• 제목/요약/키워드: Antibody titer

검색결과 436건 처리시간 0.022초

Mycoplasma pneumoniae 유행 시기(2003년 하반기)의 항체 양전율에 대한 조사 (A Study of Antibody Conversion Rate During a Mycoplasma pneumoniae Epidemic Period(the Second Half of 2003))

  • 김도균;유진호;유영;고영률
    • Clinical and Experimental Pediatrics
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    • 제48권5호
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    • pp.500-505
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    • 2005
  • 목 적 : 소아 호흡기 감염의 주된 병원체인 M. pneumoniae는 일반적으로 4 내지 7년의 유행 주기를 가지는 것으로 알려져 있으나 M. pneumoniae 유행 기간 중 항체 양전율에 대한 정확한 국내 보고는 아직까지 없는 실정이다. 이에 저자들은 2003년 하반기 M. pneumoniae 유행 기간 전후로 항체 추적 검사를 시행하여 항체 양전율을 조사하고 나이, 초기 항체가, 아토피 유무가 항체 양전율에 미치는 영향을 알아보고자 본 연구를 시행하였다. 방 법 : 2003년 상반기 본원 외래를 방문하여 Mycoplasma 항체를 측정한 환아 중 혈청 항체가가 음성, 1 : 40, 1 : 80이었던 환아 191명을 대상으로 2004년 상반기에 추적 검사를 실시하였다. 추적 검사상 항체 역가가 4배 이상 증가한 경우를 항체 양전으로 정의하였고 항체 양전 여부에 따라 항체 양전군과 항체 비양전군으로 구분하였다. 혈청 항체 검사는 Serodia-Myco II 입자 응집법을 사용하여 시행하였다. 결 과 : 대상 환아들의 평균 나이는 $6.6{\pm}2.7$세였다. 남여 수는 각각 137명과 54명이었고 4세 이상 환아 중 아토피로 분류된 환아는 75명(44.6%)이었다. 대상 환아 중 항체 양전을 보인 환아는 83명(43.5%)이었다. 항체 양전군과 비양전군의 나이, 성별, 아토피 유무를 각각 비교하였을 때 두 군간의 유의한 차이는 보이지 않았다. 대상 환아들을 나이에 따라 네 군으로 나누어 비교하였을 때 각 군 사이 유의한 항체 양전율의 차이는 없었다. 초기 항체가가 음성, 1 : 40, 1 : 80이었던 환아들에서 항체 양전율은 각각 45.5%, 46.3%, 26.1%로 각 군 간 항체 양전율의 유의한 차이는 보이지 않았다. 아토피군과 비아토피군으로 나누어 비교하였을 때 항체 양전율은 각각 40.0%, 48.4%로 통계적으로 유의한 차이는 관찰되지 않았다. 결 론 : 2003년 하반기의 M. pneumoniae 유행 시기에 항체 양전율은 43.5%로 관찰되었으며 나이, 초기 항체가, 아토피 유무에 따른 항체 양전율의 차이는 없었다. 위 결과로 미루어 보아 M. pneumoniae 유행 시기에 소아 연령의 상당수에서 M. pneumoniae 감염에 이환되는 것으로 생각되며 M. pneumoniae의 혈청학적 역학 연구에 항체 양전율 조사가 유용하게 쓰일 수 있을 것으로 사료된다.

경북지방유래 추백리 양성계에서의 균분리 및 혈청역가 추이 (The variation of serological titers on the chickens infected pullorum disease from Kyongbuk provinces)

  • 김영환;김경희;우용구;장영술;조민희;김수웅
    • 한국동물위생학회지
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    • 제20권1호
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    • pp.19-26
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    • 1997
  • The present study was conducted to investigate the general epidemiological situations with 18-pullorum infected chickens from Kyongbuk provinces during the period from June 1995 to January 1996. On the Salmonella pullorum isolation tests by rectal swab culture method from infected chickens (386-samples), any Salmonella spp was not isolated from infected live-birds. But 2-S pullorum were isolated of 2-dead chickens(33.3% ) from 6-dead chickens which were positively reacted by serological tests. On the other hand, we could not isolated any Salmonella spp. in any parts of egg-contents ; egg-shell, egg-white and egg-yolks with 25-infected bird eggs. On the tests of antibiogram, 2-S pullorum strains were highly sensitive to GM, AM, SXT, CZ, K, FIM, ENR, C, AN, N, NN, LIN+SP, CF, TE and PB, respectively and intermediate sensitive to the CB, CFP, CL, S, P and XNL. But 2-strains were resistant to CC, DP, E, L, OX, TLA and TyLO. In the serological tests, pullorum antibody titers of 18-infected birds was from 2.76 to 9.18 with average by the microplate test. During the 6-months, pullorum antibody average titers were not changed generally. To validate the effects of the antimicrobial agent treatments to the serological antibody titers, infected 6-chickens was medicated with 0.5%-futazolidone. The titer of premeditated birds was average 4.26 but after medication with furazolidone, the titers of treated 6-birds was average 4.08.

