• IMMUNE NETWORK
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• 제15권1호
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• pp.37-43
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• 2015

It is well established that TGF-${\beta}1$ and retinoic acid (RA) cause IgA isotype switching in mice. We recently found that lactoferrin (LF) also has an activity of IgA isotype switching in spleen B cells. The present study explored the effect of LF on the Ig production by mouse peritoneal B cells. LF, like TGF-${\beta}1$, substantially increased IgA production in peritoneal B1 cells but little in peritoneal B2 cells. In contrast, LF increased IgG2b production in peritoneal B2 cells much more strongly than in peritoneal B1 cells. LF in combination with RA further enhanced the IgA production and, interestingly, this enhancement was restricted to IgA isotype and B1 cells. Similarly, the combination of the two molecules also led to expression of gut homing molecules ${\alpha}4{\beta}7$ and CCR9 on peritoneal B1 cells, but not on peritoneal B2 cells. Thus, these results indicate that LF and RA can contribute to gut IgA response through stimulating IgA isotype switching and expression of gut-homing molecules in peritoneal B1 cells.

• IMMUNE NETWORK
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• 제4권4호
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• pp.216-223
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• 2004

Background: It is well known that IgA isotype switching is induced by $TGF-{\beta}1$. LPS-activated mouse normal B cells well differentiate into IgA secreting plasma cells under the influence of $TGF-{\beta}1$. Nevertheless, there are lots of difficulties in studying normal B cells in detail because it is not simple to obtain highly purified B cells, showing low reproducibility and transfection efficacy, moreover impossible to keep continuous culture. To overcome these obstacles, it is desperately needed to develop B cell line which acts like normal B cells. In the present study, we investigated whether CH12F3-2A lymphoma cells are appropriate for studying IgA isotype switching event. Methods: CH12F3-2A B cell line was treated with LPS and $TGF-{\beta}1$, then levels of germ-line (GL) transcripts were measured by RT-PCR, and $GL{\alpha}$ promoter activity was measured by luciferase assay. In addition, membrane IgA (mIgA) expression and IgA secretion were determined by FACS and ELISA, respectively. Results: $TGF-{\beta}1$, regardless of the presence of LPS, increased level of $GL{\alpha}$ transcripts but not $GL{\gamma}2b$ transcripts. However, IgA secretion was increased dramatically by co-stimulation of LPS and $TGF-{\beta}1$. Both mIgA and IgA secretion in the presence of $TGF-{\beta}1$ were further increased by over-expression of Smad3/4. Finally, $GL{\alpha}$ promoter activity was increased by $TGF-{\beta}1$. Conclusion: CH12F3-2A cell line acts quite similarly to the normal B cells which have been previously reported regarding IgA expression. Thus, CH12F3-2A lymphoma cell line appears to be adequate for the investigation of the mechanism(s) of IgA isotype switching at the cellular and molecular levels.

• 한국가금학회지
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• 제31권1호
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• pp.37-44
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• 2004

It has been recognized that the hen, like its mammalian counterparts, provides young chicks with antibodies as protection against hostile invaders. This system facilitates the transfer of specific antibodies from serum to egg yolk, and provides a supply of antibodies called immunoglobulin Y(IgY) to the developing embryo and the hatched chick. The protection against pathogens that the relatively immune-incompetent newly hatched chick has, is through transmission of antibodies from the mother via the egg. Egg yolk, therefore, can be loaded with a large amount of IgY against pathogens which can immobilize the existing or invading pathogens during the embryo development or in day-old chicks. Thus, the immunization of laying hens to various pathogens results in production of different antigen-specific IgY in eggs. Egg yolk contains 8∼20 mg of jmmunoglobulins (IgY) per ml or 136∼340 mg per yolk suggesting that more than 30 g of IgY can be obtained from one immunized hen in a year. By immunizing laying hens with antigens and collecting IgY from egg yolk, low cost antibodies at less than $10 per g compared to more than $20,000 per g of mammalian IgG can be obtained. This IgY technology opens new potential market applications in medicine, public health, veterinary medicine and food safety. A broader use of IgY technology could be applied as biological or diagnostic tool, nutraceutical or functional food development, oral-supplementation for prophylaxis, and as pathogen-specific antimicrobial agents for infectious disease control. This paper has emphasized that when IgY-loaded chicken eggs are produced and consumed, the specific antibody binds, immobilizes and consequently reduces or inhibits the growth or colony forming abilities of microbial pathogens. This concept could serve as an alternative agent to replace the use of antibiotics, since today, more and more antibiotics are less effective in the treatment of infections, due to the emergence of drug-resistant bacteria.

