Review Article

Efficacy and Safety of Adjunctive Recombinant Human Interleukin-2 for Patients with Pulmonary Tuberculosis: A Meta-Analysis

Table 3

Univariate meta-regression analyses for the association between patient and treatment characteristics with the efficacy outcomes.

RR for sputum culture conversion to negative
CovariateCoefficient95% CI
No. of patients0.047−0.148 to 0.2420.67
Mean age (years)−0.032−0.099 to 0.0350.59
rhuIL-2 dose (104 IU/d)0.0027−0.0011 to 0.00650.18
rhuIL-2 routes−0.06−0.17 to 0.050.29
Treatment duration (months)0.18−0.22 to 0.580.49

RR for sputum smear conversion to negative
CovariateCoefficient95% CI
No. of patients0.19−0.04 to 0.420.11
Mean age (years)0.009−0.017 to 0.0350.63
rhuIL-2 dose (104 U/d)−0.013−0.251 to 0.2250.92
rhuIL-2 routes−0.31−0.97 to 0.350.36
Treatment duration (months)0.33−0.10 to 0.760.18

RR for radiographic focus absorption
CovariateCoefficient95% CI
No. of patients0.03−0.19 to 0.250.85
Mean age (years)−0.044−0.102 to 0.0140.13
rhuIL-2 dose (104 IU/d)−0.052−0.153 to 0.0490.36
rhuIL-2 routes−0.063−0.272 to 0.1460.64
Treatment duration (months)0.14−0.58 to 0.860.77

RR for radiographic cavity closure
CovariateCoefficient95% CI
No. of patients−0.012−0.511 to 0.4870.93
Mean age (years)0.091−0.072 to 0.2540.10
rhuIL-2 dose (104 IU/d)0.058−0.122 to 0.2380.52
rhuIL-2 routes−0.015−0.523 to 0.4930.96
Treatment duration (months)−0.072−0.301 to 0.1570.61

rhuIL-2, recombinant human interleukin-2; RR, risk ratio; CI, confidence interval.