Vaccines against SARS-CoV-2 have been pivotal in overcoming the
COVID-19 pandemic yet understanding the subsequent outcomes and immunological effects remain crucial, especially for at-risk groups e.g., people living with human immunodeficiency virus (HIV) (PLWH). In this study we report the longitudinal
IgA and
IgG antibody titers, as well as antibody-mediated
angiotensin converting enzyme 2 (ACE2) binding blockade, against the SARS-CoV-2 spike (S)
proteins after 1 and 2 doses of the
ChAdOx1 nCoV-19 vaccine in a population of Black PLWH. Here, we report that PLWH (N = 103) did not produce an anti-S
IgA response after
infection or vaccination, however, anti-S
IgG was detected in response to vaccination and
infection, with the highest level detected for infected vaccinated participants. The
anti-IgG and ACE2 blockade assays revealed that both vaccination and
infection resulted in
IgG production, however, only vaccination resulted in a moderate increase in ACE2 binding blockade to the ancestral S
protein. Vaccination with a previous
infection results in the greatest anti-S
IgG and ACE2 blockade for the ancestral S
protein. In conclusion, PLWH produce an anti-S
IgG response to the
ChAdOx1 nCoV-19 vaccine and/or
infection, and
ChAdOx1 nCoV-19 vaccination with a previous
infection produced more
neutralizing antibodies than vaccination alone.