New insights into human immune memory from SARS-CoV-2 infection and vaccination

被引:7
作者
Hartley, Gemma E. [1 ]
Edwards, Emily S. J. [1 ]
O'Hehir, Robyn E. [1 ,2 ]
van Zelm, Menno C. [1 ,2 ]
机构
[1] Monash Univ, Cent Clin Sch, Dept Immunol & Pathol, Allergy & Clin Immunol Lab, Melbourne, Vic, Australia
[2] Alfred Hosp, Allergy Asthma & Clin Immunol Serv, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
antibodies; COVID-19; immune memory; memory B cells; memory T cells; SARS-CoV-2; CYTIDINE DEAMINASE AID; B-CELL MEMORY; NEUTRALIZING ANTIBODIES; CHADOX1; NCOV-19; T-CELLS; CORONAVIRUS; IGG; REVEALS; DISEASE; EXPRESSION;
D O I
10.1111/all.15502
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Since early 2020, the world has been embroiled in an ongoing viral pandemic with SARS-CoV-2 and emerging variants resulting in mass morbidity and an estimated 6 million deaths globally. The scientific community pivoted rapidly, providing unique and innovative means to identify infected individuals, technologies to evaluate immune responses to infection and vaccination, and new therapeutic strategies to treat infected individuals. Never before has immunology been so critically at the forefront of combatting a global pandemic. It has now become evident that not just antibody responses, but formation and durability of immune memory cells following vaccination are associated with protection against severe disease from SARS-CoV-2 infection. Furthermore, the emergence of variants of concern (VoC) highlight the need for immunological markers to quantify the protective capacity of Wuhan-based vaccines. Thus, harnessing and modulating the immune response is key to successful vaccination and treatment of disease. We here review the latest knowledge about immune memory generation and durability following natural infection and vaccination, and provide insights into the attributes of immune memory that may protect from emerging variants.
引用
收藏
页码:3553 / 3566
页数:14
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