반응시킨 후 세척하고 면역글로불린의 분해 단백질분해효소 활성 및 조직세포독성에 미치는 영향을 관찰하였다 살아있는 질편모충은 인체의 분비 IgA. 혈청 IgA 및 IgG를 분해하였는데 질편모충 수가 증가할수록 반응시간이 길수록 분해가 더 잘 이루어졌다 질푄모충의 용출액과 분비-배설액도 분비 IgA. 혈청 IgA 및 IgG를 분해하였다. Cysteine, serine계 열의 단백질분해효소 저해제 (I-64 antipain, iodoacetic acid, iodoacetamide, TLCK)를 처리한 질편닐충은 분비 IgA의 분해를 저해하였으며. 단백질분해효소저해제로 처리한 경우 질편모충의 단백질븐해효소 활성은 감소하였고 HeLa세포에 대한 독성이 감소하였다. 이상의 성적을 종합하면 질편모충에서 분비되는 단백질분해효소는 시험관내에서 조직세포에 세포독성을 나타내며 또한 인체면역글로불린을 분해하여 숙주의 방어기전에 대한 도피물질로 작용하는 것으로 생각된다.

• 한국치위생학회지
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• 제16권3호
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• pp.463-469
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• 2016

Objectives: The purpose of the study is to investigate the effect of chewing gum containing Prunus mume extract(PME) on the change of saliva ingredients. On the basis of the biological background of molecules and diagnostic indices in the use of saliva, the mastication effect of chewing gum containing PME was demonstrated in terms of secretory IgA concentration and total protein concentration in stimulated saliva. Methods: This study is an experimental research on the use of a research design before and after applying a randomized control group. Participants were distributed randomly to the experimental group and the control group, respectively. The experiment group was instructed to masticate the chewing gum containing PME for 10 minutes for one month after each meal within 30 minutes. Salivary secretion was collected by the participants between 8 and 10 a.m in the morning in the research office. For the measurement of secretory IgA and total protein concentrations in the saliva, indirect enzyme-linked immunosorbent assay(ELISA) was used. Results: The salivation stimulation rate was significantly increased after four weeks of masticating chewing gum containing PME after each meal(p<0.001). Mastication of chewing gum containing PME for four weeks decreased the concentration of secretory IgA much more significantly than that after mastication for one week(p=0.003). The concentration of total protein in the saliva was decreased after four weeks in the experimental and control groups. Conclusions: Mastication of chewing gum containing PME stimulated salivary secretion and led to oral disease prevention in patients with xerostomia. Furthermore, it seems to be urgent to seek measures that can be utilized in intervention for patients with xerostomia.

• Parasites, Hosts and Diseases
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• 제40권2호
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• pp.93-99
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• 2002

The effect of a secretory proteinase from the pathogenic amoebae Acanthamoeba castellanii on host's defense-oriented or regulatory proteins such as immunoglobulins, interleukin-1, and protease inhibitors was investigated. The enzyme was found to degrade secretory immunoglobulin A (slgA), IgG, and IgM. It also degraded $interleukin-1{\alpha}$ ($IL-l{\alpha}$) and $IL-l{\beta}$. Its activity was not inhibited by endogenous protease inhibitors, such as ${\alpha}$2-macroglobulin, ${\alpha}l-trypsin$ inhibitor, and ${\alpha}2-antiplasmin$. Furthermore, the enzyme rapidly degraded those endogenous protease inhibitors as well. The degradation of host's defense-oriented or regulatory proteins by the Acanthanoeba proteinase suggested that the enzyme might be an important virulence factor in the pathogenesis of Acanthamoeba infection.

• Biomolecules & Therapeutics
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• 제11권3호
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• pp.157-162
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• 2003

