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Viral vector delivered immunogen focuses HIV-1 antibody specificity and increases durability of the circulating antibody recall response.
Williams, LaTonya D; Shen, Xiaoying; Sawant, Sheetal S; Akapirat, Siriwat; Dahora, Lindsay C; Tay, Matthew Zirui; Stanfield-Oakley, Sherry; Wills, Saintedym; Goodman, Derrick; Tenney, DeAnna; Spreng, Rachel L; Zhang, Lu; Yates, Nicole L; Montefiori, David C; Eller, Michael A; Easterhoff, David; Hope, Thomas J; Rerks-Ngarm, Supachai; Pittisuttithum, Punnee; Nitayaphan, Sorachai; Excler, Jean-Louis; Kim, Jerome H; Michael, Nelson L; Robb, Merlin L; O'Connell, Robert J; Karasavvas, Nicos; Vasan, Sandhya; Ferrari, Guido; Tomaras, Georgia D.
Afiliação
  • Williams LD; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Shen X; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Sawant SS; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Akapirat S; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Dahora LC; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Tay MZ; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Stanfield-Oakley S; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Wills S; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Goodman D; Department of Retrovirology, US Army Medical Directorate, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
  • Tenney D; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Spreng RL; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Zhang L; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Yates NL; Department of Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Montefiori DC; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Eller MA; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Easterhoff D; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Hope TJ; Department of Molecular Genetics Microbiology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Rerks-Ngarm S; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Pittisuttithum P; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Nitayaphan S; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Excler JL; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Kim JH; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Michael NL; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Robb ML; Department of Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • O'Connell RJ; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Karasavvas N; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Vasan S; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Ferrari G; Center for Human Systems Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Tomaras GD; Department of Surgery, Duke University School of Medicine, Durham, North Carolina, United States of America.
PLoS Pathog ; 19(5): e1011359, 2023 05.
Article em En | MEDLINE | ID: mdl-37256916
The modestly efficacious HIV-1 vaccine regimen (RV144) conferred 31% vaccine efficacy at 3 years following the four-shot immunization series, coupled with rapid waning of putative immune correlates of decreased infection risk. New strategies to increase magnitude and durability of protective immunity are critically needed. The RV305 HIV-1 clinical trial evaluated the immunological impact of a follow-up boost of HIV-1-uninfected RV144 recipients after 6-8 years with RV144 immunogens (ALVAC-HIV alone, AIDSVAX B/E gp120 alone, or ALVAC-HIV + AIDSVAX B/E gp120). Previous reports demonstrated that this regimen elicited higher binding, antibody Fc function, and cellular responses than the primary RV144 regimen. However, the impact of the canarypox viral vector in driving antibody specificity, breadth, durability and function is unknown. We performed a follow-up analysis of humoral responses elicited in RV305 to determine the impact of the different booster immunogens on HIV-1 epitope specificity, antibody subclass, isotype, and Fc effector functions. Importantly, we observed that the ALVAC vaccine component directly contributed to improved breadth, function, and durability of vaccine-elicited antibody responses. Extended boosts in RV305 increased circulating antibody concentration and coverage of heterologous HIV-1 strains by V1V2-specific antibodies above estimated protective levels observed in RV144. Antibody Fc effector functions, specifically antibody-dependent cellular cytotoxicity and phagocytosis, were boosted to higher levels than was achieved in RV144. V1V2 Env IgG3, a correlate of lower HIV-1 risk, was not increased; plasma Env IgA (specifically IgA1), a correlate of increased HIV-1 risk, was elevated. The quality of the circulating polyclonal antibody response changed with each booster immunization. Remarkably, the ALVAC-HIV booster immunogen induced antibody responses post-second boost, indicating that the viral vector immunogen can be utilized to selectively enhance immune correlates of decreased HIV-1 risk. These results reveal a complex dynamic of HIV-1 immunity post-vaccination that may require careful balancing to achieve protective immunity in the vaccinated population. Trial registration: RV305 clinical trial (ClinicalTrials.gov number, NCT01435135). ClinicalTrials.gov Identifier: NCT00223080.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Problema de saúde: 1_doencas_nao_transmissiveis / 2_enfermedades_transmissibles Assunto principal: Infecções por HIV / HIV-1 / Soropositividade para HIV / Vacinas contra a AIDS Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: PLoS Pathog Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Problema de saúde: 1_doencas_nao_transmissiveis / 2_enfermedades_transmissibles Assunto principal: Infecções por HIV / HIV-1 / Soropositividade para HIV / Vacinas contra a AIDS Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: PLoS Pathog Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
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