Protection by BCG vaccine against tuberculosis: a systematic review of randomized controlled trials
- PMID: 24336911
- DOI: 10.1093/cid/cit790
Protection by BCG vaccine against tuberculosis: a systematic review of randomized controlled trials
Abstract
Background: Randomized trials assessing BCG vaccine protection against tuberculosis have widely varying results, for reasons that are not well understood.
Methods: We examined associations of trial setting and design with BCG efficacy against pulmonary and miliary or meningeal tuberculosis by conducting a systematic review, meta-analyses, and meta-regression.
Results: We identified 18 trials reporting pulmonary tuberculosis and 6 reporting miliary or meningeal tuberculosis. Univariable meta-regression indicated efficacy against pulmonary tuberculosis varied according to 3 characteristics. Protection appeared greatest in children stringently tuberculin tested, to try to exclude prior infection with Mycobacterium tuberculosis or sensitization to environmental mycobacteria (rate ratio [RR], 0.26; 95% confidence interval [CI], .18-.37), or infants (RR, 0.41; 95% CI, .29-.58). Protection was weaker in children not stringently tested (RR, 0.59; 95% CI, .35-1.01) and older individuals stringently or not stringently tested (RR, 0.88; 95% CI, .59-1.31 and RR, 0.81; 95% CI, .55-1.22, respectively). Protection was higher in trials further from the equator where environmental mycobacteria are less and with lower risk of diagnostic detection bias. These associations were attenuated in a multivariable model, but each had an independent effect. There was no evidence that efficacy was associated with BCG strain. Protection against meningeal and miliary tuberculosis was also high in infants (RR, 0.1; 95% CI, .01-.77) and children stringently tuberculin tested (RR, 0.08; 95% CI, .03-.25).
Conclusions: Absence of prior M. tuberculosis infection or sensitization with environmental mycobacteria is associated with higher efficacy of BCG against pulmonary tuberculosis and possibly against miliary and meningeal tuberculosis. Evaluations of new tuberculosis vaccines should account for the possibility that prior infection may mask or block their effects.
Keywords: BCG vaccine; meta-analysis; meta-regression; trials; vaccine efficacy.
Comment in
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Understanding BCG is the key to improving it.Clin Infect Dis. 2014 Feb;58(4):481-2. doi: 10.1093/cid/cit793. Epub 2013 Dec 13. Clin Infect Dis. 2014. PMID: 24336910 Free PMC article. No abstract available.
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BCG, Latitude, and Environmental Mycobacteria.Clin Infect Dis. 2014 Aug 15;59(4):607-8. doi: 10.1093/cid/ciu331. Epub 2014 May 6. Clin Infect Dis. 2014. PMID: 24803373 No abstract available.
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Problems with ascribing between-trial differences in BCG effectiveness to sensitization with environmental mycobacteria.Clin Infect Dis. 2014 Aug 15;59(4):605-7. doi: 10.1093/cid/ciu329. Epub 2014 May 6. Clin Infect Dis. 2014. PMID: 24803374 No abstract available.
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Reply to Kernodle and von Reyn.Clin Infect Dis. 2014 Aug 15;59(4):608-9. doi: 10.1093/cid/ciu330. Epub 2014 May 6. Clin Infect Dis. 2014. PMID: 24803378 No abstract available.
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