• Tuberculosis and Respiratory Diseases
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• 제77권2호
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• pp.85-89
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• 2014

Intrathoracic involvement of immunoglobulin G4 (IgG4)-related disease has recently been reported. However, a subset of the disease presenting as interstitial lung disease is rare. Here, we report a case of a 35-year-old man with IgG4-related lung disease with manifestations similar to those of interstitial lung disease. Chest computed tomography showed diffuse ground glass opacities and rapidly progressive pleural and subpleural fibrosis in both upper lobes. Histological findings showed diffuse interstitial lymphoplasmacytic infiltration with an increased number of IgG4-positive plasma cells. Serum levels of IgG and IgG4 were also increased. The patient was diagnosed with IgG4-related lung disease, treated with anti-inflammatory agents, and showed improvement. Lung involvement of IgG4-related disease can present as interstitial lung disease and, therefore, should be differentiated when evaluating interstitial lung disease.

• Restorative Dentistry and Endodontics
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• 제9권1호
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• pp.37-49
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• 1983

This study was undertaken to observe the relationship between salivary IgA, IgG, agglutinin titer & dental caries. The subjects divided into two groups, an active caries group (AC group) and caries-free and treated caries group (CFTC group). The AC group consisted of 36 subjects who had one or more carious lesions and the CFTC group of 12 subjects who had no evidence of caries or had filled teeth without present carious teeth for the last six months. The IgA, IgG and IgM levels in their saliva were measured by single radial immunodiffusion method using a disposable low-level immunodiffusion plate. The salivary agglutinin titers to Streptococcus mutans were measured by microtitration system. The results were as follow; 1. The mean value of IgA concentration in saliva of AC group was slightly higher than that of CFTC group, but its difference was slight. 2. The mean value of IgG concentration in saliva of AC group was slightly lower than that of CFTC group. The IgM concentration in saliva of both groups was neither below 1.1 mg/dl nor detected on LC partigen immunodiffusion plate. 3. There was no difference in the agglutinin titer to S. mutans antigen by serotypes, but low level agglutinin to type d was measured in both groups. 4. AC group showed low correlation between IgA, IgG & DMFT, but CFTC group revealed negative correlation. 5. The relationship between salivary IgA & agglutinin titers to S. mutans was low correlation in AC group, but CFTC group showed significant positive correlation. (P<0.05) 6. There were no specific correlations among the concentrations of salivary immunoglobulins, agglutinin titers to S. mutans, and the DMF teeth. They had no close concern to induce the dental caries.

• Journal of Nutrition and Health
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• 제29권6호
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• pp.569-577
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• 1996

This study was performed to determine the effect of maternal protein intake on 1) the concentration of immune substances in milk 2) degree of passive immunity to pups via lactation, and 3) specific antibody production to a specific antigen, $\beta$-lactoglobulin(BLG). 4) the effect of passive immunity that pups received from mother during lactation on the production of antibodies when the pups were challenged to the same antigen. Part of the female rats were immunized with BLG before and during pregnancy. The pregnant rats were placed into either 25% or 10% isolated soy protein diet throughout gestation and lactation. After weaning, pups from each group continued to be fed the same diet. At 18 weeks of age, all the pups were challenged with BLG. Total IgA and IgG, lysozyme, BLG-specific IgA and IgG were measured in dam's serum, dam's milk, and pup's serum. Total IgG, and lysozyme in dam's serum and milk were higher in high protein group. Total IgA and IgG in pup's serum remained higher in high protein group from 5 to 18 weeks of age. BLG-specific antibodies were found in the milk and serum of immunized dams, and in serum of pups born to immunized dams but not in the non-immunized group. BLG-specific IgA and IgG were again higher in high protein group and declined with time. The concentration decreased faster in the low proetein group than in the high protein groups. After immunization the pups with LBG, serum BLG-specific antibodies were not differ between rats born to immunized dams and those born to non-immunized dams. Therefore passive immunity rats received via milk as a pup had no effect on the BLG-specific antibody production later in life. This study shows the importance of protein status of mother and strongly support to the endorsement of breast feeding.

