TY - JOUR
T1 - 100 years of Mycobacterium bovis bacille Calmette-Guérin
AU - Lange, Christoph
AU - Aaby, Peter
AU - Behr, Marcel A
AU - Donald, Peter R
AU - Kaufmann, Stefan H E
AU - Netea, Mihai G
AU - Mandalakas, Anna M
N1 - Copyright © 2022 Elsevier Ltd. All rights reserved.
PY - 2022/1
Y1 - 2022/1
N2 - Mycobacterium bovis bacille Calmette-Guérin (BCG), an experimental vaccine designed to protect cattle from bovine tuberculosis, was administered for the first time to a newborn baby in Paris in 1921. Over the past century, BCG has saved tens of millions of lives and has been given to more humans than any other vaccine. It remains the sole tuberculosis vaccine licensed for use in humans. BCG provides long-lasting strong protection against miliary and meningeal tuberculosis in children, but it is less effective for the prevention of pulmonary tuberculosis, especially in adults. Evidence mainly from the past two decades suggests that BCG has non-specific benefits against non-tuberculous infections in newborn babies and in older adults, and offers immunotherapeutic benefit in certain malignancies such as non-muscle invasive bladder cancer. However, as a live attenuated vaccine, BCG can cause localised or disseminated infections in immunocompromised hosts, which can also occur following intravesical installation of BCG for the treatment of bladder cancer. The legacy of BCG includes fundamental discoveries about tuberculosis-specific and non-specific immunity and the demonstration that tuberculosis is a vaccine-preventable disease, providing a foundation for new vaccines to hasten tuberculosis elimination.
AB - Mycobacterium bovis bacille Calmette-Guérin (BCG), an experimental vaccine designed to protect cattle from bovine tuberculosis, was administered for the first time to a newborn baby in Paris in 1921. Over the past century, BCG has saved tens of millions of lives and has been given to more humans than any other vaccine. It remains the sole tuberculosis vaccine licensed for use in humans. BCG provides long-lasting strong protection against miliary and meningeal tuberculosis in children, but it is less effective for the prevention of pulmonary tuberculosis, especially in adults. Evidence mainly from the past two decades suggests that BCG has non-specific benefits against non-tuberculous infections in newborn babies and in older adults, and offers immunotherapeutic benefit in certain malignancies such as non-muscle invasive bladder cancer. However, as a live attenuated vaccine, BCG can cause localised or disseminated infections in immunocompromised hosts, which can also occur following intravesical installation of BCG for the treatment of bladder cancer. The legacy of BCG includes fundamental discoveries about tuberculosis-specific and non-specific immunity and the demonstration that tuberculosis is a vaccine-preventable disease, providing a foundation for new vaccines to hasten tuberculosis elimination.
KW - Animals
KW - BCG Vaccine/adverse effects
KW - Cattle
KW - History, 19th Century
KW - History, 20th Century
KW - History, 21st Century
KW - Humans
KW - Mycobacterium bovis/immunology
KW - Tuberculosis, Bovine/epidemiology
KW - Vaccines, Attenuated/immunology
U2 - 10.1016/S1473-3099(21)00403-5
DO - 10.1016/S1473-3099(21)00403-5
M3 - Journal article
C2 - 34506734
SN - 1473-3099
VL - 22
SP - e2-e12
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 1
ER -