tetano
Editor, Senior Moderator
Vaccine
. 2024 Oct 16;42(26):126452.
doi: 10.1016/j.vaccine.2024.126452. Online ahead of print. Cellular and humoral immunity and IgG subclass distribution after omicron XBB.1.5 monovalent vaccination in Japan
Kaori Sano[SUP] 1 [/SUP], Takayuki Kurosawa[SUP] 2 [/SUP], Kazuo Horikawa[SUP] 3 [/SUP], Yayoi Kimura[SUP] 4 [/SUP], Atsushi Goto[SUP] 5 [/SUP], Akihide Ryo[SUP] 6 [/SUP], Hideki Hasegawa[SUP] 7 [/SUP], Hideaki Kato[SUP] 8 [/SUP], Kei Miyakawa[SUP] 9 [/SUP]
Affiliations
Background: Up to seven doses of coronavirus disease 2019 (COVID-19) mRNA vaccines (BNT162b2) were administered to Japanese healthcare workers, until February 2024. The monovalent Omicron XBB.1.5 vaccine (hereafter called XBB.1.5 vaccine) was used for dose 7.
Objective: Although the XBB.1.5 vaccine has been reported to induce a robust increase in neutralizing antibodies against the currently circulating Omicron variant BA.2.86, little is known about its serological effects in Japan, where the BNT162b2 mRNA vaccine is the most frequently administered in the world.
Study design: Twenty-five recipients of the XBB.1.5 vaccine, categorized as seronegative (n = 18) or seropositive (n = 7) based on their recent history of COVID-19, were analyzed. Neutralizing antibody titers against Omicron subvariants, receptor binding domain (RBD) IgG levels, IgG subclass distribution, and T-cell responses were assessed.
Results: We found a significant increase in neutralizing antibody titers against XBB.1.5 and BA.2.86 variants following XBB.1.5 vaccination, particularly in seropositive individuals. No significant change in total RBD IgG levels was observed, indicating efficient induction of antibodies targeting regions outside the RBD by XBB.1.5 vaccination. IgG subclass analysis demonstrated no significant subclass switching after vaccination. T-cell responses against the virus were comparable between seropositive and seronegative groups.
Conclusions: The study suggests that XBB.1.5 vaccination enhances humoral immunity against Omicron variants without significant IgG subclass switching. However, some individuals with low pre-vaccination IgG titers did not exhibit increased antibody levels post-vaccination, raising concerns about potential immune tolerance.
. 2024 Oct 16;42(26):126452.
doi: 10.1016/j.vaccine.2024.126452. Online ahead of print. Cellular and humoral immunity and IgG subclass distribution after omicron XBB.1.5 monovalent vaccination in Japan
Kaori Sano[SUP] 1 [/SUP], Takayuki Kurosawa[SUP] 2 [/SUP], Kazuo Horikawa[SUP] 3 [/SUP], Yayoi Kimura[SUP] 4 [/SUP], Atsushi Goto[SUP] 5 [/SUP], Akihide Ryo[SUP] 6 [/SUP], Hideki Hasegawa[SUP] 7 [/SUP], Hideaki Kato[SUP] 8 [/SUP], Kei Miyakawa[SUP] 9 [/SUP]
Affiliations
- PMID: 39418690
- DOI: 10.1016/j.vaccine.2024.126452
Background: Up to seven doses of coronavirus disease 2019 (COVID-19) mRNA vaccines (BNT162b2) were administered to Japanese healthcare workers, until February 2024. The monovalent Omicron XBB.1.5 vaccine (hereafter called XBB.1.5 vaccine) was used for dose 7.
Objective: Although the XBB.1.5 vaccine has been reported to induce a robust increase in neutralizing antibodies against the currently circulating Omicron variant BA.2.86, little is known about its serological effects in Japan, where the BNT162b2 mRNA vaccine is the most frequently administered in the world.
Study design: Twenty-five recipients of the XBB.1.5 vaccine, categorized as seronegative (n = 18) or seropositive (n = 7) based on their recent history of COVID-19, were analyzed. Neutralizing antibody titers against Omicron subvariants, receptor binding domain (RBD) IgG levels, IgG subclass distribution, and T-cell responses were assessed.
Results: We found a significant increase in neutralizing antibody titers against XBB.1.5 and BA.2.86 variants following XBB.1.5 vaccination, particularly in seropositive individuals. No significant change in total RBD IgG levels was observed, indicating efficient induction of antibodies targeting regions outside the RBD by XBB.1.5 vaccination. IgG subclass analysis demonstrated no significant subclass switching after vaccination. T-cell responses against the virus were comparable between seropositive and seronegative groups.
Conclusions: The study suggests that XBB.1.5 vaccination enhances humoral immunity against Omicron variants without significant IgG subclass switching. However, some individuals with low pre-vaccination IgG titers did not exhibit increased antibody levels post-vaccination, raising concerns about potential immune tolerance.