Establishment of Reference Reagents for Single-Radial-Immunodiffusion Assay on the 2022/23 Seasonal Influenza Vaccine in Japan and Their Quality Validation

• Published in: Japanese Journal of Infectious Diseases Vol. 77; no. 2; pp. 105 - 111
• Main Authors: Shimasaki, Noriko, Kuwahara, Tomoko, Nishijima, Haruna, Nakamura, Kazuya, Sato, Kayoko, Murano, Keiko, Itamura, Shigeyuki, Akahori, Yukiko, Takashita, Emi, Kishida, Noriko, Arita, Tomoko, Nakauchi, Mina, Takeda, Makoto, Hasegawa, Hideki, Ryo, Akihide, Harada, Yuichi
• Format: Journal Article
• Language: English
• Published: Japan National Institute of Infectious Diseases 29.03.2024; Japan Science and Technology Agency
• Subjects: Antigens; Antisera; Assaying; Cross-reactivity; HA protein; Hemagglutinins; Immunodiffusion; Influenza; Influenza B; influenza B virus component; Quality control; quality validation; Reagents; reference reagent; seasonal influenza vaccine; single-radial-immunodiffusion assay; Vaccines; Japan; reference reagent; influenza B virus component; quality validation; seasonal influenza vaccine; single-radial-immunodiffusion assay
• ISSN: 1344-6304; 1884-2836; 1884-2836
• DOI: 10.7883/yoken.JJID.2023.218

Potency tests for influenza vaccines are currently performed using a single-radial immunodiffusion (SRID) assay, which requires a reference antigen and anti-hemagglutinin (HA) serum as reference reagents. Reagents must be newly prepared each time a strain used for vaccine production is modified. Therefore, establishing reference reagents of consistent quality is crucial for conducting vaccine potency tests accurately and precisely. Here, we established reference reagents for the SRID assay to conduct lot release tests of quadrivalent influenza vaccines in Japan during the 2022/23 influenza season. The potency of reference antigens during storage was confirmed. Furthermore, we evaluated the cross-reactivity of each antiserum raised against the HA protein of the 2 lineages of influenza B virus toward different lineages of influenza B virus antigens to select a suitable procedure for the SRID assay for accurate measurement. Finally, the intralaboratory reproducibility of the SRID assay using the established reference reagents was validated, and the SRID reagents had sufficient consistent quality, comparable to that of the reagents used for testing vaccines during previous influenza seasons. Our study contributes to the quality control of influenza vaccines.