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. 2023 Aug 1;19(2):2251850.
doi: 10.1080/21645515.2023.2251850.

The immunogenicity of the ChAdOx1 nCoV-19 vaccination in participants with underlying comorbidity diseases: A prospective cohort study

Affiliations

The immunogenicity of the ChAdOx1 nCoV-19 vaccination in participants with underlying comorbidity diseases: A prospective cohort study

Thachanun Porntharukchareon et al. Hum Vaccin Immunother. .

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) increases mortality rates in older adults and those with comorbidities. Individuals with certain comorbidities may have a poor immune response and require early booster vaccines. We aimed to assess the immune response after two doses of ChAdOx1 nCoV-19 vaccine, at 84-day intervals, in participants with the following comorbidities; diabetes mellitus; obesity; cardiovascular disease; chronic kidney disease; rheumatological disease; cirrhosis; hematological disease; hematological malignancy; or solid malignancy. The study was conducted at Chulabhorn Hospital in Thailand, with healthy healthcare workers serving as the control group. Of the 769 participants, 352 were in the healthy cohort and 417 were in the comorbidity cohort, all received at least one dose of vaccine. Anti-RBD total antibody levels were evaluated on Day 0, Day 84, and Day 112. The results at Day 112 (4 weeks after the second dose) showed that individuals with comorbidities had a poor immune response compared to healthy individuals, especially those with hematological malignancy and solid malignancy. The geometric mean concentration (GMC) of anti-RBD antibody in the comorbidity cohort was significantly lower than that in the healthy cohort: 433.66 BAU/ml (95% CI 334.62-562.01) versus 1096.14 BAU/ml (95% CI 1010.26-1189.33), respectively. The geometric mean ratio (GMR) between the two cohorts was 0.40 (95% CI 0.30-0.52, p < .001). This study concluded that individuals with comorbidities, particularly hematological and solid malignancies, had poor immune responses and may require an early booster vaccine to prevent infection and death.

Keywords: COVID-19; ChAdOx1 nCoV-19; comorbidity; immunogenicity; vaccine.

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Conflict of interest statement

No potential conflict of interest was reported by the author(s).

Figures

Figure 1.
Figure 1.
Participants’ flow. DM: diabetes mellitus. n: number of participants.
Figure 2.
Figure 2.
The geometric mean concentration of anti-RBD antibodies in the comorbidity cohort and healthy cohort at 3 months after 1st vaccination and 1 month after 2nd vaccination (4 months).
Figure 3.
Figure 3.
Subgroup analysis of anti-RBD antibody level at 3 months after 1st dose of ChAdOx1 nCoV-19 vaccine and 1 month after 2nd dose of ChAdOx1 nCoV-19 vaccine. Figure 3a demonstrates anti-SARS-CoV2 IgG Ab level at 3 months after 1st dose of the ChAdOx1 nCoV-19 vaccine. Figure 3b demonstrates anti-SARS-CoV2 IgG Ab level at 1 month after 2nd dose of the ChAdOx1 nCoV-19 vaccine. BAU: binding antibody unit. Hemato: hematological disease (benign). Hemato onco (hematological malignancy). Onco malignancy: solid cancer. CKD: chronic kidney disease. Rheumato: rheumatological disease. Cardio: cardiovascular disease. DM: diabetes mellitus.
Figure 4.
Figure 4.
Geometric mean and standard deviation of anti-RBD spike protein of SARS-CoV-2 level (Bau/ml) after vaccination (months). RBD: receptor binding domain. BAU: binding antibody unit. SARS-CoV-2: severe acute respiratory syndrome coronavirus 2.

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