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Booster Vaccination Against SARS-CoV-2 Induces Potent Immune Responses in People With Human Immunodeficiency Virus.


ABSTRACT:

Background

People with human immunodeficiency virus (HIV) on antiretroviral therapy (ART) with good CD4 T-cell counts make effective immune responses following vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There are few data on longer term responses and the impact of a booster dose.

Methods

Adults with HIV were enrolled into a single arm open label study. Two doses of ChAdOx1 nCoV-19 were followed 12 months later by a third heterologous vaccine dose. Participants had undetectable viraemia on ART and CD4 counts >350 cells/µL. Immune responses to the ancestral strain and variants of concern were measured by anti-spike immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA), MesoScale Discovery (MSD) anti-spike platform, ACE-2 inhibition, activation induced marker (AIM) assay, and T-cell proliferation.

Findings

In total, 54 participants received 2 doses of ChAdOx1 nCoV-19. 43 received a third dose (42 with BNT162b2; 1 with mRNA-1273) 1 year after the first dose. After the third dose, total anti-SARS-CoV-2 spike IgG titers (MSD), ACE-2 inhibition, and IgG ELISA results were significantly higher compared to Day 182 titers (P < .0001 for all 3). SARS-CoV-2 specific CD4+ T-cell responses measured by AIM against SARS-CoV-2 S1 and S2 peptide pools were significantly increased after a third vaccine compared to 6 months after a first dose, with significant increases in proliferative CD4+ and CD8+ T-cell responses to SARS-CoV-2 S1 and S2 after boosting. Responses to Alpha, Beta, Gamma, and Delta variants were boosted, although to a lesser extent for Omicron.

Conclusions

In PWH receiving a third vaccine dose, there were significant increases in B- and T-cell immunity, including to known variants of concern (VOCs).

SUBMITTER: Fidler S 

PROVIDER: S-EPMC9619587 | biostudies-literature | 2023 Jan

REPOSITORIES: biostudies-literature

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Booster Vaccination Against SARS-CoV-2 Induces Potent Immune Responses in People With Human Immunodeficiency Virus.

Fidler Sarah S   Fox Julie J   Tipoe Timothy T   Longet Stephanie S   Tipton Tom T   Abeywickrema Movin M   Adele Sandra S   Alagaratnam Jasmini J   Ali Mohammad M   Aley Parvinder K PK   Aslam Suhail S   Balasubramanian Anbhu A   Bara Anna A   Bawa Tanveer T   Brown Anthony A   Brown Helen H   Cappuccini Federica F   Davies Sophie S   Fowler Jamie J   Godfrey Leila L   Goodman Anna L AL   Hilario Kathrine K   Hackstein Carl-Philipp CP   Mathew Moncy M   Mujadidi Yama F YF   Packham Alice A   Petersen Claire C   Plested Emma E   Pollock Katrina M KM   Ramasamy Maheshi N MN   Robinson Hannah H   Robinson Nicola N   Rongkard Patpong P   Sanders Helen H   Serafimova Teona T   Spence Niamh N   Waters Anele A   Woods Danielle D   Zacharopoulou Panagiota P   Barnes Eleanor E   Dunachie Susanna S   Goulder Philip P   Klenerman Paul P   Winston Alan A   Hill Adrian V S AVS   Gilbert Sarah C SC   Carroll Miles M   Pollard Andrew J AJ   Lambe Teresa T   Ogbe Ane A   Frater John J  

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 20230101 2


<h4>Background</h4>People with human immunodeficiency virus (HIV) on antiretroviral therapy (ART) with good CD4 T-cell counts make effective immune responses following vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There are few data on longer term responses and the impact of a booster dose.<h4>Methods</h4>Adults with HIV were enrolled into a single arm open label study. Two doses of ChAdOx1 nCoV-19 were followed 12 months later by a third heterologous vaccine  ...[more]

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