What do the Universal Test and Treat trials tell us about the path to HIV epidemic control?


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
02 2020
Historique:
received: 17 10 2019
accepted: 14 01 2020
entrez: 25 2 2020
pubmed: 25 2 2020
medline: 5 11 2020
Statut: ppublish

Résumé

Achieving HIV epidemic control globally will require new strategies to accelerate reductions in HIV incidence and mortality. Universal test and treat (UTT) was evaluated in four randomized population-based trials (BCPP/Ya Tsie, HPTN 071/PopART, SEARCH, ANRS 12249/TasP) conducted in sub-Saharan Africa (SSA) during expanded antiretroviral treatment (ART) eligibility by World Health Organization guidelines and the UNAIDS 90-90-90 campaign. These three-year studies were conducted in Botswana, Zambia, Uganda, Kenya and South Africa in settings with baseline HIV prevalence from 4% to 30%. Key observations across studies were: (1) Universal testing (implemented via a variety of home and community-based testing approaches) achieved >90% coverage in all studies. (2) When coupled with robust linkage to HIV care, rapid ART start and patient-centred care, UTT achieved among the highest reported population levels of viral suppression in SSA. Significant gains in population-level viral suppression were made in regions with both low and high baseline population viral load; however, viral suppression gains were not uniform across all sub-populations and were lower among youth. (3) UTT resulted in marked reductions in community HIV incidence when universal testing and robust linkage were present. However, HIV elimination targets were not reached. In BCPP and HPTN 071, annualized HIV incidence was approximately 20% to 30% lower in the intervention (which included universal testing) compared to control arms (no universal testing). In SEARCH (where both arms had universal testing), incidence declined 32% over three years. (4) UTT reduced HIV associated mortality by 23% in the intervention versus control communities in SEARCH, a study in which mortality was comprehensively measured. These trials provide strong evidence that UTT inclusive of universal testing increases population-level viral suppression and decreases HIV incidence and mortality faster than the status quo in SSA and should be adapted at a sub-country level as a public health strategy. However, more is needed, including integration of new prevention interventions into UTT, in order to reach UNAIDS HIV elimination targets.

Identifiants

pubmed: 32091179
doi: 10.1002/jia2.25455
pmc: PMC7038879
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25455

Subventions

Organisme : Medical Research Council
ID : MR/R010161/1
Pays : United Kingdom
Organisme : CGH CDC HHS
ID : U01 GH000447
Pays : United States
Organisme : CGH CDC HHS
ID : U2G GH001911
Pays : United States
Organisme : PEPFAR
Pays : United States

Informations de copyright

© 2020 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Diane Havlir (D)

Department of Medicine, University of California San Francisco, San Francisco, CA, USA.

Shahin Lockman (S)

Brigham and Women's Hospital, Boston, MA, USA.
Harvard School T.H. Chan School of Public Health, Boston, MA, USA.
Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Helen Ayles (H)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Zambart, Lusaka, Zambia.

Joseph Larmarange (J)

Centre Population et Développement, Institut de Recherche pour le Développement, Université Paris Descartes, Inserm, Paris, France.
Africa Health Research Institute, Somkhele, South Africa.

Gabriel Chamie (G)

Department of Medicine, University of California San Francisco, San Francisco, CA, USA.

Tendani Gaolathe (T)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
University of Botswana, Gaborone, Botswana.

Collins Iwuji (C)

Department of Global Health & Infection, Brighton and Sussex Medical School, Brighton, United Kingdom.
Africa Health Research Institute, KwaZulu-Natal, South Africa.
Research Department of Infection and Population Health, University College London, London, United Kingdom.

Sarah Fidler (S)

Imperial College, National Institute for Health Research Biomedical Research Center, London, United Kingdom.
Department of Infectious Disease, Imperial College London, London, United Kingdom.

Moses Kamya (M)

Department of Medicine, Makerere University, Kampala, Uganda.
Infectious Diseases Research Collaboration (IDRC), Kampala, Uganda.

Sian Floyd (S)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Janet Moore (J)

Division of Global HIV/AIDS and TB, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Richard Hayes (R)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Maya Petersen (M)

School of Public Health, University of California Berkeley, Berkeley, CA, USA.

Francois Dabis (F)

ISPED & Inserm Bordeaux Population Health UMR 1219, Univ Bordeaux, Bordeaux, France.

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