Literature DB >> 17587535

Quinoline compounds decrease in vitro spontaneous proliferation of peripheral blood mononuclear cells (PBMC) from human T-cell lymphotropic virus (HTLV) type-1-infected patients.

Fernanda Grassi1, Ana Beatriz Guimarães Corrêa, Rita Elizabeth Mascarenhas, Bernardo Galvão, Blandine Séon-Méniel, Fanny Schmidt, Xavier Franck, Reynald Hocquemiller, Bruno Figadère, Alain Fournet.   

Abstract

In vitro spontaneous proliferation is the immunological hallmark of peripheral blood mononuclear cells (PBMC) from HTLV-1-infected individuals. Quinoline compounds down regulate in vitro cell proliferation of HTLV-1 transformed cell lines. In the present study we assessed the capacity of quinolines to inhibit spontaneous cell proliferation of PBMC from HTLV-1-infected individuals. Twenty-two quinolines were evaluated. Toxicity was first assessed on PBMC from healthy donors by using both the Trypan blue technique and Tetrazolium Salt (XTT) method and then the antiproliferative effect was measured by a classic lymphoproliferative assay on PBMC from three HTLV-1-infected individuals, in the presence of decreasing concentrations of quinolines (from 100microM to 0.8microM), after 5 days of culture. We found that 14 out of 22 compounds were non-toxic to PBMC from uninfected individuals at 100, 50 and 10microM. Four compounds presented a capacity to inhibit more than 80% of the spontaneous proliferation: 7 at 25microM and 10, 20 and 23 at 100microM. Our results indicate that some quinolines block spontaneous proliferation of PBMC from HTLV-1-infected individuals.

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Year:  2007        PMID: 17587535     DOI: 10.1016/j.biopha.2007.05.003

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  3 in total

1.  Inhibition of in vitro Ebola infection by anti-parasitic quinoline derivatives.

Authors:  Shawn Goyal; Beth Binnington; Stephen D S McCarthy; Didier Desmaële; Laurent Férrié; Bruno Figadère; Philippe M Loiseau; Donald R Branch
Journal:  F1000Res       Date:  2020-04-17

2.  Inhibition of Chikungunya Virus Infection by 4-Hydroxy-1-Methyl-3-(3-morpholinopropanoyl)quinoline-2(1H)-one (QVIR) Targeting nsP2 and E2 Proteins.

Authors:  Mohammad Islamuddin; Obaid Afzal; Wajihul Hasan Khan; Malik Hisamuddin; Abdulmalik Saleh Alfawaz Altamimi; Ibraheem Husain; Kentaro Kato; Mubarak A Alamri; Shama Parveen
Journal:  ACS Omega       Date:  2021-03-31

Review 3.  The Potential of 2-Substituted Quinolines as Antileishmanial Drug Candidates.

Authors:  Philippe M Loiseau; Kaluvu Balaraman; Gillian Barratt; Sébastien Pomel; Rémy Durand; Frédéric Frézard; Bruno Figadère
Journal:  Molecules       Date:  2022-04-02       Impact factor: 4.411

  3 in total

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