Varying Cellular Immune Response against SARS-CoV-2 after the Booster Vaccination: A Cohort Study from Fukushima Vaccination Community Survey, Japan

Author:

Tani Yuta1,Takita Morihito12ORCID,Kobashi Yurie23,Wakui Masatoshi4,Zhao Tianchen2,Yamamoto Chika2,Saito Hiroaki25ORCID,Kawashima Moe2,Sugiura Sota1,Nishikawa Yoshitaka3,Omata Fumiya3,Shimazu Yuzo3ORCID,Kawamura Takeshi67,Sugiyama Akira6,Nakayama Aya6,Kaneko Yudai78,Kodama Tetsuhiko7,Kami Masahiro1,Tsubokura Masaharu235ORCID

Affiliation:

1. Medical Governance Research Institute, Tokyo 108-0074, Japan

2. Department of Radiation Health Management, Fukushima Medical University, Fukushima 960-1295, Japan

3. Department of General Internal Medicine, Hirata Central Hospital, Fukushima 963-8202, Japan

4. Department of Laboratory Medicine, Keio University School of Medicine, Tokyo 160-0016, Japan

5. Department of Internal Medicine, Soma Central Hospital, Fukushima 976-0016, Japan

6. Proteomics Laboratory, Isotope Science Center, The University of Tokyo, Tokyo 113-0032, Japan

7. Laboratory for Systems Biology and Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan

8. Medical and Biological Laboratories Co., Ltd., Tokyo 105-0012, Japan

Abstract

Booster vaccination reduces the incidence of severe cases and mortality related to COVID-19, with cellular immunity playing an important role. However, little is known about the proportion of the population that has achieved cellular immunity after booster vaccination. Thus, we conducted a Fukushima cohort database and assessed humoral and cellular immunity in 2526 residents and healthcare workers in Fukushima Prefecture in Japan through continuous blood collection every 3 months from September 2021. We identified the proportion of people with induced cellular immunity after booster vaccination using the T-SPOT.COVID test, and analyzed their background characteristics. Among 1089 participants, 64.3% (700/1089) had reactive cellular immunity after booster vaccination. Multivariable analysis revealed the following independent predictors of reactive cellular immunity: age < 40 years (adjusted odds ratio: 1.81; 95% confidence interval: 1.19–2.75; p-value: 0.005) and adverse reactions after vaccination (1.92, 1.19–3.09, 0.007). Notably, despite IgG(S) and neutralizing antibody titers of ≥500 AU/mL, 33.9% (349/1031) and 33.5% (341/1017) of participants, respectively, did not have reactive cellular immunity. In summary, this is the first study to evaluate cellular immunity at the population level after booster vaccination using the T-SPOT.COVID test, albeit with several limitations. Future studies will need to evaluate previously infected subjects and their T-cell subsets.

Funder

AMED Development of Vaccines for the Novel Coronavirus Disease

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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