Skip to main content
. 2012 Jul 16;13(4):669–671. doi: 10.2450/2015.0034-15

Table I.

Summary of the HIV serology and NAT results for the index donation and four subsequent follow-up samples from the case study donor. Results are included for testing at both the Australian Red Cross Blood Service (Blood Service) and the Victorian Infectious Diseases Reference Laboratory (VIDRL).

Date Blood Service results Victorian Infectious Diseases Reference Laboratory (VIDRL) results
Serology NAT Murex 1.2 O HIV EIA Western blot5 Abbott Real Time Roche6

Prism HIV O Plus s/co ratios1 Genscreen HIV Ultra s/co ratios2 Ultrio3 dHIV4
17/03/12 (index donation) 60.9
69.0, 67.2
7.5, 7.5 NR NT REA p24++, gp160++ ND NT

12/04/12 77.5
65.8, 65.5
11.7, 11.7 NR NR REA p24++, gp 120+, gp160++ NT ND

10/05/12 65.5
66.4, 66.7
13.0, 13.1 NT REA REA p24++, gp 120+, gp160++ ND NT

12/06/12 61.1
70.3, 65.3
13.2, 13.2 NR NR REA p24++, gp 120+, gp160++ NT ND7

21/06/12 70.3
83.3, 71.1
13.1, 12.2 NR REA8 NT NT NT ND9
1

s/co ratio: sample to cutoff ratio; s/co ratio ≥1.0 = REA; s/co ratios for initial test and duplicate repeat tests;

2

s/co ratio: sample to cutoff ratio; s/co ratio ≥1.0 = REA; samples tested in duplicate;

3

Ultrio: Procleix Ultrio multiplex assay;

4

dHIV: Procleix HIV-1 discriminatory assay;

5

MP Diagnostics HIV Blot 2.2;

6

Roche Ampliprep/Taqman HIV-1 Test version 2.0;

7

six of six replicates were non-reactive;

8

two of 20 replicates were reactive;

9

nine of nine replicates were non-reactive.

NAT: nucleic acid testing; HIV: human immunodeficiency virus; NR: non-reactive; NT: not tested; REA: reactive; ND: not detected.