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Oxford University Press - PMC COVID-19 Collection logoLink to Oxford University Press - PMC COVID-19 Collection
. 2021 Apr 27:ciab381. doi: 10.1093/cid/ciab381

Age-dependent immune response to the Biontech/Pfizer BNT162b2 COVID-19 vaccination

Lisa Müller 1,#,, Marcel Andrée 1,#, Wiebke Moskorz 1, Ingo Drexler 1, Lara Walotka 1, Ramona Grothmann 1, Johannes Ptok 1, Jonas Hillebrandt 1,2, Anastasia Ritchie 1, Denise Rabl 1, Philipp Niklas Ostermann 1, Rebekka Robitzsch 1, Sandra Hauka 1, Andreas Walker 1, Christopher Menne 1, Ralf Grutza 1, Jörg Timm 1, Ortwin Adams 1,#, Heiner Schaal 1,#
PMCID: PMC8135422  PMID: 33906236

Abstract

Background

The SARS-CoV-2 pandemic has led to the development of various vaccines. Real-life data on immune responses elicited in the most vulnerable group of vaccinees over 80 years old is still underrepresented despite the prioritization of the elderly in vaccination campaigns.

Methods

We conducted a cohort study with two age groups, young vaccinees below the age of 60 and elderly vaccinees over the age of 80, to compare their antibody responses to the first and second dose of the BNT162b2 COVID-19 vaccination.

Results

While the majority of participants in both groups produced specific IgG antibody titers against SARS-CoV-2 spike protein, titers were significantly lower in elderly participants. Although the increment of antibody levels after the second immunization was higher in elderly participants, the absolute mean titer of this group remained lower than the <60 group. After the second vaccination, 31.3 % of the elderly had no detectable neutralizing antibodies in contrast to the younger group, in which only 2.2% had no detectable neutralizing antibodies.

Conclusion

Our data showed differences between the antibody responses raised after the first and second BNT162b2 vaccination, in particular lower frequencies of neutralizing antibodies in the elderly group. This suggests that this population needs to be closely monitored and may require earlier revaccination or/and an increased vaccine dose to ensure stronger long lasting immunity and protection against infection.


Articles from Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America are provided here courtesy of Oxford University Press

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