4.7 Article

HIV-1 Transmission During Recent Infection and During Treatment Interruptions as Major Drivers of New Infections in the Swiss HIV Cohort Study

Journal

CLINICAL INFECTIOUS DISEASES
Volume 62, Issue 1, Pages 115-122

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/civ732

Keywords

HIV recent (early) infection; treatment as prevention; treatment interruptions; HIV transmission; endgame

Funding

  1. SHCS - Swiss National Science Foundation [33CS30-148522, 324730-112594, 159868]
  2. SHCS [470, 528, 569, 683]
  3. SHCS Research Foundation
  4. European Community under the Collaborative HIV and Anti-HIV Drug Resistance Network [223131]
  5. Yvonne-Jacob Foundation
  6. Union Bank of Switzerland
  7. Gilead, Switzerland
  8. University of Zurich's Clinical Research Priority Program's ZPHI
  9. University Hospital of Zurich
  10. Swiss National Science Foundation [PZ00P3-142411]

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Background. Reducing the fraction of transmissions during recent human immunodeficiency virus (HIV) infection is essential for the population-level success of treatment as prevention. Methods. A phylogenetic tree was constructed with 19 604 Swiss sequences and 90 994 non-Swiss background sequences. Swiss transmission pairs were identified using 104 combinations of genetic distance (1%-2.5%) and bootstrap (50%-100%) thresholds, to examine the effect of those criteria. Monophyletic pairs were classified as recent or chronic transmission based on the time interval between estimated seroconversion dates. Logistic regression with adjustment for clinical and demographic characteristics was used to identify risk factors associated with transmission during recent or chronic infection. Findings. Seroconversion dates were estimated for 4079 patients on the phylogeny, and comprised between 71 (distance, 1%; bootstrap, 100%) to 378 transmission pairs (distance, 2.5%; bootstrap, 50%). We found that 43.7% (range, 41%-56%) of the transmissions occurred during the first year of infection. Stricter phylogenetic definition of transmission pairs was associated with higher recent-phase transmission fraction. Chronic-phase viral load area under the curve (adjusted odds ratio, 3; 95% confidence interval, 1.64-5.48) and time to antiretroviral therapy (ART) start (adjusted odds ratio 1.4/y; 1.11-1.77) were associated with chronic-phase transmission as opposed to recent transmission. Importantly, at least 14% of the chronic-phase transmission events occurred after the transmitter had interrupted ART. Conclusions. We demonstrate a high fraction of transmission during recent HIV infection but also chronic transmissions after interruption of ART in Switzerland. Both represent key issues for treatment as prevention and underline the importance of early diagnosis and of early and continuous treatment.

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