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추백리의 혈청학적 진단법에 관한 연구 (Studies on serological tests for pullorum disease)

  • 김정태;심항섭;김태종;고태오;우종태;유기승;박유순
    • 한국동물위생학회지
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    • 제21권3호
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    • pp.313-323
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    • 1998
  • In order to establish a sensitive and specific diagnostic method for detection of antibody to Salmonella pullorum, a enzyme-linked immunosorbent assay(ELISA) was designed and standardized. The diagnostic efficacy of the established ELISA was compared with that of the serum plate agglutination test and immunodiffusion test for pullorum disease. 1. The chicken hyperimmune sera to Salmonella pullorum, S gallinarum, S typhimurium and S typhi were shown the cross reaction to S pullorum antigen by serum plate agglutination test. 2. When compared the cross reaction titer of microplate agglutination test for chickens hyperimmune sera, it was found that the titer were 64 in S pullorum, 32 in S gallinarum, 4 in S typhimurium and 8 in S typhi, respectively. 3. When compared the specificity of various antigen(HA, EA, PA and SA) by the immunodiffusion test, the most suitable antigen was phenol-treated bactrium. 4. The optimal concentration of S pullorum antigen for ELISA was 1 : 160 dilution of bacterium. 5. The efficacy of the ELISA for detection of S pullorum antibody was compared with serum Plate agglutination test and immunodiffusion test in chickens infected with S pullorum. The antibody was first detected at 6 days after infection using three tests examined. The antibody was alldetected at 9 days by ELISA, at 12 days by serumplate agglutination test, at 15 days by immunodiffusion test.

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Virus 중화시험법에 의한 닭 빈혈성인자의 항체조사 (Survey of antibody to chicken anemia agent by virus neutralization test)

  • 류광선;고홍범
    • 대한수의학회지
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    • 제33권2호
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    • pp.227-234
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    • 1993
  • A serological survey for antibody to chicken anemia agent(CAA) was carried out by virus neutralization test. Antibody to CAA was detected in broilers and layers at different age groups. The results obtained were summarized as follows ; 1. Of a total of 1,035 chicken sera from 1.16 flocks 617 samples of sera were detected as positive(59.6%) and 95 flocks of a total flocks as positive(81.9%). 2. Proportion of positive sera by age were 92.3 %(88.9~100%) at 1 to 2 weeks of age, 56.4%(16.7~77.8%) at 3 to 9 weeks of age, 85.0%(50.0~100%) at 10 to 14 weeks of age and all tested sera were positive at over the 15 weeks age. 3. In each broiler and layer chicken 63.6% and 68.4% chicks possessed positive sera respectively. 4. Neutralizing antibody titer in age group was various from 1:10 to 1:6,400 and mean titer was 1:400 to 1:800.

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Immunological Properties of Recombinant Hepatitis B Surface Antigen Expressed in Mammalian Cell(C127)

  • Lee, Young-Soo;Kim, Byong-Kak;Choi, Eung-Chil
    • Archives of Pharmacal Research
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    • 제21권5호
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    • pp.543-548
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    • 1998
  • We examined the immunological properties of the recombinant hepatitis B surface antigen (r-HBsAg) which was expressed in mammalian cell (C127). The cross-immunity of r-HBsAg and plasma-derived hepatitis B surface antigen (p-HBsAg) were tested using Western blotting and ELISA with guinea pig polyclonal antibody and naturally infected human-derived antibody and the both antigens show the same results in their response pattern and intensity, which indicate they have a good cross-immunity. from the measurement of $ED_{50}$ after formalin- or heat-inactivation, both r-HBsAg and p-HBsAg and p-HBsAg showed $ED_{50}$ of 0.2-0.3 in formalin-inactivaton, while r-HBsAg was 0.05-0.09 and p-HBsAg was 0.03-0.07 in heat-inactivation, which means heat-inactivation method is 3-4 times superior in immunogenicity. In the immunopersistency test performed in guinea pig for the period of 3 months with two different adjuvants, antibody titer was 34.2 with muramyl dipeptide adjuvant, which was 1.8 times greater than the antibody titer of 18.9 with $AIPO_{4}$ adjuvant. the mutagenicity of r-HBsAg has the same cross-immunity with p-HBsAg, and heat-inactivation method and muramyl dipeptide adjuvant allow development of r-HBsAg vaccine with excellent immunogenicity.

