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. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2020 May 1;84(1):85–91. doi: 10.1097/QAI.0000000000002299

TABLE 2.

Individual Biomarkers of Imbalanced Immunity Associated With HIV Acquisition Risk

Population
A
B
Biomarker of Imbalanced Immunity
OR (95% CI)
OR (95% CI)
Cervical (Mucosal) 4390 Visits (574 From Seroconverters) 3007 Visits (200 From Seroconverters)
High concentrations of (>median) primary pro-inflammatory cytokines
 IL-1β 1.00 (0.84 to 1.19) 1.26 (0.94 to 1.68)
 IL-6 1.07 (0.90 to 1.28) 1.07 (0.80 to 1.43)
Low concentrations of (<median) anti-inflammatory function
 IL-1RA 0.98 (0.82 to 1.16) 0.65 (0.48 to 0.86)**
 SLPI 1.16 (0.98 to 1.39) 1.11 (0.83 to 1.48)
 IL-1RA: IL-1β ratio 0.97 (0.81 to 1.16) 0.72 (0.54 to 0.96)*
High concentrations of (>median) secondary immune effectors
 IL-8 1.18 (0.99 to 1.41) 0.86 (0.64 to 1.14)
 MIP-3α 0.86 (0.72 to 1.02) 0.92 (0.69 to 1.22)
 RANTES 1.20 (1.01 to 1.43)* 1.58 (1.17 to 2.12)**
 BD2 1.33 (1.11 to 1.58)** 1.60 (1.19 to 2.14)**
Low concentrations of (<median) anti-viral stress response
 ICAM-1 1.06 (0.89 to 1.26) 0.92 (0.69 to 1.23)
 VEGF 0.90 (0.76 to 1.07) 0.80 (0.60 to 1.07)

Population
A
B
Biomarker of Imbalanced Immunity
OR (95% CI)
OR (95% CI)
Serum (Systemic) 2636 Visits (445 From Seroconverters) 1498 Visits (154 From Seroconverters)

Low concentrations of (<median) systemic immunity
 CRP 1.49 (1.21 to 1.83)*** 1.45 (1.04 to 2.04)*
 IL-6 1.23 (1.00 to 1.51)* 0.95 (0.68 to 1.33)
 IL-7 1.15 (0.94 to 1.41) 0.92 (0.66 to 1.28)
High concentrations of (middle quartile) response to endotoxin exposure
 sCD14 1.03 (0.81 to 1.30) 1.00 (0.66 to 1.51)

Bivariate analysis was used to calculate odds ratios (OR) and 95% confidence intervals (CI) of having high concentrations of or low concentrations of mediators of mucosal and systemic immunity in cervical and serum specimens from women who seroconverted compared to controls who remained HIV-negative.

*

P < 0.05

**

P < 0.01

***

P < 0.001.

Population A includes all data for both seroconverters and women remaining HIV-negative from all HIV-negative visits. Population B includes all HIV-negative visits from women remaining HIV-negative but limited data for the seroconverters to the visit just before the seroconversion visit.