- Pinsent, Amy;
- Solomon, Anthony W;
- Bailey, Robin L;
- Bid, Rhiannon;
- Cama, Anaseini;
- Dean, Deborah;
- Goodhew, Brook;
- Gwyn, Sarah E;
- Jack, Kelvin R;
- Kandel, Ram Prasad;
- Kama, Mike;
- Massae, Patrick;
- Macleod, Colin;
- Mabey, David CW;
- Migchelsen, Stephanie;
- Müller, Andreas;
- Sandi, Frank;
- Sokana, Oliver;
- Taoaba, Raebwebwe;
- Tekeraoi, Rabebe;
- Martin, Diana L;
- White, Michael T
Robust surveillance methods are needed for trachoma control and recrudescence monitoring, but existing methods have limitations. Here, we analyse data from nine trachoma-endemic populations and provide operational thresholds for interpretation of serological data in low-transmission and post-elimination settings. Analyses with sero-catalytic and antibody acquisition models provide insights into transmission history within each population. To accurately estimate sero-conversion rates (SCR) for trachoma in populations with high-seroprevalence in adults, the model accounts for secondary exposure to Chlamydia trachomatis due to urogenital infection. We estimate the population half-life of sero-reversion for anti-Pgp3 antibodies to be 26 (95% credible interval (CrI): 21-34) years. We show SCRs below 0.015 (95% confidence interval (CI): 0.0-0.049) per year correspond to a prevalence of trachomatous inflammation-follicular below 5%, the current threshold for elimination of active trachoma as a public health problem. As global trachoma prevalence declines, we may need cross-sectional serological survey data to inform programmatic decisions.