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. Author manuscript; available in PMC: 2022 Jul 25.
Published in final edited form as: J Acquir Immune Defic Syndr. 2021 Jun 1;87(2):875–881. doi: 10.1097/QAI.0000000000002657

Table 4.

Serostatus to HPV-16 and 18 by competitive Luminex immunoassay (cLIA) and pseudovirion-based immunoassay (PBNA) positivity at baseline among all women and after vaccination

N cLIA*−/PBNA# cLIA+/PBNA+ cLIA+/PBNA− cLIA-/PBNA+
Women in intent-to-treat group at baseline (% seropositive)

HPV-16 DNA-positive 5 1 (20%) 3 (60%) 0 1 (20%)

HPV-16 DNA-negative 111 74 (67%) 21 (19%) 5 (5%) 11 (10%)

HPV-18 DNA-positive 2 1 (50%) 1 (50%) 0 0

HPV-18 DNA-negative 114 85 (75%) 12 (11%) 7 (6%) 10 (9%)


Women in per-protocol group who were DNA negative at baseline (% seropositive)

HPV-16

Baseline
 DNA-negative 102 68 (67%) 19 (19%) 5 (5%) 10 (10%)

Week 28
 DNA-negative 93 0 92 (99%) 0 1 (1%)
 DNA-positive 2 0 2 (100%) 0 0

Week 52
 DNA-negative 97 1 (1%) 95 (98%) 0 1 (1%)
 DNA-positive 0 0 0 0 0

HPV-18

Baseline
 DNA-negative 104 77 (74%) 11 (11%) 7 (7%) 9 (9%)

Week 28
 DNA-negative 96 5 (5%) 88 (92%) 1 (1%) 2 (2%)
 DNA-positive 1 0 1 (100%) 0 0

Week 52
 DNA-negative 97 15 (16%) 69 (71%) 4 (4%) 9 (9%)
 DNA-positive 2 0 0 0 2 (100%)
*

cLIA, competitive Luminex immunoassay (cLIA)

#

PBNA, pseudovirion-based immunoassay (PBNA)