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. 2005 Nov;79(22):13882–13891. doi: 10.1128/JVI.79.22.13882-13891.2005

TABLE 2.

Detection by ELISA of anti-VP4 antibodies in plasma from healthy subjects and patients with IDDM

Subject group (n) Anti-VP4CVB3
Anti-VP4CVB4
No. (%) with positive detectiona Index valueb No. (%) with positive detectiona Index valueb
Healthy subjects 40 14 (35) 0.9 ± 0.32 6 (15) 0.72 ± 0.34
IDDM patients 40 25 (62.5)c 1.88 ± 1.09d 32 (80)e 1.96 ± 0.85d
a

Number of individuals with positive antibody detection by ELISA.

b

Index values of anti-VP4 antibodies detected by ELISA. Microtiter plates were coated with VP4 dissociated from either CVB3 or CVB4 (CVB4E2). In the same way, microtiter plates were coated with proteins obtained from a mock dissociation procedure. The immunoassay cutoff value was determined by adding the specimen absorbance on mock infection plates to the blank absorbance on VP4 plates. The index value is obtained by calculating the specimen/cutoff value ratio. Data are presented as means ± standard deviations.

c

P < 0.02 versus healthy subjects (χ2 test).

d

P < 0.001 versus healthy subjects (Student's t test).

e

P < 0.001 versus healthy subjects (χ2 test).