Evidence map›Paper›PMID 32843050›Full record

ArticleAntimicrobial resistance and infection control2020

First case of Dolutegravir and Darunavir/r multi drug-resistant HIV-1 in Cameroon following exposure to Raltegravir: lessons and implications in the era of transition to Dolutegravir-based regimens.

Joseph Fokam, Desire Takou, Ezechiel Ngoufack Jagni Semengue, Georges Teto, Grace Beloumou, Beatrice Dambaya, Maria-Mercedes Santoro, Leonella Mossiang, Serge Clotaire Billong, Fatim Cham and 15 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Antimicrobial resistance and infection control, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 3 countries.

Joseph FokamChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon. fokamjoseph@circb.cm.ORCID 0000-0002-1501-2763
Desire TakouChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Ezechiel Ngoufack Jagni SemengueChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Georges TetoChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Grace BeloumouChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Beatrice DambayaChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Maria-Mercedes SantoroUniversity of Rome Tor Vergata, Rome, Italy.
Leonella MossiangHIV Treatment Centre, Yaoundé Central Hospital, Yaoundé, Cameroon.
Serge Clotaire BillongFaculty of Health Sciences, University of Buea, Buea, Cameroon.
Fatim ChamWorld Health Organisation, Regional Office for Africa (AFRO), Brazzaville, Congo.
Samuel Martin SossoChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Edith Saounde TemgouaCentral Technical Group, National AIDS Control Committee, Yaoundé, Cameroon.
Aubin Joseph NanfackChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Sylvie MoudourouChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Nelly KamgaingChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Rachel KamgaingChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Joelle Nounouce Ngako PamenFaculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Mireille Mpoudi Ngole EtameHIV Treatment Centre, Military Hospital, Yaoundé, Cameroon.
Anne-Cecile Z-K BissekFaculty of Health Sciences, University of Buea, Buea, Cameroon.
Jean-Bosco N ElatFaculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Emmanuel Eben MoussiChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Vittorio ColizziChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Carlo-Federico PernoChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
Alexis NdjoloChantal BIYA International Reference Centre for research on HIV/AIDS prevention and management, Yaoundé, Cameroon.
VIROFORUM
Centre International De Reference Chantal Biya · CMUniversité de Yaoundé I · CMUniversity of Rome Tor Vergata · ITCentral Hospital of Yaoundé · CMNational Radiation Protection Agency of Cameroon · CMWorld Health Organization Regional Office for Africa · CG

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundSub-Saharan African countries are transitioning to dolutegravir-based regimens, even for patients with extensive previous drug exposure, including first-generation integrase strand-transfer inhibitors (INSTI) such as raltegravir. Such exposure might have implications on cross-resistance to dolutegravir-based antiretroviral therapies (ART). CASE PRESENTATION: We report a 65 years old Cameroonian, previously exposed to raltegravir, and failing on third-line treatment with multi-drug resistance to darunavir/r and dolutegravir. Genotypic resistance testing (GRT) and viral tropism were performed during monitoring time points. The patient initiated ART in August 2007. At the time point of the first (29.04.2010), second (01.12.2017) and third (08.08.2019) GRT, prior ART exposure included 3TC, d4T, NVP and EFV; additionally TDF, DRV/r and RAL; and additionally ABC and DTG respectively. First GRT revealed mutations associated with resistance only to first-generation Non-nucleoside reverse transcriptase inhibitors (NNRTI). Second GRT revealed mutations associated with high-level resistance to all NRTIs, first generation NNRTIs, all ritonavir boosted protease inhibitors (PI/r), and all INSTI, while viral tropism (using geno2pheno) revealed a CCR5-tropic virus with a false positive rate (FPR) of 60.9% suggesting effectiveness of maraviroc (MRV). The third GRT showed high-level resistance to NRTI, NNRTI, all PI and all INSTI, with additional mutations (H221HY for NNRTI and S147G for INSTI), and a CCR5-tropic virus with a slightly reduced FPR (57.0%). Without any locally available active therapeutic option, the patient has been on a maintenance therapy with "DRV/r (600mg x 2/day)+TDF+3TC" and patient/family-centered adherence has been reinforced. Since the first viral load (VL) measurement in 2010, the patient has had 12 VL tests with the VL ranging from 4.97 Log to 6.44 Log copies/mL and the CD4 count never exceeded 200 cells/μL.

conclusionsAs African countries transition to dolutegravir-based regimens, prior raltegravir-exposure may prompt selection (and potential transmission) of dolutegravir-resistance, supporting case surveillance.

Indexed as

Drug Resistance, Multiple, ViralAgedAnti-HIV AgentsCameroonCD4 Lymphocyte CountDarunavirDolutegravirHeterocyclic Compounds, 3-RingHIV-1HIV InfectionsHumansMaleOxazinesPiperazinesPyridonesRaltegravir PotassiumAnti-HIV AgentsDarunavirDolutegravirHeterocyclic Compounds, 3-RingOxazinesPiperazinesPyridonesRaltegravir PotassiumCameroonHIV drug resistanceIntegrase inhibitorsProtease inhibitorsViral tropism

Identifiers

PMID32843050
PMCPMC7449072
OpenAlexW3081112286

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.