• Parasites, Hosts and Diseases
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• 제21권2호
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• pp.270-280
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• 1983

임상적으로 폐흡충증이 의심되나 충란검출이 안되었던 155예(3예는 충란발견)의 피내반응 양성례에 대하여 Agar-gel Diffusion (AGD)반응, Counterimmunoelectro-phoresis(CIEP)반응 및 Enzyme-Linked Immunosorbent Assay(ELISA)를 실시하여 이들사이의 상관관계를 검토하였다. AGD 반응과 CIEP 반응은 폐흡충친항원원액(단백농도 7.56mg1m1)과 혈청원연을 사용하였고 ELISA반응에서는 상기 조항원의 40,000배 희석항원을, 그리고 혈청은 100배 및 200배 희석혈청을 사용하였다. 1. AGD 반응과 CIEP 사이의 양성반응의 일치률은 98%이었고 융성반응의 일치률은 100%이었다. 침강대는 AGD 반응에서 1∼3개가 흔히 관찰되었고 CIEP 반응에서는 1∼7개가 관찰되었으며 염색강도도 후자에서 일부의 피검혈청에서 강하게 나타났다. 2. AGD 반응과 ELISA 반응은 사성반응에서는 100배 희석혈청에서 96%, 그리고 200배 희석혈청에서 94%의 일치률을 나타내었고, 음성반응에서는 100석 희석혈청 및 200배 회석혈청에서 각각 97%와 99%의 일치율을 나타내었다. 3. CIEP와 ELISA 반응은 양성반응에서 100배 희석혈청에서는 98%, 200배 희석혈청에서는 96%의 일치률을 나타내었고 융성반응에서는 100배 희석혈청에서 97%, 200배 희석혈청에서 99%의 일치률을 나타내었다. 4. 대조혈청인 간흡충감염 혈청, 아메바감염 혈청 및 Toxoplaima형광항체반응 양성혈청에 대한 AGD 반응, CIEP 및 ELISA 반응은 전례에서 음성이었다. 이상의 결과로 볼 때 반응에 사용된 항원-항혈청의 농도로 보아서는 ELISA 반응의 감수성이 월등히 높았다. 같은 농도의 항원과 혈청을 사용한 AGD와 CIEP 반응에서는 CIEP에서 침강반응의 염색강도가 보다 강하게 나타난 것으로 보아 세가지 반응의 감수성의 높은 순위는 ELISA, CIEP, AGD라고 보여진다. 그러나 본 실험에서 AGD와 CIEP반응에서 ELISA보다 높은 농도의 항원과 항혈청을 사용하였을 때 감수성의 차이는 거의 볼 수 없는 유사한 상관관계의 반응을 나타내었다. 즉 반응방법에 따라 적절한 농도의 항원과 항혈청을 사용한다면 감수성의 차이는 없다고 본다. 세가지 반응의 유효성 으로 볼 때 가장 수기가 간편한 AGD 반응은 조항원을 사용할 때 용이하게 사용할 수 있는 방법이라 생각되며 CIEP는 AGD보다 전기영동장치가 필요한 번거로움이 있으나 보다 조기에 반응 결과를 알 수 있다. 가장 감수성이 예민한 ELISA반응은 항원을 정제하여 소동의 항원으로 다수의 집권집사를 할 수 있는 가장 바람직한 방법이라 생각된다. (본 실험을 수행함에 있어 ELISA 반응을 검사해 주신 연세의대 기생충학교실의 장재경 선생님께 감사드립니다)

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제4권1호
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• pp.34-40
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• 2001

목 적: 로타바이러스에 의한 장염의 진단에서 RT-PCR을 ELISA나 LA와 비교하여 각 검사의 효율을 비교하였다. 방 법: 설사증을 주소로 내원한 유소아의 대변에서 ELISA나 LA에 의한 로타바이러스 항원 검출률과 RT-PCR에 의한 로타바이러스 유전자 검출률을 비교하였다. 결 과: 대변에서 로타바이러스 감염을 진단하는데 있어 ELISA는 LA보다 우월하며 RT-PCR과 특이도의 의미있는 차이없이 상당한 일치를 보였다. 결 론: 로타바이러스 장염의 진단에서 ELISA는 LA보다 우월하며 RT-PCR은 ELISA 보다 의미있게 우월하지는 않았다.