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동물원 동물에서 백신접종 후 구제역바이러스(O형) 구조단백질 항체가 분석 (Analysis on antibody titer of structural protein after vaccination against foot-and-mouth disease virus (Type O) in zoo animals)

  • 이현호;어경연
    • 한국동물위생학회지
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    • 제45권2호
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    • pp.125-131
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    • 2022
  • The purpose of this study was to examine antibody titers to structural protein (SP) of the foot-and-mouth disease (FMD) virus after vaccination in animals of the Seoul zoo. After the initial inoculation of FMD vaccine to the susceptible animals of the zoo, a total of 235 blood samples were collected from 42 species of zoo animals during treatment or necropsy. All samples were tested by using enzyme-linked immunosorbent assay (ELISA). The overall positive rate of SP antibodies against FMD virus was 94.0% (221/235). However, the positive rates varied according to animal species. The results of positive rates in 30 species were 100% but in 12 species were 50-94.7%. We showed that most animals that have received FMD vaccine in Seoul zoo have been reached to the level of herd immunity against FMD virus after the vaccination. To the best of our knowledge, this study would be the first report for monitoring the vaccine-induced SP antibody titers against FMD virus after vaccination in various zoo animal species in Korea.

전남지방의 소 합포체성 폐렴바이러스(Bovine Respiratory Syncytial Virus) 감염에 관한 혈청학적 연구 (Seroepidemiological Studies on Bovine Respiratory Syncytial Virus of Cattle in Chonnam Province)

  • 이채용;이강복;이정길;이정치;김상기;조재진
    • 한국임상수의학회지
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    • 제17권1호
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    • pp.45-51
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    • 2000
  • Sera from 425 Korean native and 203 Holstein cattle were collected from October 1994 to September 1995 from dairy farms and slaughterhouses in Chonnam province to study the exposure rate to bovine respiratory syncytial virus(BRSV). Serum antibody titers against BRSV were measured by neutralization test, and results were as follows: Overall prevalence of seropositive cattle to BRSV were 74.5%, and the exposure rate to BRSV was higher among the Holstein (77.3%) than among the Korean native cattle(73.2%). The serum antibody titers against BRSV ranged from 1:2~$\geq$1:256 in both species. Among Korean native cattle, the most frequent serum antibody titer was 1:4 against BRSV(19.3%), while only 1.4% of seropositive cattle had serum titer of $\geq$1: 256. Among Holstein cattle, 22.7% of examined cattle contained serum titer of 1:8, while 1.5% of seropositive cattle showed $\geq$ 1:256. Antibody titers against BRSV were higher among males than females in both Holstein (82.1% vs. 73.1%) and Korean native (74.5% vs. 69.2%) cattle. Prevalence of seropositive cattle by age in both species were evenly distributed, although the highest number (76.9%) of seropositive were at the age of 3 in Korean native cattle, while 83.5% of seropositive Holstein cattle were of 2 years old. The lowest seropositive rate was observed in cattle of less than 1 year old(25.0%). Seasonal occurrunce of BRSV was the highest in spring season in both Holstein (86.6%) and Korean native (81.0%) cattle (P<0.05).

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Effects of infectious bursal disease virus(IBDV) and newcastle disease virus(NDV) vaccines on performance of broiler chicks

