JCI Insight (Apr 2022)

Durability of ChAdOx1 nCoV-19 vaccination in people living with HIV

  • Ane Ogbe,
  • Matthew Pace,
  • Mustapha Bittaye,
  • Timothy Tipoe,
  • Sandra Adele,
  • Jasmini Alagaratnam,
  • Parvinder K. Aley,
  • M. Azim Ansari,
  • Anna Bara,
  • Samantha Broadhead,
  • Anthony Brown,
  • Helen Brown,
  • Federica Cappuccini,
  • Paola Cinardo,
  • Wanwisa Dejnirattisai,
  • Katie J. Ewer,
  • Henry Fok,
  • Pedro M. Folegatti,
  • Jamie Fowler,
  • Leila Godfrey,
  • Anna L. Goodman,
  • Bethany Jackson,
  • Daniel Jenkin,
  • Mathew Jones,
  • Stephanie Longet,
  • Rebecca A. Makinson,
  • Natalie G. Marchevsky,
  • Moncy Mathew,
  • Andrea Mazzella,
  • Yama F. Mujadidi,
  • Lucia Parolini,
  • Claire Petersen,
  • Emma Plested,
  • Katrina M. Pollock,
  • Thurkka Rajeswaran,
  • Maheshi N. Ramasamy,
  • Sarah Rhead,
  • Hannah Robinson,
  • Nicola Robinson,
  • Helen Sanders,
  • Sonia Serrano,
  • Tom Tipton,
  • Anele Waters,
  • Panagiota Zacharopoulou,
  • Eleanor Barnes,
  • Susanna Dunachie,
  • Philip Goulder,
  • Paul Klenerman,
  • Gavin R. Screaton,
  • Alan Winston,
  • Adrian V.S. Hill,
  • Sarah C. Gilbert,
  • Miles Carroll,
  • Andrew J. Pollard,
  • Sarah Fidler,
  • Julie Fox,
  • Teresa Lambe,
  • John Frater

Journal volume & issue
Vol. 7, no. 7

Abstract

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Duration of protection from SARS-CoV-2 infection in people living with HIV (PWH) following vaccination is unclear. In a substudy of the phase II/III the COV002 trial (NCT04400838), 54 HIV+ male participants on antiretroviral therapy (undetectable viral loads, CD4+ T cells > 350 cells/μL) received 2 doses of ChAdOx1 nCoV-19 (AZD1222) 4–6 weeks apart and were followed for 6 months. Responses to vaccination were determined by serology (IgG ELISA and Meso Scale Discovery [MSD]), neutralization, ACE-2 inhibition, IFN-γ ELISpot, activation-induced marker (AIM) assay and T cell proliferation. We show that, 6 months after vaccination, the majority of measurable immune responses were greater than prevaccination baseline but with evidence of a decline in both humoral and cell-mediated immunity. There was, however, no significant difference compared with a cohort of HIV-uninfected individuals vaccinated with the same regimen. Responses to the variants of concern were detectable, although they were lower than WT. Preexisting cross-reactive T cell responses to SARS-CoV-2 spike were associated with greater postvaccine immunity and correlated with prior exposure to beta coronaviruses. These data support the ongoing policy to vaccinate PWH against SARS-CoV-2, and they underpin the need for long-term monitoring of responses after vaccination.

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