Mycobacterium tuberculosis infection, immune activation, and risk of HIV acquisition.

Although aORs differed by LTBI status, as RISK6 was associated with lower HIV risk in those with LTBI and showed a trend towards increased HIV risk in those without LTBI, we could not rule out that this difference was due to chance.

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Therefore, given that there are only two primary hypotheses tested (LTBI or RISK6 association with HIV risk), we are no longer presenting unadjusted p values for the flow analyses in Table 2, which includes only 3 tests (1 primary and 2 secondary), with no change in inference with either strategy (none approached significance with nominal p-values).

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