• Parasites, Hosts and Diseases
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• 제45권3호
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• pp.175-180
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• 2007

In order to determine the role of Peyer's patch lymphocytes (PPL) in self-clearing of Cryptosporidium parvum infection in murine models, changes in PPL subsets, their cytokine expression, and in vitro IgG1 and IgA secretions by PPL were observed in primary- and challenge-infected C57BL/6 mice. In primary-infected mice, the percentages of CD4+ T cells, CD8+ T cells, slgA+ B cells, IL-2+ T cells, and $IFN-{\gamma}+$ T cells among the PPL, increased significantly (P < 0.05) on day 10 post-infection (PI). Secretion of IgG1 and IgA in vitro by PPL also increased on day 10 PI. However, all these responses, with the exception of IgG1 and IgA secretions, decreased in challenge-infected mice on day 7 post-challenge (= day 13 PI); their IgG1 and IgA levels were higher (P > 0.05) than those in primary-infected mice. The results suggest that murine PPL play an important role in self-clearing of primary C. parvum infections through proliferation of CD4+, CD8+, IL-2+, and $IFN-{\gamma}+$ T cells, and IgG1 and IgA-secreting 8 cells. In challenge infections, the role of T cells is reduced whereas that of 8 cells secreting IgA appeared to be continuously important.

• Parasites, Hosts and Diseases
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• 제26권1호
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• pp.15-26
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• 1988

뇌 유구낭미충증의 진단에는 혈청뿐만 아니라 뇌척수액내 특이 IgG항체가도 측정하여 혈청학적 진단의 민감도를 약 10% 높일 수 있다. 이 경우 뇌척수액내 특이 IgG항체가 그 환자의 혈청에서 혈관-뇌 장벽을 넘어 이전된 것인지 또는 두개강내 병변에 형성된 육아종에서 생성한 것인지를 결정하는 일은 뇌척수액내 특이 IgG항체가 측정의 의미를 부여하는 데에 중요하다. 이 연구는 그 기원을 찾기 위하여 실시하였다. 확진된 뇌 유구낭미충증 환자 82례와 기타 신경계질환 환자 및 건강대조인 45례에서 오은 혈청과 뇌척수액에서 각각 총단백질, 알부민 및 IgG 농도를 측정하였다. 그리고 Tourtellotte and Ma (1978)의 공식에 의하여 뇌척수액내 IgG농도를 여출(濾出, transudation; 혈관-뇌장벽이 정상인 상태에서 생리적으로 뇌척수액으로 이전된 것), 삼출(渗出, exudation; 혈관-뇌장벽이 파괴된 상태에서 병적으로 이전된 것) 및 두개강내 생사 등 세가지 기원으로 분리하였다. 고리고 혈청 및 뇌척수액내 특이 IgG항체가를 효소 면역측정법으로 측정하였다. 뇌척수액내 특이 Ig9G항체가와 각기원별 IgG량과의 관계를 통계학적으로 검정하였다. 그 결과를 요약하며 다음과 같다. 1. 뇌 유구낭미충증 환자 뇌척수액에는 총단백질, 알부민 및 IgG평균치가 상승되어 있었다. 각 단백질 농도는 혈청내 특이 IgG항체가와는 관계없이 뇌척수액내 IgG항체가 양성자에서 높았다. 2. 뇌 유구낭미충증 환자의 뇌척수액내 IgG량(14.0mg/dl)은 여출(4.52mg/dl), 삼출(2.94mg/dl) 및 두개강내 생산(6.88mg/dl)으로 구성되었다. 뇌척수액왜 특이 IgG항체가는 여출 및 삼출에 의한 IgG양과는 통계학적 유의성이 없는 관계이었으나 두개강내 생산량과는 유의한 관계가 있었다. 3. 제 4뇌실에 병 변이 화인된 뇌유구낭미충증 환자의 측뇌실에서 얻은 뇌척수액에는 총단백 질, 알부민 및 IgG량이 정상범위이었고 특이 IgG항체는 음성이 었다. 같은 환자의 요추천자로 얻은 뇌척수액에서는 각 단백질이 상승되어 있었고 특이 IgG항체가는 양성이었다. 4. 뇌 유구낭미충증 환자의 뇌척수액내 EgG량중 삼출에 의한 양이 증가된 예에서는 대부분 두개강내 IgG생산이 동반되고 있었다. 따라서 삼출에 의한 뇌척수액내 IgG 출현은 뇌유구낭미충증의 진행중 어느 시기에 특히 심한 것으로 추정된다. 이상의 결과에서 유구낭미충증 환자의 뇌척수액내 특이 IgG항체는 두개 강네 병변에서 생산된 것임을 알 수 있었다. 따라서 뇌척수액을 이용한 특이 IgG항체 측정은 진단에 도움이 된다고 생각된다.

