Back

Titers and capacity of neutralizing antibodies against SARS-CoV-2 variants after heterologous booster vaccination in health care workers primed with two doses of ChAdOx1 nCov-19: a single-blinded, randomized clinical trial

Chuang, C.-H.; Huang, C.-G.; Huang, C.-T.; Chen, Y.-C.; Kung, Y.-A.; Chen, C.-J.; Chuang, T.-C.; Liu, C.-C.; Huang, P.-W.; Yang, S.-L.; Gu, P.-W.; Shih, S.-R.; Chiu, C.-H.

2022-06-16 infectious diseases
10.1101/2022.06.14.22276236 medRxiv
Show abstract

BackgroundBooster vaccination is important because of waning immunity and variant immune evasion. We conducted a single-blinded, randomized trial to evaluate the safety, reactogenicity, and immunogenicity of heterologous booster vaccination in health care workers (HCW) who had received two doses of ChAdOx1 nCov-19. Methods and findingsHCW at least 90 days after the second dose were enrolled to receive one of the four vaccines: BNT162b2, half-dose mRNA-1273, mRNA-1273, and MVC-COV1901. The primary outcomes were humoral and cellular immunogenicity and the secondary outcomes safety and reactogenicity 28 days post-booster. 340 HCW were enrolled: 83 received BNT162b2 (2 excluded), 85 half-dose mRNA-1273, 85 mRNA-1273, and 85 MVC-COV1901. mRNA vaccines had more reactogenicity than protein vaccine. Anti-spike IgG increased by a fold of 8.4 for MCV-COV1901, 32.2 for BNT162b2, 47.6 for half-dose mRNA-1273 and 63.2 for mRNA1273. The live virus microneutralization assay (LVMNA) against the wild type, alpha and delta variants were consistent with anti-spike IgG for all booster vaccines. The LVMNA in the four groups against omicron variant were 6.4 to 13.5 times lower than those against the wild type. Serum neutralizing antibody against omicron variant was undetectable in 60% of the participants who received MCV-COV1901 as a booster by LVMNA. By using pseudovirus neutralizing assay, we found that neutralization activity in the four groups against omicron variant were 4.6 to 5.2 times lower than that against the D614G. All booster vaccines induced comparable T cell response. ConclusionsThird dose booster not only increases neutralizing antibody titer but also enhances antibody capacity against SARS-CoV-2 variants. mRNA vaccines are preferred booster vaccines for those after primary series of ChAdOx1 nCov-19. Trial registrationClinicalTrials.gov NCT05132855

Matching journals

The top 3 journals account for 50% of the predicted probability mass.

1
New England Journal of Medicine
50 papers in training set
Top 0.1%
32.3%
2
Clinical Infectious Diseases
231 papers in training set
Top 0.2%
14.0%
3
The Lancet Infectious Diseases
71 papers in training set
Top 0.1%
14.0%
50% of probability mass above
4
Vaccine
189 papers in training set
Top 0.5%
6.7%
5
JAMA Network Open
127 papers in training set
Top 1%
3.5%
6
PLOS Medicine
98 papers in training set
Top 2%
2.7%
7
Open Forum Infectious Diseases
134 papers in training set
Top 0.7%
2.7%
8
The Journal of Infectious Diseases
182 papers in training set
Top 3%
1.7%
9
Nature Communications
4913 papers in training set
Top 52%
1.7%
10
Journal of Infection
71 papers in training set
Top 2%
1.5%
11
The Lancet Respiratory Medicine
17 papers in training set
Top 0.1%
1.5%
12
eClinicalMedicine
55 papers in training set
Top 1%
1.1%
13
Annals of Internal Medicine
27 papers in training set
Top 0.8%
0.9%
14
BMC Medicine
163 papers in training set
Top 6%
0.9%
15
Emerging Infectious Diseases
103 papers in training set
Top 3%
0.8%
16
Nature Medicine
117 papers in training set
Top 5%
0.7%
17
Human Vaccines & Immunotherapeutics
25 papers in training set
Top 0.8%
0.7%
18
BMJ
49 papers in training set
Top 1%
0.7%
19
The Lancet
16 papers in training set
Top 0.8%
0.7%
20
JAMA
17 papers in training set
Top 0.4%
0.7%
21
PLOS ONE
4510 papers in training set
Top 70%
0.7%
22
Clinical Microbiology and Infection
60 papers in training set
Top 2%
0.6%