The generation of secretory IgA antibodies(Abs) for specific immune protection of mucosal surfaces depends on stimulation of the mucosal immune system, but this is not effectively achieved by parenteral or even oral administration of most soluble antigens. Thus, to produce a possible vaccine antigen against urinary tract infections, the uropathogenic E. coli (UPEC) adhesin was genetically coupled to the ctxa2b gene and cloned into a pMAL-p2E expression vector. The chimeric construction of pMALfimHIctxa2b was then transformed into E. coli K-12 TB1 and its nucleotide sequence was verified. The chimeric protein was then purified by applying the affinity chromatography. The purified chimeric protein was confirmed by SDS-PAGE and western blotting using antibodies to the maltose binding protein (MBP) or the cholera toxin subunit B (CTXB), plus the N-terminal amino acid sequence was analyzed. The orderly-assembled chimeric protein was confirmed by a modified $G_{M1}$-ganglioside ELISA using antibodies to adhesin. The results indicate that the purified chimeric protein was an Adhesin/CTXA2B protein containing UPEC adhesin and the $G_{M1}$-ganglioside binding activity of CTXB. This study also demonstrate that peroral administration of this chimeric immunogen in mice elicited high level of secretory IgA and serum IgG Abs to the UPEC adhesin. The results suggest that the genetically linked CTXA2B acts as a useful mucosal adjuvant, and that the adhesin/CTXA2B chimeric protein might be a potential antigen for oral immunization against UPEC.

• 농업과학연구
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• 제22권1호
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• pp.82-95
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• 1995

본(本) 연구(硏究)는 한국인(韓國人) 산모(産母)로 부터 수집한 초유(初乳) 및 Holstein종(種)으로 부터 수집한 초유(初乳) 중에 존재하는 Secretory immunoglobulin A의 분리방법(分離方法)을 검토하고 분리(分離)된 분획들의 면역화학적(免疫化學的) 특성을 비교 검토하여 향후 인공영양(人工營養)에 대한 시험(試驗) 자료를 얻고자 하였으며 그 결과(結果)는 다음과 같다. 1. 인유(人乳) 초유(初乳) 중의 SIgA는 Sephadex G-200과 Sepharose 6B를 통한 gel-filtration 만으로도 순수한 상태로 분리(分離) 정제할 수 있었으나, 우유(牛乳) 초유(初乳) 중의 SIgA는 gel-filtration을 반복하는 방법(方法)으로는 순수한 상태로 분리(分離) 및 정제할 수 없었으며, gel-filtration으로 얻어진 SIgA rich fraction을 모아서 DEAE를 실시한 결과(結果) 또한 마찬가지로 SIgA를 순수한 상태로 분리(分離)할 수는 없었다. 2. 인유(人乳) 초유(初乳)로 부터 gel-filtration을 통하여 분리(分離)한 분획들을 Immunoelectrophoresis 및 Double immunodiffusion 방법(方法)으로 면역화학적(免疫化學的) 특성을 살펴본 결과(結果), 첫번째 peak의 분획에서 IgM이 존재하고 있음을 확인할수 있었으며 두번째 peak의 분획에서 SIgA가 순수한 상태로 존재하고 있음을 확인할수 있었다. 반면에 우유(牛乳) 초유(初乳)로 부터 gel filtration 및 DEAE를 통하여 분리(分離)한 분획들을 같은 방법(方法)으로 면역화학적(免疫化學的) 특성을 살펴본 결과(結果), SIgA rich fraction 중에는 IgG가 다량(多量)으로 혼재(混在)되어 있음을 확인할 수 있었다. 3. 우유(牛乳) 초유(初乳)에서 분리(分離)한 SIgA rich fraction의 Fragment를 SDS-PAGE로 분자량을 측정해 본 결과(結果), Secretory component가 77,000-80,000, Heavy chain이 50,000-60,000, Light chain이 25,000-27,000 dalton으로 나타났으며 J-chain은 Light chain과 중복되어 분자량 측정이 어려웠다. 이와같은 결과(結果)는 인유(人乳) 초유(初乳) 중에 존재하는 SIgA Fragment 분자량과 유사한 결과(結果)를 보여주었다.

• Parasites, Hosts and Diseases
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• 제32권4호
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• pp.249-258
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• 1994

