BNT162b2 mRNA Vaccine-Induced Immune Response in Oral Fluids and Serum

被引:2
作者
Seneviratne, Chaminda Jayampath [1 ,2 ,7 ]
Balan, Preethi [1 ,2 ]
de Alwis, Ruklanthi [3 ,4 ]
Udawatte, Nadeeka S. [1 ]
Herath, Thanuja [1 ,2 ]
Toh, Justin Z. N. [3 ,4 ]
Tin, Goh Bee [1 ]
Ooi, Eng Eong [3 ,4 ]
Hong, Jenny Low Guek [3 ,4 ,5 ]
Ying, Jean Sim Xiang [5 ,6 ]
机构
[1] Natl Dent Res Inst Singapore, Natl Dent Ctr Singapore, Singapore Oral Microbi Initiat, Singapore, Singapore
[2] Duke NUS Med Sch, Oral Hlth ACP, Singapore, Singapore
[3] Duke NUS Med Sch, Program Emerging Infect Dis, Singapore, Singapore
[4] SingHealth Duke NUS Acad Med Ctr, Viral Res & Expt Med Ctr, Singapore, Singapore
[5] Singapore Gen Hosp, Dept Infect Dis, Singapore, Singapore
[6] Singapore Gen Hosp, Dept Infect Prevent & Epidemiol, Singapore, Singapore
[7] Natl Dent Res Inst Singapore NDRIS, Natl Dent Ctr Singapore, Singapore Oral Microbi Inititat SOMI, SingHealth Duke NUS, Singapore, Singapore
关键词
Key COVID-19 vaccines; Gingival crevicular fluid; Saliva; Immunity; GINGIVAL CREVICULAR FLUID; SALIVA; ANTIBODIES; TESTS;
D O I
10.1016/j.identj.2022.09.005
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: The COVID-19 vaccine is currently being administered worldwide to address the ongoing pandemic. Although these vaccines have proven effective in preventing severe disease, the level of immunity required to prevent respiratory mucosal infection remains less well understood. Therefore, it is desirable to develop a noninvasive screening strategy such as oral fluid to monitor secreted antibodies longitudinally as potential surrogates of mucosal immunity. Methods: We evaluated the anti-spike protein antibodies in gingival crevicular fluid (GCF) and saliva and compared them to immune responses in the blood of 50 healthy health care workers following 2 doses of intramuscular Pfizer/BioNTech-BNT162b2 vaccine. Results: The antibodies to SARS-CoV-2 spike and subdomain proteins (RBD, S1, S2, and NTD) were significantly higher in serum than oral fluids but showed a greater detection rate and higher median titres in GCF than saliva. For all tested SARS-CoV-2 antigens, IgG in GCF (as opposed to saliva) showed a more significant and stronger correlation with IgG in serum. Serum-neutralising antibodies (Nab) titres also displayed a significant and stronger correlation with anti-spike protein and their subdomains in GCF than saliva. Interestingly, the time post -second dose of vaccine and sex had a similar influence on IgG in serum and GCF. However, interferon (IFN)-g-producing T-cell responses showed no association with SARS-Cov-2 IgG anti-bodies in serum, GCF, or saliva and neutralisation antibodies in serum. The correlation matrix of all measured parameters grouped serum and GCF IgG parameters separately from salivary IgG parameters indicating that GCF better represents the humoural response in serum than saliva. Conclusions: Within limitations, we propose that GCF could be a less invasive alternative to serum and more appropriate than saliva to detect antibody responses by current COVID-19 vaccines if the GCF collection procedure could be standardised. Further research is needed to investigate the suitability of GCF for community immune surveillance for vaccines. (c) 2022 Published by Elsevier Inc. on behalf of FDI World Dental Federation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:435 / 442
页数:8
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