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Immune correlates of the Thai RV144 HIV vaccine regimen in South Africa.
Gray, Glenda E; Huang, Ying; Grunenberg, Nicole; Laher, Fatima; Roux, Surita; Andersen-Nissen, Erica; De Rosa, Stephen C; Flach, Britta; Randhawa, April K; Jensen, Ryan; Swann, Edith M; Bekker, Linda-Gail; Innes, Craig; Lazarus, Erica; Morris, Lynn; Mkhize, Nonhlanhla N; Ferrari, Guido; Montefiori, David C; Shen, Xiaoying; Sawant, Sheetal; Yates, Nicole; Hural, John; Isaacs, Abby; Phogat, Sanjay; DiazGranados, Carlos A; Lee, Carter; Sinangil, Faruk; Michael, Nelson L; Robb, Merlin L; Kublin, James G; Gilbert, Peter B; McElrath, M Juliana; Tomaras, Georgia D; Corey, Lawrence.
Afiliación
  • Gray GE; Perinatal HIV Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 1864, South Africa. glenda.gray@mrc.ac.za.
  • Huang Y; South African Medical Research Council, Cape Town 7505, South Africa.
  • Grunenberg N; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Laher F; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Roux S; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Andersen-Nissen E; Perinatal HIV Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 1864, South Africa.
  • De Rosa SC; The Desmond Tutu HIV Centre, University of Cape Town, Cape Town 8001, South Africa.
  • Flach B; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Randhawa AK; Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town 8001, South Africa.
  • Jensen R; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Swann EM; Cape Town HVTN Immunology Laboratory, Hutchinson Centre Research Institute of South Africa, Cape Town 8001, South Africa.
  • Bekker LG; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Innes C; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Lazarus E; Vaccine Research Program, Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20852, USA.
  • Morris L; The Desmond Tutu HIV Centre, University of Cape Town, Cape Town 8001, South Africa.
  • Mkhize NN; The Aurum Institute, Klerksdorp 2570, South Africa.
  • Ferrari G; Perinatal HIV Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 1864, South Africa.
  • Montefiori DC; National Institute for Communicable Diseases, National Health Laboratory Service, Sandringham, Johannesburg 2192, South Africa.
  • Shen X; National Institute for Communicable Diseases, National Health Laboratory Service, Sandringham, Johannesburg 2192, South Africa.
  • Sawant S; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
  • Yates N; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
  • Hural J; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
  • Isaacs A; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
  • Phogat S; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
  • DiazGranados CA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Lee C; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Sinangil F; Sanofi Pasteur, Swiftwater, PA 18370, USA.
  • Michael NL; Sanofi Pasteur, Swiftwater, PA 18370, USA.
  • Robb ML; Global Solutions for Infectious Diseases, South San Francisco, CA 94080, USA.
  • Kublin JG; Global Solutions for Infectious Diseases, South San Francisco, CA 94080, USA.
  • Gilbert PB; US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.
  • McElrath MJ; US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.
  • Tomaras GD; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Corey L; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Sci Transl Med ; 11(510)2019 09 18.
Article en En | MEDLINE | ID: mdl-31534016
ABSTRACT
One of the most successful HIV vaccines to date, the RV144 vaccine tested in Thailand, demonstrated correlates of protection including cross-clade V1V2 immunoglobulin G (IgG) breadth, Env-specific CD4+ T cell polyfunctionality, and antibody-dependent cellular cytotoxicity (ADCC) in vaccinees with low IgA binding. The HIV Vaccine Trials Network (HVTN) 097 trial evaluated this vaccine regimen in South Africa, where clade C HIV-1 predominates. We compared cellular and humoral responses at peak and durability immunogenicity time points in HVTN 097 and RV144 vaccinee samples, and evaluated vaccine-matched and cross-clade immune responses. At peak immunogenicity, HVTN 097 vaccinees exhibited significantly higher cellular and humoral immune responses than RV144 vaccinees. CD4+ T cell responses were more frequent in HVTN 097 irrespective of age and sex, and CD4+ T cell Env-specific functionality scores were higher in HVTN 097. Env-specific CD40L+ CD4+ T cells were more common in HVTN 097, with individuals having this pattern of expression demonstrating higher median antibody responses to HIV-1 Env. IgG and IgG3 binding antibody rates and response magnitude to gp120 vaccine- and V1V2 vaccine-matched antigens were higher or comparable in HVTN 097 than in RV144 ADCC, and ADCP functional antibody responses were elicited in HVTN 097. Env-specific IgG and CD4+ Env responses declined significantly over time in both trials. Overall, cross-clade immune responses associated with protection were better than expected in South Africa, suggesting wider applicability of this regimen.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Vacunas contra el SIDA Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male País/Región como asunto: Africa / Asia Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Sudáfrica

Texto completo: 1 Colección: 01-internacional Asunto principal: Vacunas contra el SIDA Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male País/Región como asunto: Africa / Asia Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Sudáfrica