Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection
Иммунологическая память к SARS-CoV-2 оценивалась в течение до 8 месяцев после инфекции
2021-01-06
SCID: 54.1/peq86mnf
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SARS-CoV-2 immune memorySARS-CoV-2-specific CD4+ T cellsSARS-CoV-2-specific CD8+ T cellsSpike-specific IgGSpike-specific memory B cells
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Abstract (AI)
Variable memory Immune memory against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) helps to determine protection against reinfection, disease risk, and vaccine efficacy. Using 188 human cases across the range of severity of COVID-19, Dan et al. analyzed cross-sectional data describing the dynamics of SARS-CoV-2 memory B cells, CD8 + T cells, and CD4 + T cells for more than 6 months after infection. The authors found a high degree of heterogeneity in the magnitude of adaptive immune responses that persisted into the immune memory phase to the virus. However, immune memory in three immunological compartments remained measurable in greater than 90% of subjects for more than 5 months after infection. Despite the heterogeneity of immune responses, these results show that durable immunity against secondary COVID-19 disease is a possibility for most individuals. Science , this issue p. eabf4063
Key Findings
1
Different components of SARS-CoV-2 immune memory (antibodies, memory B cells, CD4+ T cells, CD8+ T cells) show distinct kinetic profiles when assessed together.
2
IgG antibodies to the SARS-CoV-2 spike protein remained relatively stable for at least 6+ months after infection.
3
SARS-CoV-2-specific CD4+ and CD8+ T cells declined over time with estimated half-lives of approximately 3 to 5 months.
4
Spike-specific memory B cells increased in abundance by 6 months compared to 1 month after symptom onset.
5
The study analyzed multiple immune memory compartments in 254 samples from 188 COVID-19 cases, including 43 samples at ≥6 months post-infection.
Research Object
Circulating immune memory to SARS-CoV-2 in recovered COVID-19 cases
Research Subject
Kinetics and durability of multiple immune-memory compartments (spike-specific IgG, memory B cells, CD4+ T cells, CD8+ T cells) up to eight months after infection
Publication Details
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2021-01-06
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