Immunogenicity assessment of HPV16/18 vaccine using the glutathione S-transferase L1 multiplex serology assay

Hum Vaccin Immunother. 2014;10(10):2965-74. doi: 10.4161/21645515.2014.972811.

Abstract

The glutathione S-transferase (GST)-L1 multiplex serology assay has favorable properties for use in clinical trials and epidemiologic studies, including low cost, high throughput capacity, and low serum volume requirement. Therefore, we evaluated the GST-L1 assay as a measure of HPV16/18 vaccine immunogenicity. Our study population included 65 women selected from the Costa Rica Vaccine Trial who received the bivalent HPV16/18 virus-like particle (VLP) vaccine at the recommended 0/1/6-month schedule. We tested replicate serum samples from months 0/1/12 (i.e., after 0/1/3 doses) by GST-L1 and 3 other commonly used serology assays, VLP-ELISA, SEAP-NA, and cLIA. We calculated the percentage of women seropositive by GST-L1 by time point and HPV type (14 HPV types), and compared GST-L1 to other assays using Spearman rank correlation coefficients. After 1 vaccine dose, seropositivity by GST-L1 was 40% each for HPV16 and HPV18, increasing to 100% and 98%, respectively, after 3 doses. Seropositivity after 3 doses ranged from 32% to 69% for HPV types 31/33/45, for which partial vaccine efficacy is reported, though increases also occurred for types with no evidence for cross-protection (e.g., HPV77). GST-L1 correlated best after 3 doses with VLP-ELISA (HPV16 and HPV18 each ρ = 0.72) and SEAP-NA (HPV16 ρ = 0.65, HPV18 ρ = 0.71) (all P < 0.001); correlation was lower with cLIA. The GST-L1 is suitable for evaluating HPV16/18 vaccine immunogenicity after 3 vaccine doses, although in contrast to other assays it may classify some samples as HPV16/18 seronegative. The assay's utility is limited for lower antibody levels such as after receipt of 1 dose.

Keywords: BKV, BK virus; CV, coefficient of variation; CVT, Costa Rica Vaccine Trial; EU/mL, ELISA units per milliliter; GST-L1 multiplex serology; GST-L1, glutathione S-transferase L1 multiplex serology assay; HPV vaccine; HPV, human papillomavirus; ICC, intraclass correlation coefficient; JCV, JC virus; LLOD, lower limit of detection; MFI, median fluorescence units; OD, optical density; SEAP-NA; SEAP-NA, secreted alkaline phosphatase neutralization assay; VLP, virus-like particle; VLP-ELISA; VLP-ELISA, virus-like particle-based enzyme linked immunosorbent assay; cLIA; cLIA, competitive Luminex immunoassay; human papillomavirus (HPV); immunogenicity assessment; mMU/mL, milli-Merck units per milliliter.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neutralizing / blood
  • Antibodies, Neutralizing / immunology
  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology
  • Antibody Formation / immunology
  • Biological Assay / methods*
  • Costa Rica
  • Cross Protection
  • Female
  • Glutathione Transferase / metabolism
  • Human papillomavirus 16 / immunology*
  • Human papillomavirus 18 / immunology*
  • Humans
  • Immunization, Secondary
  • Papillomavirus Infections / immunology*
  • Papillomavirus Infections / prevention & control
  • Papillomavirus Vaccines / immunology*
  • Reproducibility of Results
  • Vaccination

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Papillomavirus Vaccines
  • Glutathione Transferase