Study Reveals Impact of Third Vaccine Dose in New Zealand
Research shows strong immune response after third Pfizer-BioNTech vaccine dose.
― 6 min read
Table of Contents
- The Arrival of Omicron
- Vaccination Efforts
- Study on Immune Responses
- Study Details
- Ethical Approval
- Demographic Information
- Lab Testing
- Participant Follow-Up
- Findings on Antibody Levels
- Response Across Ethnic Groups
- Impact of Body Mass Index
- Diabetes and Vaccine Response
- Testing Neutralizing Antibodies
- Visual Representation of Findings
- Age as a Factor
- Conclusion
- Original Source
In early 2020, a new virus known as SARS-CoV-2 began to spread worldwide after first being identified in Wuhan, China. This virus causes the disease COVID-19. To combat the spread, New Zealand enforced strict public health rules starting in March 2020. These measures were effective in keeping the virus from spreading widely in the community before vaccines became available in early 2021. As a result, COVID-19 infections were rare in New Zealand, creating a chance to study vaccine responses in a population that had not been widely exposed to the virus.
The Arrival of Omicron
In January 2022, New Zealand saw the arrival of the Omicron variant, a highly contagious strain of the virus. Before that, the country had recorded very few cases, with infections being less than 0.3% of the population. Although the Delta variant had caused some outbreaks in Auckland, most people in New Zealand had not been infected with COVID-19. After Omicron arrived, the patterns of illness and death from COVID-19 in New Zealand began to reflect trends seen in other countries. Older age became a significant risk factor for serious illness and death, and certain ethnic groups, particularly Māori and Pacific peoples, faced higher risks of mortality.
Vaccination Efforts
New Zealand began its national vaccination program in February 2021, rolling out vaccines based on eligibility. By July 2021, most New Zealanders were eligible for vaccination. The Pfizer-BioNTech vaccine was the main one used, making up nearly all doses given. By late 2021, the government recommended a third vaccine dose, initially suggesting it be given six months after the first two doses. However, due to rising cases in early 2022, this interval was shortened to three months.
Despite a strong start to Vaccinations, uptake for the third dose was lower than for the initial two doses, with about 73.2% of adults receiving it.
Study on Immune Responses
This article presents findings from a study called Ka Mātau, Ka Ora, which examines immune responses after vaccinations with the Pfizer-BioNTech vaccine in New Zealand. The participants included those at higher risk for severe COVID-19, such as older adults and people with various health conditions. Previous findings indicated that, after two doses, many people did not show strong immune responses against the Omicron variant.
The current study focused on how Antibody Levels changed after two doses and how a third dose influenced those levels. The participants’ responses were looked at in relation to age, ethnicity, and health conditions.
Study Details
A total of 298 adult participants were involved in this ongoing study, which began in June 2021. The group included those with a higher risk of severe COVID-19, including Māori and Pacific peoples. Participants received two primary doses and a third dose of the Pfizer-BioNTech vaccine between June 2021 and April 2022. Blood samples were collected at set intervals to measure immune responses after vaccination.
Ethical Approval
The New Zealand Health and Disability Ethics Committee approved the study, allowing the research team to gather and analyze data as planned.
Demographic Information
The key demographic factors examined in the study were age, gender, ethnicity, body mass index (BMI), and existing health conditions, including Diabetes. Participants self-reported their ethnic backgrounds, adhering to New Zealand’s guidelines. The study population was diverse, with Māori and Pacific peoples making up a significant portion, and included a range of ages and health statuses.
Lab Testing
Blood samples were tested for specific antibodies related to SARS-CoV-2. Different tests assessed whether participants had been previously infected and how well their immune systems responded to the vaccine. Antibody levels were measured before and after the third vaccine dose, and different tests were used to gauge the strength of the immune response.
Participant Follow-Up
Of the initial participants screened, 298 were enrolled in the study. There were some losses to follow-up, but most participants were tested multiple times for their immune responses. The average time from enrollment to blood sample collection for the third dose was about 238 days.
