ChAdOx1 nCoV-19 coronavirus vaccine: Long-term safety and immunological responses.

Publication date: Jul 19, 2026

Follow-up of pre-licensure trial participants potentially informs a vaccine’s long-term safety profile. This prospective study enrolled participants from the first clinical trials of ChAdOx1 nCoV-19 vaccine, many of whom subsequently received COVID-19 vaccines in the UK vaccination programme. Serious adverse events (SAEs) and adverse events of special interest (AESIs) were captured. AESI selection was based on Brighton Collaboration definitions. Between September 2021 and April 2022, 4470 participants enrolled (58% female, median age 50 years); 3845/4470 (86. 0%) completed the study. Median follow-up was 11. 77 months; total follow-up was 48,116 person-months. There were 174 SAEs and 71 AESIs (33 events recorded as both) in 195 participants, including 5 deaths. Immunology data were available for a small subset of participants; total IgG against trimeric SARS-CoV-2 spike protein tended to increase during the study. Although no emergent safety signals were detected, continued post-marketing surveillance remains imperative, particularly for neurological disorders. 2021-003382-36.

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Concepts Keywords
Adenoviral vector vaccine
AZD1222
Booster vaccine
Covishield
Pandemic
Vaxzevria

Semantics

Type Source Name
disease MESH neurological disorders
drug DRUGBANK Abacavir
disease MESH David
disease MESH NHS
disease MESH Infection
disease MESH Park
disease MESH Infectious Diseases
drug DRUGBANK Thiamine
drug DRUGBANK Coenzyme M
disease MESH COVID 19 pandemic
disease MESH included
disease MESH Guillain Barre syndrome
disease MESH transverse myelitis
disease MESH capillary leak syndrome
disease MESH thrombosis
disease MESH syndrome
disease MESH death
disease MESH birth defect
disease MESH stroke

Original Article

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