• Asian Pacific Journal of Cancer Prevention
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• 제17권1호
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• pp.281-283
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• 2016

The Cholangiocarcinoma is a. The risk of development of cholangiocarcinoma, generally a rare type of a liver tumor, increases during infection of Opisthorchiasis. For this reason the timely detection of Opisthorchiasis is important for Cholangiocarcinoma prevention. There are many studies which concern the detection of pathogenesis of Opisthorchis viverrini infection but a little known about Opisthorchis felineus. In this study we investigate a correlation of the eggs which are found in a faeces and are comparable with a serum Ig G and Ig M antibody level that were detected with ELISA test in a large group of patients. The result is showing positive correlation between evidence of the Opisthorchis felineus eggs that were found in a faeces and antibody Ig G and Ig M level in a serum. Moreover the combination of two methods can improve the Opisthorchiasis diagnostic: the serum antibody and faeces investigation of eggs.

• Parasites, Hosts and Diseases
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• 제28권1호
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• pp.25-30
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• 1990

질트리코모나스(Trichomonas vaginalis)감염 환자 30명과 비감염 건강 대조군 30명을 패 상으로 혈청 내 항-질트리코모나스 IgG 및 IgM 항체가를 효소표식 면역검사법(enzyme-linked immunosorbent assay: ELISA)으로 측정하여 이 질환 진단법으로서 ELISA의 이용 가능성을 검토 하고, 현펑 내 IgG 및 IsM 항체가의 상관성을 알아보았다. 질트리코모나스 환자의 혈청 내 IgG 항체가는 0.37±0.134로 건강 대조군의 0.21±0.054 보다 유 의하게 높았다(p<0.005). 또 혈청 내 IgG 항체가 0.32 이상을 양성으로 하였을 때 ELISA 진단법 의 감수성은 70.0%이었고 특이성은 96.7%이었다. 질트리코모나스 환자의 혈청 내 IsM 항체가는 0.33±0.177로 건강 대조군의 0.11±0.051 보다 유의하게 높았다(p<0.005). 또 혈청 내 Is변 항체 가 0.21 이상을 양성 반응으로 하였을 때 감수성은 70.0%이었고 특이성은 96.7%이었다. 질트리코 모나스 환자의 혈청 내 IgG 와 IsM 항체가의 상관 관계는 상관계수 r=0.77로 유의한 상관관계가 인 정 되 었 다(p<0.005). 이상의 결과로 보아 질트리코모나스 환자에서 혈청 내 19G 및 IsM 항체가를 ELISA법으로 측정 함으로써 질트리코모나스 감염을 진단하거나 역학적 조사에 이용할 수 있을 것으로 생각된다.