• Parasites, Hosts and Diseases
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• 제47권2호
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• pp.153-157
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• 2009

Diagnosis of hydatidosis is based on immunodiagnostic methods along with radiological and ultrasound examinations. The objectives of the present study were to develop a specific and simple antigen-based ELISA method for diagnosis of hydatidosis and compare it with antibody detection method. The subjects in this study included 89 patients in the following groups: surgically confirmed hydatidosis patients (35 cases), control with other parasitic diseases (29 cases), and healthy controls (25 cases). Hyperimmune serum was raised against hydatid cyst fluid in rabbits. Anti-hydatid cyst IgG was purified by affinity chromatography using protein A column and labeled with horseradish peroxidase. Collected sera were assessed for hydatid cyst antigens and antibody by ELISA. Circulating hydatid antigen was found in 9 out of 35 patients with surgically confirmed hydatidosis. A sensitivity of 25.7% and a specificity of 98.0% were calculated for the antigen detection assay. Antibody detection by indirect ELISA, using antigen B, showed that 94.2% of patients (33 cases) have anti-hydatid cyst antibodies in their serum while cross reaction was noted in a few of non-hydatidosis patients. A sensitivity of 94.2% and specificity of 81.6% were found for the antibody detection assay. Findings of this study indicated that antibody detection assay is a sensitive approach for diagnosis of hydatid cyst while antigen detection assay might be a useful approach for assessment of the efficacy of treatment especially after removal of the cyst.

• 약학회지
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• 제45권2호
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• pp.180-189
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• 2001

We have reported that water-extracted Korean mistletoe (KM-110) had various biological activities such as antitumor and immunomodulatory activity, and the pectin fraction (KML-C) of the extract was one of major factors related to its biological functions. In this paper, we produced murine monoclonal antibody (mAb) against KML-C. The cAbs obtained were largely classified into two groups according to specificity to KML-C and ML-I, a pectin from European mistletoe. One group mAbs (9H7-D10 and 3C2-lH4) strongly reacted with KML-C, but not ML-I. In contrast, another group cAbs (8Bll-2C5, BE12-3E9 and 5E10-Fl) reacted with both KML-C and ML-1. The subisotypes of these mobs were shown to be IgGl (9H7-lD10, 3C2-lH4 and 8Bll-2C5) or IgM (8E12-3E9 and 5E10-Fl). To develop an assay system for determination of the amount of KML-C, we established the sandwich ELISA (enzyme-linked immunosorbent assay) method using these mAbs and horse radish peroxidase (HRP)-labelled cAbs. In various combinations of the cAbs for coated antibody and detection antibody, the sandwich ELISA quantitatively detected KML-C, showing the detection limit ranging from 7-5,000 ng/ml. Especially reproducibility (C.V) of the sandwich ELISA, in which 8E12-3E9 was used for coating antibody and 8Bll-2C5-HRP for detection antibody, was 4.59-5.83 in intra assay, and 3.9-9.4 in inter assay.

• Perinatology
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• 제29권4호
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• pp.165-169
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• 2018

Objective: Highly sensitive haptoglobin measurement should be used in neonates because the haptoglobin concentration in neonates is lower than that of adults. The aim of this study was to establish the reference values of haptoglobin levels in the cord blood of uninfected neonates. Methods: The cord blood of 29 preterm and 51 term babies was collected, and data from the mother and the newborn were recorded. The haptoglobin concentrations of 80 cord blood samples were simultaneously measured by enzyme-linked immunosorbent assay (ELISA; Assaypro, St Charles, MO, USA) and immunoturbidimetry assay (Roche Diagnostics, Basel, Switzerland). C-reactive protein (CRP) was also measured by immunoturbidimetry assay (Roche Diagnostics, Switzerland). Results: Mean values of CRP and ELISA haptoglobin were not significantly different between preterm and term babies. The 2.5 percentile and 97.5 percentile values of ELISA haptoglobin concentration were as follows: 80 neonates, 0.01 mg/dL and 0.59 mg/dL; 29 preterm babies, 0.08 mg/dL and 0.18 mg/dL; and 51 term babies, 0.07 mg/dL and 0.23 mg/dL. There were no differences in ELISA haptoglobin concentration according to maternal underlying diseases, delivery method, usage of antibiotics or steroids before delivery, gestational age, gender of baby, or twin gestation. Conclusion: A highly sensitive haptoglobin method should be used to determine the haptoglobin concentration in Korean newborns because the reference values of cord blood haptoglobin concentration in Korean newborns are less than the lower detection limit for commonly used immunoturbidimetric haptoglobin measurement methods.

• 한국식물병리학회지
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• 제14권2호
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• pp.130-135
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• 1998

This study was carried out to detect cymbidium mosaic potexvirus (CymMV) and odontoglossum ringspot tobamovirus (ORSV) in cultivated orchid plants in Korea. The standard double antibody sandwich enzyme-linked immunosorbent assay (ELISA) and reverse transcription polymerase chain reaction (RT-PCR) were carried out for detection of the viruses in the collected orchid samples. ELISA was suitable for massive-scale diagnostic method for virus detection in orchids. RT-PCR was rapid, time-saving and reliable detective method, and detection limit data showed that RT-PCR was 103 times more sensitive than ELISA. Of the 321 individual orchids representing 5 orchids genera tested by the ELISA, CymMV and ORSV were detected in 15.6% and 22.4%, and mixed infection of the both viruses with 4.9%, respectively. Of the Cymbidium plants tested, cultivated plants showed 52.5% virus infection rate with either CymMV or ORSV and both viruses.

