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. 2021 May 12:jiab255. doi: 10.1093/infdis/jiab255

Persistence of Antibody and Cellular Immune Responses in COVID-19 patients over Nine Months after Infection

Lin Yao 1,#, Guo-Lin Wang 1,#, Yuan Shen 2,#, Zhuang-Ye Wang 3,#, Bing-Dong Zhan 4,#, Li-Jun Duan 1, Bing Lu 2, Chao Shi 2, Yu-Meng Gao 2, Hong-Hong Peng 2, Guo-Qiang Wang 3, Dong-Mei Wang 3, Ming-Dong Jiang 3, Guo-Ping Cao 4, Mai-Juan Ma 1,
PMCID: PMC8243600  PMID: 33978754

Abstract

Background

The duration of humoral and T and cell response after the infection of SARS-CoV-2 remains unclear.

Methods

We performed a cross-sectional study to assess the virus-specific antibody and memory T and B cell responses in COVID-19 patients up to 343 days after infection. Neutralizing antibodies and antibodies against the receptor-binding domain, spike, and nucleoprotein of SARS-CoV-2 were measured. Virus-specific memory T and B cell responses were analyzed.

Results

We enrolled 59 COVID-19 patients, including 38 moderate, 16 mild, and five asymptomatic patients; 31 (52.5%) were men, and 28 (47.5%) were women. The median age was 41 (interquartile range [IQR]: 30–55). The median day from symptom onset to enrollment was 317 days (range 257 to 343 days). We found that approximately 90% of patients still have detectable IgG antibodies against spike and nucleocapsid proteins and neutralizing antibodies against pseudovirus, whereas ~60% of patients had detectable IgG antibodies against receptor binding domain and surrogate virus-neutralizing antibodies. SARS-CoV-2-specific IgG + memory B cell and IFN-γ secreting T cell responses were detectable in over 70% of patients.

Conclusions

SARS-CoV-2-specific immune memory response persists in most patients nearly one year after infection, which provides a promising sign for prevention from reinfection and vaccination strategy.

Keywords: SARS-CoV-2, neutralizing antibody, memory T cell, memory B cell, persistence

Supplementary Material

jiab255_suppl_Supplementary_Materials

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

jiab255_suppl_Supplementary_Materials

Articles from The Journal of Infectious Diseases are provided here courtesy of Oxford University Press

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