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Strong Neutralizing Antibody Responses to SARS-CoV-2 Variants Following a Single Vaccine Dose in Subjects With Previous SARS-CoV-2 Infection

Ekström Nina; Haveri Anu; Solastie Anna; Virta; Camilla; Österlund Pamela; Nohynek Hanna; Nieminen Tuomo; Ivaska Lauri; Tähtinen Paula A.; Lempainen Johanna; Jalkanen Pinja; Julkunen Ilkka; Palmu Arto A.; Melin Merit

Strong Neutralizing Antibody Responses to SARS-CoV-2 Variants Following a Single Vaccine Dose in Subjects With Previous SARS-CoV-2 Infection

Ekström Nina
Haveri Anu
Solastie Anna
Virta
Camilla
Österlund Pamela
Nohynek Hanna
Nieminen Tuomo
Ivaska Lauri
Tähtinen Paula A.
Lempainen Johanna
Jalkanen Pinja
Julkunen Ilkka
Palmu Arto A.
Melin Merit
Katso/Avaa
ofac625.pdf (811.8Kb)
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OXFORD UNIV PRESS INC
doi:10.1093/ofid/ofac625
URI
https://www.doi.org/10.1093/ofid/ofac625
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe202301286329
Tiivistelmä

Background: Previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection primes the immune system; thus individuals who have recovered from infection have enhanced immune responses to subsequent vaccination (hybrid immunity). However, it remains unclear how well hybrid immunity induced by severe or mild infection can cross-neutralize emerging variants. We aimed to compare the strength and breadth of antibody responses in vaccinated recovered and uninfected subjects.

Methods: We measured spike-specific immunoglobulin (Ig)G and neutralizing antibodies (NAbs) from vaccinated subjects including 320 with hybrid immunity and 20 without previous infection. From 29 subjects with a previous severe or mild infection, we also measured NAb responses against Alpha (B.1.1.7), Beta (B.1.351), Delta (B.1.617.2), and Omicron (B.1.1.529/BA.1) variants following vaccination.

Results: A single vaccine dose induced 2-fold higher anti-spike IgG concentrations and up to 4-fold higher neutralizing potency of antibodies in subjects with a previous infection compared with vaccinated subjects without a previous infection. Hybrid immunity was more enhanced after a severe than a mild infection, with sequentially decreasing NAb titers against Alpha, Beta, Delta, and Omicron variants. We found similar IgG concentrations in subjects with a previous infection after 1 or 2 vaccine doses.

Conclusions: Hybrid immunity induced strong IgG responses, particularly after severe infection. However, the NAb titers were low against heterologous variants, especially against Omicron.

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