BCG vaccine in Korea

被引:17
作者
Joung, Sun Myung [1 ]
Ryoo, Sungweon [1 ]
机构
[1] Korean Natl TB Assoc, Korean Inst TB, 168-5 Osongsaengmyeong 4 Ro, Cheongwon 363954, South Korea
关键词
BCG vaccine; Korea; Tuberculosis;
D O I
10.7774/cevr.2013.2.2.83
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The anti-tuberculosis Bacille de Calmette et Guerin (BCG) vaccine was developed between 1905 and 1921 at Pasteur Institutes of Lille in France, and was adopted by many countries. BCG strains comprise natural mutants of major virulence factors of Mycobacterium tuberculosis and that BCG sub-strains differ markedly in virulence levels. The tuberculosis became endemic in Korea after the Korean War (1950s). The BCG strain, which was donated by Pasteur Institutes, was brought to Korea in 1955, and the first domestic BCG vaccine was produced by the National Defense Research Institute (NDRI), current Korea Centers for Disease Control and Prevention (KCDC), in 1960. Since 1987, BCG manufacture work was handed over to the Korean Institute of Tuberculosis (KIT), the freeze-dried BCG vaccine was manufactured at a scale required to meet the whole amount of domestic consumption. However, since 2006, the manufacture of BCG vaccine suspended and the whole amount of BCG was imported at this point of time. Now KIT is planning to re-produce the BCG vaccine in Korea under the supervision of KCDC, this will be render great role to National Tuberculosis Control Program (NTP) and provide initiating step for developing new tuberculosis vaccines in Korea.
引用
收藏
页码:83 / 91
页数:9
相关论文
共 64 条
[21]   BCG VACCINATION IN DENMARK [J].
HOLM, J .
PUBLIC HEALTH REPORTS, 1946, 61 (36) :1298-1315
[22]   Identification of two subpopulations of Bacillus Calmette-Guerin (BCG) Tokyo172 substrain with different RD16 regions [J].
Honda, I ;
Seki, M ;
Ikeda, N ;
Yamamoto, S ;
Yano, I ;
Koyama, A ;
Toida, I .
VACCINE, 2006, 24 (23) :4969-4974
[23]   The primary mechanism of attenuation of bacillus Calmette-Guerin is a loss of secreted lytic function required for invasion of lung interstitial tissue [J].
Hsu, T ;
Hingley-Wilson, SM ;
Chen, B ;
Chen, M ;
Dai, AZ ;
Morin, PM ;
Marks, CB ;
Padiyar, J ;
Goulding, C ;
Gingery, M ;
Eisenberg, D ;
Russell, RG ;
Derrick, SC ;
Collins, FM ;
Morris, SL ;
King, CH ;
Jacobs, WR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12420-12425
[24]  
HYGE TAGE V., 1956, ACTA TUBERC SCAND, V32, P89
[25]   A CONTACT STUDY TO EVALUATE THE BCG VACCINATION PROGRAM IN SEOUL [J].
JIN, BW ;
HONG, YP ;
KIM, SJ .
TUBERCLE, 1989, 70 (04) :241-248
[26]   Supplementation with RD antigens enhances the protective efficacy of BCG in tuberculous mice [J].
Kalra, Mamta ;
Grover, Ajay ;
Mehta, Neena ;
Singh, Jaspreet ;
Kaur, Jaspreet ;
Sable, Suraj B. ;
Behera, Digambar ;
Sharma, Pawan ;
Verma, Indu ;
Khuller, G. K. .
CLINICAL IMMUNOLOGY, 2007, 125 (02) :173-183
[27]   Warning: Differences in the copy number of duplication unit 2 (DU2) within BCG Danish 1331 may influence findings involving genetically modified BCG Danish strains [J].
Kernodle, Douglas S. .
VACCINE, 2012, 30 (42) :6013-6014
[28]   Novel genome polymorphisms in BCG vaccine strains and impact on efficacy [J].
Leung, Andrea S. ;
Tran, Vanessa ;
Wu, Zuowei ;
Yu, Xuping ;
Alexander, David C. ;
Gao, George Fu ;
Zhu, Baoli ;
Liu, Jun .
BMC GENOMICS, 2008, 9 (1)
[29]   Deletion of RD1 from Mycobacterium tuberculosis mimics bacille Calmette-Guerin attenuation [J].
Lewis, KN ;
Liao, RL ;
Guinn, KM ;
Hickey, MJ ;
Smith, S ;
Behr, MA ;
Sherman, DR .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (01) :117-123
[30]   EVIDENCE FOR ABSENCE OF THE MPB64 GENE IN SOME SUBSTRAINS OF MYCOBACTERIUM-BOVIS BCG [J].
LI, HY ;
ULSTRUP, JC ;
JONASSEN, TO ;
MELBY, K ;
NAGAI, S ;
HARBOE, M .
INFECTION AND IMMUNITY, 1993, 61 (05) :1730-1734