Findings on Antibody Levels
The study revealed significant changes in antibody levels after the vaccinations. After two vaccine doses, antibody levels were high, but they dropped significantly after six months. However, after receiving the third dose, participants' antibody levels increased dramatically, nearly doubling, indicating a strong immune response to the vaccine.
For different age groups, older participants showed the most considerable improvement after the third dose, suggesting the vaccine effectively boosted immunity in those at higher risk.
Response Across Ethnic Groups
The study also looked at how different ethnic groups responded to the vaccine. Both Māori and Pacific peoples showed strong increases in antibody levels after the third dose. However, there were no significant differences in antibody levels between different ethnicities after receiving the booster shot.
Impact of Body Mass Index
Participants' BMI did not appear to greatly affect the outcome of antibody levels after the second or third vaccine doses. Everyone, regardless of BMI, saw significant increases in antibody levels after the third dose.
Diabetes and Vaccine Response
Interestingly, diabetic participants initially had lower antibody levels compared to non-diabetics after two doses. However, after the third dose, this gap disappeared, and both groups showed significant increases in antibody levels. This finding highlights the importance of a third dose for individuals with diabetes.
Testing Neutralizing Antibodies
The study evaluated how well participants' immune systems could neutralize the virus. Following the second dose, participants had decreased ability to neutralize the virus over time. Most notably, few participants showed the ability to neutralize the Omicron variant after two doses. However, after the third dose, most participants had a strong response against Omicron, reflecting the vaccine's effectiveness.
Visual Representation of Findings
Researchers created maps to visualize the effectiveness of different vaccines in neutralizing various COVID-19 variants. After the third dose, participants showed improved responses to several variants, indicating better protection against the virus.
Age as a Factor
Younger age groups showed stronger responses to the Omicron variant compared to older groups after three doses. This highlights the need for continued monitoring of how different age groups respond to vaccines.
Conclusion
This study emphasizes the strong immune response generated by a third dose of the Pfizer-BioNTech vaccine in New Zealand's largely infection-naïve population. The findings suggest that all demographic groups benefit significantly from the booster shot. Additionally, the results indicate that older adults and those with diabetes also benefit from the additional dose, helping to bolster their immunity against COVID-19.
As the study continues, it will further explore how hybrid immunity develops in response to the virus as more variants emerge. This research is vital for future vaccination strategies and public health policies.
Title: Robust immunogenicity of a third BNT162b2 vaccination against SARS-CoV-2 Omicron variant in a naive New Zealand cohort
Abstract: The ability of a third dose of the Pfizer-BioNTech BNT162b2 SARS-CoV-2 vaccine to stimulate immune responses against subvariants, including Omicron BA.1, has not been assessed in New Zealand populations. Unlike many overseas populations, New Zealanders were largely infection naive at the time they were boosted. This adult cohort of 298 participants, oversampled for at-risk populations, was composed of 29% M[a]ori and 28% Pacific peoples, with 40% of the population aged 55+. A significant proportion of the cohort was obese and presented with at least one comorbidity. Sera were collected 28 days and 6 months post second vaccination and 28 days post third vaccination. SARS-CoV-2 anti-S IgG titres and neutralising capacity using surrogate viral neutralisation assays against variants of concern, including Omicron BA.1, were investigated. The incidence of SARS-CoV-2 infection, within our cohort, prior to third vaccination was very low (
Authors: Brittany Lavender, C. Hooker, C. Frampton, M. Williams, S. Carson, A. Paterson, R. McGregor, N. J. Moreland, K. Gell, F. H. Priddy, K. Wiig, G. Le Gros, J. E. Ussher, M. Brewerton
Last Update: 2023-03-31 00:00:00
Language: English
Source URL: https://www.medrxiv.org/content/10.1101/2023.03.30.23287981
Source PDF: https://www.medrxiv.org/content/10.1101/2023.03.30.23287981.full.pdf
Licence: https://creativecommons.org/licenses/by/4.0/
Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.
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