• Title/Summary/Keyword: 백신항체가

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강병원성 AI(H5N1), 백신과 살처분 병용정책을$\cdots$

  • 한희
    • KOREAN POULTRY JOURNAL
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    • v.36 no.2 s.412
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    • pp.99-105
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    • 2004
  • 백신은 엄격한 정부 통제하에 관리가 제대로 될 수 있는 농가 및 발생지역과 인근위험지역에 한해 공급하되 백신을 공급한 지역 수의사는 접종계군이 도태시까지 혈액을 채취하여 검역원에 보내 감염항체인지 백신접종 항체인지 구분하되 백신접종계군도 감염항체가 나타나면 살처분하고 백신접종항체군은 남겨두어 피해를 최소화한다. 그리고 질병발생 종료시에는 백신공급을 중단하여 질병의 토착화를 막는 철저한 관리가 필요하다.

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IBD 모체이행항체가 있는 병아리의 생독백신 사용법

  • 서창희
    • KOREAN POULTRY JOURNAL
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    • v.27 no.8 s.310
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    • pp.140-143
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    • 1995
  • 모체이행항체를 가지고 있는 병아리에 IBD백신을 접종할 때에는 다음과 같은 사항을 유의하여 실시한다. -1일령 병아리에 백신을 접종할 때에는 최소한 2번 접종한다. 2차접종은 2-3주령에 실시해야 한다. 우리나라의 경우 병아리의 모체이행할체 수준이 높기 때문에 2주령에 1차접종을 하고 4주령에 2차접종을 하는 것을 권하고 있다. -백신제조용 바이러스는 약독이나 중간독주를 사용해야 한다. 미국의 경우 모체이행항체가가 높은 병아리에 강독으로 제조한 백신을 사용하는 경우가 있는데 이는 바람직하지 못하다. -농장의 실질적인 위생상태가 백신프로그램의 효과를 증대시키는데 효과가 있다. -항원성이 다른 IBD변이주가 입증된 지역에서는 약독화 시킨 변이주 바이러스를 혼합한 백신의 사용도 고려해 보아야 한다. 다행히 우리나라에서는 IBD변이주 바이러스는 입증된바가 없다.

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백신 프로그램의 디자인과 면역의 기본 원리

  • 대한양계협회
    • KOREAN POULTRY JOURNAL
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    • v.29 no.9 s.335
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    • pp.168-173
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    • 1997
  • 효과적인 백신 프로그램을 디자인하기 위해서는 질병과 면역에 대한 기본적인 이해가 필수적이다. 면역에 대해서 이해하기 위해서는 크게 체액성 면역과 세포성 면역으로 구분하여 이해하는 것이 유용할 수 있으며, 또한 이 두 가지 기전은 서로 상호협동적으로 작용한다는 사실을 이해하여야 한다. 숙주동물(닭)이 병원체이든 백신이든 일단 항원에 한 번 노출이 되면 이를 기억하는 기억 세포를 생성하여 두 번째 노출되었을 때 폭발적인 면역반응이 일어나도록 한다. 순환항체가 형성이 되면, 이 항체는 난황을 통하여 후대 병아리에게 전달될 수 있다. 면역의 형성은 백신이 가진 항원의 특성과 백신의 타입(생독, 사독)에 따라 다른 방식으로 나타난다. 면역에 대한 기본적인 개념을 충분히 숙지하고 다음의 사항을 고려하면 효과적인 백신 프로그램을 선택하기가 용이하다. (1) 전례 : 어떤 프로그램이 효과적이었는가? (2) 질병 : 어떤 질병이 문제가 되고 있는가? (3) 균주 : 균주의 차이는 중요한가? (4) 관리 : 백신의 사용을 불필요하게 할 효과적인 사양관리가 이루어질 수 있는가? (5) 모체이행항체 : 모체이행항체가 적절한 방어력을 가질 수 있을까? (6) 면역증강효과 : 그 중요성과 접종시기가 숙지되어 있는가? (7) 접종기술 : 접종기술에 문제가 있는데 프로그램이 제대로 효과를 발휘할 수 있을까?

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Study on Production of Antibody in Milk Immunized Cows with Some Helicobacter pylori Antigen (Helicobacter pylori 항원을 이용한 면역우유 생산에 관한 연구)

  • Park, Chang-Ho;Kim, Soo-Jung;Yea, Eon-Ju;Bae, Man-Jong
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.34 no.4
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    • pp.484-488
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    • 2005
  • This study has been to produce of anti-H. pylori antibody in milk produced from cows immunized with antigen of Helicobacter pylori and to search the relationship between vaccine dosage and antibody formation and impact of vaccine dosage on cows. The content of anti-H. pylori antibody in serum and whey increased in accordance with vaccine dosage volume. It has been confirmed that the formation of high-quantified antibody was produced in all groups with vaccine dosages of 10 mL, 20 mL and 30 mL. It has been turned out that the antibody was formed most in 20 mL dosage. It was inclined to $12\%$ reduce caused by vaccine injection, but recovered after about maximum 1 week. In measurement of body temperature of cows after vaccine injected, it was inclined to rise with the normal scope in comparison with the controlled conditions.

