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CD8 T Cell Virus Inhibition Assay Protocol.
Xu, Yinyan; Weideman, Ann Marie; Abad-Fernandez, Maria; Mollan, Katie R; Kallon, Sallay; Samir, Shahryar; Warren, Joanna A; Clutton, Genevieve; Roan, Nadia; Adimora, Adaora A; Archin, Nancie; Kuruc, JoAnn; Gay, Cindy; Hudgens, Michael G; Goonetilleke, Nilu.
Afiliação
  • Xu Y; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Weideman AM; Department of Biostatistics, UNC Chapel Hill, Chapel Hill, North Carolina, USA.
  • Abad-Fernandez M; Center for AIDS Research, School of Medicine, UNC Chapel Hill, Chapel Hill, NC 27599, USA.
  • Mollan KR; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Kallon S; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Samir S; School of Medicine and UNC HIV Cure Center, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Warren JA; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Clutton G; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Roan N; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Adimora AA; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Archin N; Department of Microbiology & Immunology, UNC Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Kuruc J; Department of Urology, University of California San Francisco, CA 94158, USA.
  • Gay C; Gladstone Institute of Virology and Immunology, CA 94158, USA.
  • Hudgens MG; Center for AIDS Research, School of Medicine, UNC Chapel Hill, Chapel Hill, NC 27599, USA.
  • Goonetilleke N; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Bio Protoc ; 12(6): e4354, 2022 Mar 20.
Article em En | MEDLINE | ID: mdl-35434196
The human immunodeficiency virus (HIV)-1 viral inhibition assay (VIA) measures CD8+ T cell-mediated inhibition of HIV replication in CD4+ T cells and is increasingly used for clinical testing of HIV vaccines and immunotherapies. Different VIAs that differ in length of CD8:CD4 T cell culture periods (6-13 days), purity of CD4 cultures [isolated CD4+ T cells or CD8+ depleted peripheral blood mononuclear cells (PBMCs)], HIV strains (laboratory strains, isolates, reporter viruses) and read-outs of virus inhibition (p24 ELISA, intracellular measurement of p24, luciferase reporter expression, and viral gag RNA) have been reported. Here, we describe multiple modifications to a 7-day VIA protocol, the most impactful being the introduction of independent replicate cultures for both HIV infected-CD4 (HIV-CD4) and HIV-CD4:CD8 T cell cultures. Virus inhibition was quantified using a ratio of weighted averages of p24+ cells in replicate cultures and the corresponding 95% confidence intervals. We identify methodological and analysis changes that could be incorporated into other protocols to improve assay reproducibility. We found that in people living with HIV (PLWH) on antiretroviral therapy (ART), CD8 T cell virus inhibition was largely stable over time, supporting the use of this assay and/or analysis methods to examine therapeutic interventions. Graphic abstract.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article