  • Kwon, Jung-taek;Kim, Tae-joong;Ryu, Kyeong-seon;Song, Hee-jong
    • 대한수의학회지
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    • 제39권4호
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    • pp.738-742
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    • 1999
  • The objective of this experiment was to investigate the effect of Newcastle disease virus (NDV) and infectious bursal disease virus (IBDV) vaccination on performance of broiler chicks for five weeks. Two types of poultry houses and three patterns of vaccination ($NDV^-/IBDV^-$, $NDV^+/IBDV^-$ and $NDV^+/IBDV^+$) were factorially assigned to six treatments. NDV, B1 strain and IBDV, Bursin-2 vaccine were orally administered at 5, 14 and 7, 18 days, respectively. Forty eight hundred chicks were grouped into four replications with two hundnyd hybro $\times$ hybro chicks per each treatment. Weight gain, feed conversion ratio (FCR), mortality and product index were surveyed at the end of experiment. Bursa index and IBDV antibody titer of chicks were weekly measured. Weight gain of chicks vaccinated with $NDV^+/IBDV^+$ was significantly increased compared to that of other treatments at both window and windowless poultry houses (p<0.05). Chicks vaccinated with $NDV^+/IBDV^+$ also showed significantly improving the FCR and mortality compared to those of other treatments at both poultry houses (p<0.05). The bursa indecies of both poultry houses were high from one-day- to three-weeks-old, but were low for the rest of two weeks. IBDV antibody of all chicks was detected 100% by agar gel precipitation (AGP) test at one day old, but was not detected in $NDV^-/IBDV^-$ and $NDV^+/IBDV^-$ treatments at four weeks old. However, it showed 100% in $NDV^+/IBDV^+$ treatment. Antibody titer using ELISA showed similar trend to that of AGP test. The results of this experiment confirmed that IBDV and NDV combined vaccine significantly improved the performance of broiler chicks.

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Enzyme-linked immunosorbent assay를 이용한 국소적, 유년성 치주염 환자의 혈청내 Actinobacillus actinomycetemcomitans Y4 균주 항체역가에 관한 연구 (Enzyme-Linked Immunosorbent Assay for the detection of serum lgG and lgM Antibodies to Actinobacillus Actinomycetemcomitans Y4 in Localized Juvenile Periodontitis)

  • 정종평;정진형;최선진
    • 대한치과의사협회지
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    • 제22권1호통권176호
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    • pp.57-66
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    • 1984
  • Twelve patients of localized juvenile periodontitis were evaluated to detection of serum IgG and IgM antibodies to Actinobacillus actinomycetemcomitans Y4 strain. Sera were isolated from those patients. Antibody titer of patients sera to Aa stran Y4 strain. Sera were isolated from those patients. Antibody titer of patients sera to Aa stran Y4 were determined by modified enzyme-linked immunosorbent assey (ELISA) using sonicated and formalin-fixed whole Aa y4 strain for detection of serum IgG and IgM antibody titers. To compare with health control and L.J.P., we used 12 healthy dental student who did not exhibited any gingivits. Results were determined by using ELISA reader at 400mm absorbance value. Data analysis were performed with comparison of the regression functions relating absorbance to dilution and Dunnett t-test. Significant high antibody titer to As Y4 in L.J.P. sera were shown in this examination(281. 4 Eu-G to 162.80 Eu-G, 106.0 Eu-M to 40.0 Eu-M for sonicated As Y4 antigen and 653.960. to 138.117 Eu-M for intact As Y4) and this data were also statistically significant (P<0.05). This work was supported in part from Seoul national University Hospital Grant and Korean Science Foundation.

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The optimization of ELISA for methamphetamine determination : the effect of immunogen, tracer and antibody purification method on the sensitivity

  • Choi, Jeongeun;Choi, Myung-Ja;Kim, Choonmi;Cho, Young-Shik;Chin, Jaeho;Jo, Young-Ah
    • Archives of Pharmacal Research
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    • 제20권1호
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    • pp.46-52
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    • 1997
  • To obtain more sensitive immunoassay for methamphetamine (MA) determination, the optimum condition of enzyme-linked immunosorbent assay (ELISA) was investigated in regard to immunogens, antibody purification methods and coating tracers. Activated MA, N-(4-aminobutyl)methamphetamine (4-ABMA), was conjugated with bovine serum albumin (BSA) or keyhole limpet hemocyanin (KLH) and used as immunogen. The antibodies were purified by protein G chromatography or various immunoaffinity chromatography-linked MA-protein ligands, such as MA-BSA, MA-KLH or MA-ovalbumin (OVA). Each purified antibody was characterized by means of sensitivity and cross-reactivity using the three MA-protein coating tracers, MA-BSA, MA-KLH and MA-OVA. The best sensitivity of each antibody was acquired with the MA-OVA tracer although the tracer concentration and the antibody titer level at optimum condition were varied. The antibody with high titer level did not always yield good sensitivity. At optimum condition, immunoaffinity chromatography-purified antibodies were better for sensitivity and for specificity than protein G-purified antibodies. The cross-reactivity of the purified antibodies seemed to be affected by immunogen structure and showed somewhat different patterns according to the immunoaffinity ligand utilized. These data show that the antibody purification method as well as choice of coating tracer and immunogen is essential for the sensitivity and specificity of EIA; the optimum condition for assay should be discovered using various methods and combinations.

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