TY - JOUR
T1 - Updates on antibody functions in Mycobacterium tuberculosis infection and their relevance for developing a vaccine against tuberculosis
AU - Achkar, Jacqueline M.
AU - Prados-Rosales, Rafael
N1 - Funding Information:
JMA and RP-R and their discussed work are supported in part by the National Institutes of Health (NIH)/ National Institute of Allergy and Infectious Diseases [grant numbers AI127173 (JMA), AI117927 (JMA), and AI115091 (RP-R)] as well as by funds from Aeras and the Bill and Melinda Gates Foundation (JMA & RP-R). RP-R is further a ‘Ramon y Cajal’ fellow from the Spanish Ministry of Economy and Competitiveness, and funded by the Ministry of Economy and Competitiveness SAF2016-77433-R . Tingting Chen and Elise Ishida assisted in the graphic design of Figure 1 .
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/8
Y1 - 2018/8
N2 - A more effective vaccine to control tuberculosis (TB), a major global public health problem, is urgently needed. Current vaccine candidates focus predominantly on eliciting cell-mediated immunity but other arms of the immune system also contribute to protection against TB. We review here recent studies that enhance our current knowledge of antibody-mediated functions against Mycobacterium tuberculosis. These findings, which contribute to the increasing evidence that antibodies have a protective role against TB, include demonstrations that firstly distinct human antibody Fc glycosylation patterns, found in latent M. tuberculosis infection but not in active TB, influence the efficacy of the host to control M. tuberculosis infection, secondly antibody isotype influences human antibody functions, and thirdly that antibodies targeting M. tuberculosis surface antigens are protective. We discuss these findings in the context of TB vaccine development and highlight the need for further research on antibody-mediated immunity in M. tuberculosis infection.
AB - A more effective vaccine to control tuberculosis (TB), a major global public health problem, is urgently needed. Current vaccine candidates focus predominantly on eliciting cell-mediated immunity but other arms of the immune system also contribute to protection against TB. We review here recent studies that enhance our current knowledge of antibody-mediated functions against Mycobacterium tuberculosis. These findings, which contribute to the increasing evidence that antibodies have a protective role against TB, include demonstrations that firstly distinct human antibody Fc glycosylation patterns, found in latent M. tuberculosis infection but not in active TB, influence the efficacy of the host to control M. tuberculosis infection, secondly antibody isotype influences human antibody functions, and thirdly that antibodies targeting M. tuberculosis surface antigens are protective. We discuss these findings in the context of TB vaccine development and highlight the need for further research on antibody-mediated immunity in M. tuberculosis infection.
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U2 - 10.1016/j.coi.2018.04.004
DO - 10.1016/j.coi.2018.04.004
M3 - Review article
C2 - 29656063
AN - SCOPUS:85045376384
SN - 0952-7915
VL - 53
SP - 30
EP - 37
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
ER -