톡소포자충(Tomplasmngondii)은 세포내에 기생하는 구포자충(Cuidia)의 일종으로 항원은 여러 가지 단백질로 구성되어 있으며 이들 항원의 분석은 면역학적 생화학적인 면에서 시도 해 볼 필요가 있다. 톡소포자충(RH주) tachyzoite의 용해물 및 분비항원을 SDS-PAGE(sodium dodecyl sulfate polyacrylamide gel electrophoresis)로 단백질 분획을 관찰하고 면역 전기영동이적법 (EITB, enzyme-linked immunelectrohansfer blot)을 시행하여 반응대를 관찰하였다. 토끼 (New Zealand산) 또는 BALB/c마우스를 톡소포자충으로 면역 또는 감염시키고 3주 또는 7주 후에 채혈 하였다. 면역 후 토끼나 마우스 혈청은 간접형광항체법(IFA)으로 항체가 1:1024 또는 1 : 128임을 확인하였다. 톡소포자충 용해물 및 분비항원으로 SDS-PAGE를 시행하였을 때 10 kDa에서 220 kDa까지 광범위한 단백질 분포대를 보였다. 톡소포자충 용해물 항원을 IgG 항혈청과 반응시켰을 때 주요 항원의 분자량은 23에서 35 kDa까지 5개의 반응대를 관찰하였으며 IgG와 IgM의 공동반응 대는 24. 27, 30. 35 kDa에서 관찰되었다. 분비항원을 IgG 항혈청과 반응시켰을 때 감염 마우스 의 복강액을 항원으로 한 경우 33(P30), 45 kDa의 반응대가 주요 항원임을 알 수 있었고 톡소포자 충을 CHL 세포로 in vitro에서 배양시킨 후 배양액의 상청액을 항원으로 EITB를 시행하였을 때 20 kDa. 30 kDa 이하의 분획에서 반응대가 관찰되었다. 이상으로 30 kDa 항원이 톡소포자충 tachyzoite의 용해물 뿐만 아니라 분비물에서도 관찰되는 중요한 항원임을 알 수 있었다.

• Parasites, Hosts and Diseases
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• 제52권4호
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• pp.367-376
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• 2014

Recombinant antigenic proteins of Toxoplasma gondii are alternative source of antigens which are easily obtainable for serodiagnosis of toxoplasmosis. In this study, highly antigenic secretory organellar proteins, dense granular GRA2 and GRA3, rhoptrial ROP2, and micronemal MIC2, were analyzed by bioinformatics approach to express as water-soluble forms of antigenic domains. The transmembrane region and disorder tendency of 4 secretory proteins were predicted to clone the genes into pGEX-4T-1 vector. Recombinant plasmids were transformed into BL21 (DE3) pLysS E. coli, and GST fusion proteins were expressed with IPTG. As a result, GST fusion proteins with $GRA2_{25-105}$, $GRA3_{39-138}$, $ROP2_{324-561}$, and $MIC2_{1-284}$ domains had respectively higher value of IgG avidity. The $rGST-GRA2_{25-105}$ and $rGST-GRA3_{39-138}$ were soluble, while $rGST-ROP2_{324-561}$ and $rGST-MIC2_{1-284}$ were not. $GRA2_{31-71}$, intrinsically unstructured domain (IUD) of GRA2, was used as a linker to enhance the solubility. The $rGST-GRA2_{31-71}-ROP2_{324-561}$, a chimeric protein, appeared to be soluble. Moreover, $rGST-GRA2_{31-71}-MIC2_{1-284}$ was also soluble and had higher IgG avidity comparing to $rGST-MIC2_{1-284}$. These 4 highly expressed and water-soluble recombinant antigenic proteins may be promising candidates to improve the serodiagnosis of toxoplasmosis in addition to the major surface antigen of SAG1.

• 한국임상수의학회지
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• 제20권1호
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• pp.59-65
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• 2003

This study was performed to investigate the immunopotentiative effects of conjugated linoleic acid on mice immunosuppressed by administratin corticoids. Mice were divided into four groups of 8 mice. Two groups (C, CP) were given diet supplemented with 1% linoleic acid (CLA) and the other two groups (L, LP) were given diet supplemented with 1% linoleic acid (LA) instead of CLA. Prednison was administered to two groups (CP, LP) for immune depression. After feeding diets for 3 weeks containing PDS injection for last 1 week. Serum and gut lumen lavage were taken. Measurement of total Ig were executed using sandwich ELISA. Serum levels of IgA, IgG, and IgM showed some trend which groups fed with CLA were higher than groups fed with LA while IgE was reduced in those fed the CLA intake, and groups administered with PDS were lower than groups administered with saline. However, no significant differences were seen in the proportion of total immunoglobulin in serum. In case of secretory IgA, Group C and CP were significantly higher than group L and LP. Especially between CP and LP, it can be seen effects of CLA. In addition that the CLA treated group weighted a significantly lower level than the one's that have not been treated with CLA. These result support the view that CLA potentiate the immune response and prevent immune depression caused by administrating of corticoids. In conclusion, CLA produced a situation favorable for immunopotentiative effects. Thus, the clinical application of CLA is warranted.