• Food Science and Biotechnology
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• 제17권3호
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• pp.623-630
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• 2008

A non-instrumental immunochromatographic (ICG) strip-test and direct competitive enzyme-linked immunosorbent assay (DC-ELISA) for aflatoxin B1 (AFB1) determination were developed and optimized. The detection limits of ICG strip-test and DC-ELISA were 0.5 and 0.004 ng/mL, respectively, and these methods possessed a cross-reaction to aflatoxins. The results of spiked samples by both methods were coincided with the amount spiked AFB1 and the comparative analyses of 172 real samples by 2 immunoassays and high performance liquid chromatography (HPLC) showed a good agreement. Especially, the ICG strip-test is easier to perform and quicker, but less sensitivity than DC-ELISA. Both methods could analyze a high sample throughput with short time, but the sample throughput of ICG strip-test was better. Therefore, the ICG strip-test can be used as a simple, easy, non-instrumental, and fast screening technique for AFB1 determination.

• 대한수의학회지
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• 제40권1호
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• pp.81-85
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• 2000

Coxiella burnetii (C burnetii) is the causative agent of Q fever in animal and human. The distribution of the disease has been documented around world. In this study we developed the competitive enzyme linked immunosorbent assay(cELISA) and compared it with indirect immunofluorescent assay(IFA). A monoclonal antibody(Mab) against C burnetii and a peroxidase-conjugated anti-mouse IgM were used as an indicator system competing against antibody in animal serum or as an indicater of the absence of antibody. Sera were considered antibody positive when the percentage inhibition index(PI index) is upper than 30. PI index is calculated as 100-[sample OD/Mab OD)${\times}100$]. Among 162 bovine serum samples, 23 samples were antibody positive both in cELISA and IFA. And 156 samples showed same results. From goat with experimentally induced infection with C burnetii the antibody was detected 20 days early in cELISA compared to IFA. On the basis of present findings, it was demonstrated that cELISA is a reliable diagnostic method for The detection of specific antibodies against C burnetii infection.

• Animal Bioscience
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• 제34권12호
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• pp.1995-2002
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• 2021

Objective: Detection of adulteration in processed meats is an important issue for some countries due to substitution of beef with a cheaper source of protein like poultry. In this study, the presence of chicken meat was investigated using real-time polymerase chain reaction (real-time PCR) and enzyme-linked immunosorbent assay (ELISA) techniques to verify adulteration of fermented sausage samples. Methods: A total of 60 commercial samples were collected from 20 establishments in three replicates including 10 fermented sausage manufacturers and 10 butchers to investigate the presence of chicken meat with the sequential use of real-time PCR and ELISA techniques. In addition, pH, moisture content, water activity and color values of the samples were determined. Results: Both real-time PCR and ELISA showed agreement on the presence or absence of chicken meat in 55 out of 60 fermented sausage samples and chicken meat was identified with both methods in 16 samples. Five samples produced inconsistent results for the presence of chicken meat in the first run. Nevertheless, the presence of chicken meat was verified with both methods when these samples were analyzed for the second time. In addition, the average physico-chemical values of the fermented sausage samples tested positive for chicken meat were not significantly different from some of those fermented sausage samples tested negative for the chicken meat. Conclusion: The sequential use of real-time PCR and ELISA techniques in fermented sausages could be beneficial for the government testing programs to eliminate false negatives for detection of adulteration with chicken meat. Furthermore, consumers should not rely on some of the quality cues including color to predict the adulteration of fermented sausages with chicken meat since there were no statistical differences among some of the samples tested positive and negative for chicken meat.

• 대한의생명과학회지
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• 제3권2호
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• pp.115-123
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• 1997

인간 $\alpha$-fetoprotein (AFP)은 간암, 위암, 생식기 종양 및 신경관 이상인 환자를 검사하고 진단하는데 유용한 지표로 알려져 있다. 본 연구에서는 사람의 AFP를 분리정제 하여 폴리클로날 항체를 생산하고 인간 혈장과 양수내의 AFP를 측정하기 위한 경쟁적 효소면역 분석법을 개발하고자 하였다. 친화크로마토그래피법과 SDS-polyacrylamide 전기영동법을 이 용하여 양수로부터 AFP를 분리하였다. 정제된 AFP를 토끼에 주사하여 폴리클로날 항체를 생산하였으며, 이중면역확산법과 Western blot 분석법을 사용하여 본 연구실에서 제조된 항체의 항원 특이성이 대단히 높음을 확인하였다. AFP와 항혈청을 이용하여 표준곡선을 얻었으며, 민감도는 5ng/ml이었고, 작용범위는 5~l,000ng/ml이었다. 분석내 CV는 4.5%이었고, 분석간 CV는 8.5%이었다. 따라서 이러한 결과로 보아 본 연구에서 개발된 경쟁적 효소면역분석법이 AFP를 측정하기에 적절하며, 간암 등의 기초연구에도 많은 기여를 할 것으로 생각된다.