TY - JOUR
T1 - The humoral immune response to BCG vaccination
AU - Tanner, Rachel
AU - Villarreal-Ramos, Bernardo
AU - Vordermeier, H. Martin
AU - McShane, Helen
PY - 2019/6/11
Y1 - 2019/6/11
N2 - Bacillus Calmette Guérin (BCG) is the only currently available vaccine against tuberculosis (TB), but it confers incomplete and variable protection against pulmonary TB in humans and bovine TB (bTB) in cattle. Insights into the immune response induced by BCG offer an underexploited opportunity to gain knowledge that may inform the design of a more efficacious vaccine, which is urgently needed to control these major global epidemics. Humoral immunity in TB and bTB has been neglected, but recent studies supporting a role for antibodies in protection against TB has driven a growing interest in determining their relevance to vaccine development. In this manuscript we review what is known about the humoral immune response to BCG vaccination and re-vaccination across species, including evidence for the induction of specific B cells and antibodies; and how these may relate to protection from TB or bTB. We discuss potential explanations for often conflicting findings and consider how factors such as BCG strain, manufacturing methodology and route of administration influence the humoral response. As novel vaccination strategies include BCG prime-boost regimens, the literature regarding off-target immunomodulatory effects of BCG vaccination on non-specific humoral immunity is also reviewed. Overall, reported outcomes to date are inconsistent, but indicate that humoral responses are heterogeneous and may play different roles in different species, populations, or individual hosts. Further study is warranted to determine whether a new TB vaccine could benefit from the targeting of humoral as well as cell-mediated immunity.
AB - Bacillus Calmette Guérin (BCG) is the only currently available vaccine against tuberculosis (TB), but it confers incomplete and variable protection against pulmonary TB in humans and bovine TB (bTB) in cattle. Insights into the immune response induced by BCG offer an underexploited opportunity to gain knowledge that may inform the design of a more efficacious vaccine, which is urgently needed to control these major global epidemics. Humoral immunity in TB and bTB has been neglected, but recent studies supporting a role for antibodies in protection against TB has driven a growing interest in determining their relevance to vaccine development. In this manuscript we review what is known about the humoral immune response to BCG vaccination and re-vaccination across species, including evidence for the induction of specific B cells and antibodies; and how these may relate to protection from TB or bTB. We discuss potential explanations for often conflicting findings and consider how factors such as BCG strain, manufacturing methodology and route of administration influence the humoral response. As novel vaccination strategies include BCG prime-boost regimens, the literature regarding off-target immunomodulatory effects of BCG vaccination on non-specific humoral immunity is also reviewed. Overall, reported outcomes to date are inconsistent, but indicate that humoral responses are heterogeneous and may play different roles in different species, populations, or individual hosts. Further study is warranted to determine whether a new TB vaccine could benefit from the targeting of humoral as well as cell-mediated immunity.
KW - Antibodies
KW - B cells
KW - BCG vaccine
KW - Bovine TB
KW - Humoral immunity
KW - Tuberculosis
KW - Immunoglobulin E/biosynthesis
KW - Antibody Specificity
KW - Hypersensitivity, Immediate/prevention & control
KW - Autoantibodies/biosynthesis
KW - Mycobacterium bovis/immunology
KW - Mycobacterium tuberculosis/immunology
KW - Immunomodulation
KW - Humans
KW - Tuberculosis, Pulmonary/immunology
KW - Tuberculosis, Bovine/immunology
KW - B-Lymphocytes/immunology
KW - Animals
KW - BCG Vaccine/administration & dosage
KW - Immunity, Humoral
KW - Cancer Vaccines/immunology
KW - Cattle
KW - Antibodies, Bacterial/biosynthesis
UR - http://www.scopus.com/inward/record.url?scp=85068922673&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2019.01317
DO - 10.3389/fimmu.2019.01317
M3 - Review Article
C2 - 31244856
AN - SCOPUS:85068922673
SN - 1664-3224
VL - 10
JO - Frontiers in Immunology
JF - Frontiers in Immunology
IS - JUN
M1 - 1317
ER -