In-depth Sampling of High-risk Populations to Characterize HIV Transmission Epidemics Among Young MSM Using PrEP in France and Quebec.

HIV MSM PrEP clustering network

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 14 02 2019
accepted: 14 02 2019
entrez: 23 3 2019
pubmed: 23 3 2019
medline: 23 3 2019
Statut: epublish

Résumé

A better understanding of HIV transmission dynamics among populations at high risk is important for development of prevention strategies. We determined HIV transmission networks from infected individuals enrolled in the pre-exposure prophylaxis (PrEP) IPERGAY trial in combination with the ANRS PRIMO and Montreal PHI cohorts to identify and characterize active clusters of transmission in this high-risk population. Genotypic resistance tests were performed on plasma samples from 31 IPERGAY participants. Reverse transcriptase sequences were analyzed in combination with unique HIV Overall, 1893 participants were included. Transmission network analyses revealed that 14 individuals (45.2%) from the IPERGAY trial were involved in 13 clusters sampled over a median period (interquartile range) of 2 (0.3-7.8) years, including 7 dyads and 6 larger clusters ranging from 4 to 28 individuals. When comparing characteristics between clustering individuals enrolled in the PRIMO cohort (n = 377) and in IPERGAY (n = 14), we found that IPERGAY participants had a higher viral load (5.93 vs 5.20 log These results demonstrate high rates of HIV transmission clustering among young high-risk MSM enrolled in the IPERGAY trial. In-depth sampling of high-risk populations may help to uncover unobserved transmission intermediaries and improve prevention efforts that could be targeted to the most active clusters.

Sections du résumé

BACKGROUND BACKGROUND
A better understanding of HIV transmission dynamics among populations at high risk is important for development of prevention strategies. We determined HIV transmission networks from infected individuals enrolled in the pre-exposure prophylaxis (PrEP) IPERGAY trial in combination with the ANRS PRIMO and Montreal PHI cohorts to identify and characterize active clusters of transmission in this high-risk population.
METHODS METHODS
Genotypic resistance tests were performed on plasma samples from 31 IPERGAY participants. Reverse transcriptase sequences were analyzed in combination with unique HIV
RESULTS RESULTS
Overall, 1893 participants were included. Transmission network analyses revealed that 14 individuals (45.2%) from the IPERGAY trial were involved in 13 clusters sampled over a median period (interquartile range) of 2 (0.3-7.8) years, including 7 dyads and 6 larger clusters ranging from 4 to 28 individuals. When comparing characteristics between clustering individuals enrolled in the PRIMO cohort (n = 377) and in IPERGAY (n = 14), we found that IPERGAY participants had a higher viral load (5.93 vs 5.20 log
CONCLUSIONS CONCLUSIONS
These results demonstrate high rates of HIV transmission clustering among young high-risk MSM enrolled in the IPERGAY trial. In-depth sampling of high-risk populations may help to uncover unobserved transmission intermediaries and improve prevention efforts that could be targeted to the most active clusters.

Identifiants

pubmed: 30899768
doi: 10.1093/ofid/ofz080
pii: ofz080
pmc: PMC6422434
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofz080

Subventions

Organisme : NIMH NIH HHS
ID : P30 MH062512
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI131971
Pays : United States

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Auteurs

Antoine Chaillon (A)

Department of Medicine, University of California, San Diego, San Diego, California.

Constance Delaugerre (C)

Virologie, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, CNR VIH, Paris, France.
INSERM U944, CNRS UMR 7212, Institut Universitaire d'Hématologie, Sorbonne Paris Cité, Université Paris Diderot, Hôpital Saint Louis, Paris, France.

Bluma Brenner (B)

BB, Lady Davis Institute, Departments of Medicine, McGill University, Montreal, Canada.

Alix Armero (A)

Virologie, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, CNR VIH, Paris, France.

Catherine Capitant (C)

INSERM SC10 US19, Villejuif, France.

Marie Laure Nere (ML)

Virologie, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, CNR VIH, Paris, France.

Nicolas Leturque (N)

INSERM SC10 US19, Villejuif, France.

Gilles Pialoux (G)

Maladies Infectieuses, Hôpital Tenon, Assistance Publique Hôpitaux de Paris, Paris, France.

Eric Cua (E)

Maladies Infectieuses, Hôpital de l'Archet, Centre Hospitalier de Nice, Nice, France.

Cecile Tremblay (C)

Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

Davey M Smith (DM)

Department of Medicine, University of California, San Diego, San Diego, California.

Cecile Goujard (C)

Assistance Publique Hôpitaux de Paris, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
INSERM CESP U1018, Université Paris Sud, Université Paris Saclay, Saint-Aubin, France.

Laurence Meyer (L)

INSERM SC10 US19, Villejuif, France.
Assistance Publique Hôpitaux de Paris, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
INSERM CESP U1018, Université Paris Sud, Université Paris Saclay, Saint-Aubin, France.

Jean Michel Molina (JM)

INSERM U944, CNRS UMR 7212, Institut Universitaire d'Hématologie, Sorbonne Paris Cité, Université Paris Diderot, Hôpital Saint Louis, Paris, France.
Maladies Infectieuses, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, Paris, France.

Marie Laure Chaix (ML)

Virologie, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, CNR VIH, Paris, France.
INSERM U944, CNRS UMR 7212, Institut Universitaire d'Hématologie, Sorbonne Paris Cité, Université Paris Diderot, Hôpital Saint Louis, Paris, France.

Classifications MeSH