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. Author manuscript; available in PMC: 2020 Aug 5.
Published in final edited form as: J Clin Virol. 2020 Apr 11;127:104344. doi: 10.1016/j.jcv.2020.104344

Table 3:

Results of FDA-approved diagnostic assays a in nine discordant samples from seroconverters (SC) with G4 LAB-plasma Reactive and POC-blood Nonreactive results

Days after first sample collected: RNA: Ag/Ab: IgG/IgM: IgG Suppl:
SC#: APT-Qual Architect Determine GS+O Geenius
Ag Ab
9 10 Pos R NR R R HIV-1 Pos
7 11 Pos R R NR R HIV Neg
11 29 Pos R NR R NR HIV Neg
10 35 Pos R R NR R HIV Neg
4 44 Pos R R R R HIV-1 Ind
14 57 Pos R NR R R HIV-1 Pos
14 71b Pos R NR R R HIV-1 Pos
15 49 Pos R R NR R HIV Neg
15 64b Pos R NR R R HIV-1 Pos
a

Plasma testing: HIV-1 RNA assay: Aptima HIV-1 Qualitative Assay (APT-Qual), Ag/Ab assays: Architect HIV Ag/Ab Combo Assay, Determine HIV-1/2 Ag/Ab Combo, IgG/IgM assay: GS HIV-1/HIV-2 PLUS O EIA (GS+O), IgG supplemental assay (IgG Suppl.): Geenius HIV-1/2 Assay.

b

Samples that became nonreactive in blood after a first POC-reactive test result, potentially due to a second negative diagnostic phase during seroconversion. Sample from SC#14 became nonreactive 12 days after first POC-reactive result, and SC#15 became nonreactive 2 days after first POC-reactive result.