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. Author manuscript; available in PMC: 2024 Jun 13.
Published in final edited form as: J Clin Virol. 2017 Mar 23;91:90–94. doi: 10.1016/j.jcv.2017.03.012

Table 4.

Comparison of INSTI performance with discrepant results in simulated whole blood and plasma from four HIV-1 seroconverters with other assays during positive and negative time points

Sample Days between bleeds NAT IA IA RT INSTI

Ag/Ab IgG/IgM Ag Ab plasma whole blood

924-04 nonreactive +
924-05 16 reactive + +
924-06 7 reactive + + + + + +
924-07 2 reactive + + + + +
924-08 5 reactive + + + + +

931-05 reactive + +
931-06 13 reactive + + + + + +
931-07 5 reactive + + + + +
931-08 2 reactive + + + + +
931-09 7 reactive + + + + +

940-01 reactive +
940-02 7 reactive + + +
940-03 4 reactive + + + + + +
940-04 4 reactive + + + + +
940-05 3 reactive + + + + +

944-01 reactive
944-02 2 reactive
944-03 5 reactive + + +
944-04 2 reactive + + +
944-05 5 nonreactive + + + + +
944-06 2 reactive + + + + +

NAT: FDA-approved diagnostic nucleic acid test; IA Ag/Ab: FDA-approved laboratory-based antigen/antibody immunoassay; IA IgG/IgM: FDA-approved laboratory-based IgG/IgM immunoassay; RT Ag/Ab: FDA-approved antigen/antibody rapid test