Preparation and Immunogenicity of the Combined Vaccine Composed of the Polysaccharide Capsule of Samonella typhi and Japanese Encephalitis Virus (장티푸스 협막 다당체와 일본 뇌염 바이러스의 혼합 백신 제조 및 면역성)

  • 김을제;지희윤
    • KSBB Journal
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    • v.19 no.1
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    • pp.88-92
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    • 2004
  • The immunogenicity of investigational combined vaccine, composed of the Japanese encephalis virus(JEV) and the polysaccharide capsule(Vi) of Salmonella typhi covalently bound to tetanus toxoid(TT) was evaluated in mice. The mice immunized with combined vaccine elicited higher anti-Vi Immunoglobulin G(IgG) as well as anti-JEV IgG levels than the mice immunized with Vi-TT or JEV alone. The combined vaccine produced four-fold increase in anti-Vi IgG level than Vi-TT alone. In JEV the combined vaccine was significantly more immunogenic than JEV alone and induced six-fold increase in IgG level. Adsorption of combined vaccine onto aluminium hydroxide gel also enhanced IgG level for both Vi and JEV.

Serological Response of Pups to the Selected Canine Vaccines and Vaccination Schedules against Canine Parvovirus (Canine parvovirus 함유 혼합백신들과 예방접종 스케줄에 따른 강아지의 혈청학적 반응)

  • Kim, Doo;Jeoung, Seok-young;Ahn, So-jeo;Jung, Jong-ho;Park, Son-il
    • Journal of Veterinary Clinics
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    • v.21 no.1
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    • pp.1-6
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    • 2004
  • This study was undertaken to provide the appropriate vaccination protocol of canine parvovirus (CPV) vaccine for the companion dogs in Korea. A total of 120 healthy pups (20 pups per group) at 6 weeks of age were randomly assigned to one of four commercially available vaccines [C, G, K, and V groups] and one of vaccination schedules [V2 and V4 groups]. The serological responses to the CPV component of the vaccines were determined by measuring HI titers. The maternal antibodies was declined to under the protective level at 6 weeks of age. Therefore, it was considered that vaccination of pups for CPV should be started at 6 weeks of age. And when the combination vaccine was used, the immunogenicity of V vaccine was superior to the other vaccines and optimum vaccination schedule was 3 times vaccination with 3 weeks-interval starting vaccination at 6 weeks of age. Although pups were vaccinated at 6 weeks of age, the geometric mean CDV titers of pups in all groups by 9 weeks of age were under the protective level. So, hygienic measures including avoiding to exposure to the high risk areas were needed to prevent CPV infection in this period.

Efficacy of Concurrent Administration of Live and Killed Newcastle Disease Vaccines in Day - Old Broiler Chicks (육용계 초생추에 대한 뉴켓슬병 생독 및 사독 백신의 동시접종 효과)

  • 최정옥;박승주;위성하
    • Korean Journal of Poultry Science
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    • v.15 no.3
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    • pp.193-198
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    • 1988
  • In order to examine the efficacy of concurrent vaccination with live and killed Newcastle disease(ND) vaccines two types of each live($B_1$ and LaSota) and killed(gel and oil) vaccines of all commercial origin were administered either alone or simultaneously to day-old broiler chicks having maternal antibody. Live vaccines were given by conjuntival instillation in volumes of 25${\mu}\ell$ containing $10^{6.0}$ to $10^{6.3}$ median embroy infective dose(EH)) while killed vaccines were given in 0.3$m\ell$ volumes subcutaneously at the back of the neck Hemagglutination inhibition(HI) antibodies were determined at weekly intervals until 8 weeks of age and protection rate was determined at 4 and 8 week of age by challenge inoculation with virulent ND virus(NDV). During the 8 weeks experimental period concurrent administration of live and oil vaccine produced the highest level of HI antibody and the most satisfactory protection, whereas concurrent rent vaccination with live and gel vaccine induced poor immune responses. There was no noticeable difference in the efficacy between the live vaccines, Bl and LaSota when simultaneously administered with oil vaccine. Except for oil vaccine, single administration of either live or killed vaccine at day-old produced less than 50% protection at 4 and 8 weeks postvaccination(PV). Oil vaucine alone induced 80% and 70% protection at 4 and 8 week PV, respectively. Concurrent vaccination caused on visible side reaction like respiratory symptoms and did not negatively influence the growth rate of birds until the end of experiment.

