Past, present and future directions in human genetic susceptibility to tuberculosis. Möller, M., de Wit, E., & Hoal, E. G. FEMS immunology and medical microbiology, 58(1):3–26, February, 2010. 00090 doi abstract bibtex The historical impression that tuberculosis was an inherited disorder has come full circle and substantial evidence now exists of the human genetic contribution to susceptibility to tuberculosis. This evidence has come from several whole-genome linkage scans, and numerous case-control association studies where the candidate genes were derived from the genome screens, animal models and hypotheses pertaining to the disease pathways. Although many of the associated genes have not been validated in all studies, the list of those that have been is growing, and includes NRAMP1, IFNG, NOS2A, MBL, VDR and some TLR. Certain of these genes have consistently been associated with tuberculosis in diverse populations. The future investigation of susceptibility to tuberculosis is almost certain to include genome-wide association studies, admixture mapping and the search for rare variants and epigenetic mechanisms. The genetic identification of more vulnerable individuals is expected to inform personalized treatment and perhaps vaccination strategies.
@article{moller_past_2010,
title = {Past, present and future directions in human genetic susceptibility to tuberculosis},
volume = {58},
issn = {1574-695X},
doi = {10.1111/j.1574-695X.2009.00600.x},
abstract = {The historical impression that tuberculosis was an inherited disorder has come full circle and substantial evidence now exists of the human genetic contribution to susceptibility to tuberculosis. This evidence has come from several whole-genome linkage scans, and numerous case-control association studies where the candidate genes were derived from the genome screens, animal models and hypotheses pertaining to the disease pathways. Although many of the associated genes have not been validated in all studies, the list of those that have been is growing, and includes NRAMP1, IFNG, NOS2A, MBL, VDR and some TLR. Certain of these genes have consistently been associated with tuberculosis in diverse populations. The future investigation of susceptibility to tuberculosis is almost certain to include genome-wide association studies, admixture mapping and the search for rare variants and epigenetic mechanisms. The genetic identification of more vulnerable individuals is expected to inform personalized treatment and perhaps vaccination strategies.},
language = {eng},
number = {1},
journal = {FEMS immunology and medical microbiology},
author = {Möller, Marlo and de Wit, Erika and Hoal, Eileen G.},
month = feb,
year = {2010},
pmid = {19780822},
note = {00090 },
keywords = {Animals, Bacterial Proteins, Case-Control Studies, Genetic Predisposition to Disease, Genome-Wide Association Study, Guinea Pigs, Humans, Mice, Mycobacterium tuberculosis, Rabbits, Tuberculosis},
pages = {3--26},
}
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