Barely Significant

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In contrast to the healthy controls who showed a trend of age-dependent Treg cell subpopulations ( Figure 4A ) ( 52 , 53 ), the majority of the studied PIDs patients had a more age-independent predicted Treg cell subpopulation ( Figure 4C ), but over 85% (78/91) maintained relatively lower Th17 populations that inhibited human B cell survival and activation of antibody-secreting plasma cells ( 54 ).
The authors showed a trend toward lower baseline Tregs and M-MDSC levels in non-relapsing patients as compared with relapsing ones, thus suggesting the negative impact of these circulating populations on the clinical outcome, without clearly distinguishing their predictive vs. prognostic value ( 51 ).