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Functional Immunity to Cross-Reactive Serotype 6A Induced by Serotype 6B in Pneumococcal Polysaccharide Vaccine (폐구균 다당질 백신 내 혈청형 6B에 의해 유도되는 교차 반응 혈청형 6A에 대한 기능적 면역)

  • Kim, Kyung Hyo
    • Clinical and Experimental Pediatrics
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    • v.48 no.5
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    • pp.506-511
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    • 2005
  • Purpose : Streptococcus pneumoniae serotype 6B and 6A are important pathogens in pneumococcal infections. It is commonly assumed that the 6B vaccines elicit antibodies cross-reacting with the 6A serotype and the cross-reactive antibodies protect against infections of 6A. To examine this assumption, we measured the opsonophagocytic capacity to serotype 6A and 6B in adults. Methods : Twenty-four adults were immunized with pneumococcal PS vaccine that contains 6B PS. Their preimmune and postimmune sera were studied for the capacity to opsonize 6B and 6A serotypes with opsonophagocytic killing assay. Results : Opsonization titers to 6B were significantly higher than those to 6A in preimmune and postimmune sera. Because significant increasesof opsonization titers were observed in adults with polysaccharide vaccines for 6A(cross-reactive) serotype as well as for 6B(vaccine) serotype, 6B PS in vaccine elicited cross-protective antibodies to 6A, but not in all cases. One adult did not have detectable levels of opsonization titers to 6A after immunization. Conclusion : Although 6B PS in pneumococcal PS vaccine elicits antibodies cross-reacting with 6A serotype in some adults, it may not occur always. This study should be extended to other age groups such as children and elderly people. The presence of the cross-protection should be directly determined in clinical trials of the pneumococcal vaccines as well as during the postlicensure monitoring surveys by serotyping the clinical isolates of pneumococci.

Analysis of Immunogenicity after Hepatitis B Vaccination in Korea by Literature Review (문헌 분석에 의한 B형 간염 백신의 항체 양전률의 비교)

  • Roh, Hye Ok;Lee, Woo Gill;Sohn, Young Mo
    • Pediatric Infection and Vaccine
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    • v.5 no.2
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    • pp.245-257
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    • 1998
  • Purpose : Although hepatitis B vaccine has been available to general population in Korea since 1983, it was difficult to compare various types of hepatitis B virus(HBV) vaccines primarily due to the differences in vaccination schedule, dosage, test methods and seropositive antibody level. In this study we reviewed the results of previous studies published in Korea, which include antibody positive rates and antibody titers of various vaccines, and examined the immunogenicity of these HBV vaccines. Methods : Studies published in medical journals, university journals concerning antibody positive rates following hepatitis B vaccination were reviewed. Inclusion criteria were those studies in which seroprotective antibody rate of 10mIU/mL or the sample ratio unit of 10 RU were used as the cut-off value and in which the test methods were RIA or ELISA. Exclusion criteria were; 1) unclear or inconsistent vaccine dosage, 2) no record of antibody titers or seroconversion rate, 3) no defined antibody rate or ratio for positive rating and 4) the vaccination schedule other than 0-1-2 months or 0-1-6 months. Results : 23 out of 52 studies were subjected for the review for seroconversion rates. 1) As for the immunogenicity in each age group, the seroconversion rates of Hepaccine(Cheil Jedang) were 85.1% in infants, 83.3% in children and 62.7% in adults, indicating higher rates in infants and children compared to adults(P<0.01). The seroconversion rates of Hepavax(Korea Green Cross) were 84.7%, 81.1% and 90.8%, indicating higher rates in infants and adults compared to children(P<0.01). 2) The seroconversion rate of Hepavax was 85.6% with 0-1-6 mo. schedule, 78.5% with 0-1-2 mo. schedule with a statistically significant difference(P<0.01). 4) There was no difference of seroconversion rates between the two doses of Hepavax, $5{\mu}g$ and $10{\mu}g$ in infants and children. 5) In adults the seroconversion rates were 62.7% with Hepaccine, 90.8% with Hepavax, and 94.8% with Engerix-B(SmithKline Beecham). Conclusion : In Korea, the incidence of chronic hepatitis B is high and changing the schedule in vaccination cannot contribute to the increase of the serocoversion rate. And in order to maximize immunogenicity, more effective vaccines as well as more proper vaccination methods should be used.

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일본에서 시판중인 오제스키병 생독백신의 유효성

  • Iwamura Y;Imamura T;Tokanaga E;Matsuo K
    • Journal of the korean veterinary medical association
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    • v.31 no.8
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    • pp.832-838
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    • 1995
  • 일본에서 시판되고 있는 4종류의 생독백신은 본병방어에 있어 어느 것이나 유효하다. 그러나 각기 백신의 성상은 각자 특성이 있음으로 유효성의 정도에 차이가 있다고 본다. 이런 관점에서 백신 유효성을 공격주를 바꾸어서 또한 이행항체 보유돈에서 비교 검토한 결과, 백신 D가 종합적으로 볼 때 가장 높고 다음 C, B, 최후의 A의 순이었다.

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