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. 2008 Feb;151(2):260–266. doi: 10.1111/j.1365-2249.2007.03561.x

Table 2.

Serum YKL-40 and markers of the immune risk phenotype.

Low YKL-40 Medium YKL-40 High YKL-40
CD4 : CD8 ratio 2·3 (1·5–3·4) 2·7 (1·8–3·5) 1·7 (1·3–2·3)*
n = 50 n = 49 n = 47
CD28CD8+ (cells/ml blood) 135 (81–192) × 103 115 (60–160) × 103 154 (71–263) × 103
n = 43 n = 43 n = 41
PHA proliferation (cpm) 8392 (5161–11 078) 7764 (5811–9003) 7457 (5408–9542)
n = 48 n = 47 n = 48
PWM proliferation (cpm) 1275 (884–2174) 1158 (651–1823) 1255 (764–2430)
n = 47 n = 47 n = 47
IL-2 proliferation (cpm) 644 (307–890) 518 (320–960) 572 (392–860)
n = 47 n = 45 n = 44
NK (cells/ml blood) 183 (104–317) × 103 159 (96–284) × 103 182 (97–281) × 103
n = 44 n = 44 n = 39
NK cytotoxicity (%) 10 (6–17) 15 (8–21) 12 (9–24)
n = 46 n = 50 n = 45
*

Denotes P < 0·02 in a one-way analysis of variance. Turkey post-hoc test shows significant difference between medium YKL-40 and high YKL-40. Natural killer (NK) cell cytotoxicity has the effector/target cell ratio 50 : 1. YKL-40 is divided by tertiles into low, medium and high. Median and quartiles are shown. The immune risk phenotype constitutes a predictor of non-survival in longitudinal studies. PHA, phytohaemagglutinin; PWM, pokeweed mitogen; IL-2, interleukin-2; cpm: counts per million.