COVID-19 has led to a global pandemic, but the long-term immunological effects of the infection are only partially understood. A new study now provides important new clues by describing the transcriptional and epigenetic processes behind the immune memory of both adaptive and innate immune cells in individuals who have recovered from COVID-19.
Initially emerging in China in December 2019, the coronavirus disease COVID-19 caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has become a major health crisis, with high morbidity and mortality, especially among the elderly and people with various comorbidities1. Much has been learned in the past year regarding pathophysiology of the disease, in which immune-based mechanisms play a major role not only for protection, but also for immunopathology. While novel therapies have been developed based on immunomodulatory drugs (such as dexamethasone or IL-6 blockers), vaccination remains the most effective approach to blocking the spread of the virus and alleviate the consequences of the pandemic.
Several successful vaccines have been already developed based on various technological platforms, including mRNA technology, adenovirus platforms, recombinant proteins or inactivated viruses. While several of these have proved to be effective in short-term phase 3 trials2, little is known regarding the duration of their effects and the precise immune correlates of protection mediating the protection. It is therefore crucial to understand in detail the immunological memory processes inducing protection against the virus after natural COVID-19 infection. We would be thus able to employ more rationally the available vaccines and even design and develop the next generation of vaccines with improved and longer protection against infection. In this issue of Nature Cell Biology, You et al. now make one important step in that direction by describing the transcriptional and epigenetic processes behind the long-term memory of immune cells in individuals who have recovered from COVID-193. By using cutting-edge single-cell sequencing technology, the authors describe the transcriptional modules, the regulatory nodes at the level of transcription factors, and the chromatin accessibility in various immune cell types after COVID-19 recovery.
The first line of evidence provided by You and colleagues addresses the mechanisms of adaptive immune memory at the level of B cells and T cells (Fig. 1). Lymphocytes are crucial components of the long-term protection induced either by natural infection or by vaccination; while their role as correlates of protection against COVID-19 has not been formally demonstrated, it is widely assumed that they mediate the protection induced by natural infection or vaccines4,5. First, You et al. identified important differences in the developmental processes in B lymphocytes from COVID-19 convalescent individuals compared to healthy volunteers, based on differential B-cell lineage trajectories in chromatin accessibility. Second, the authors also identified crucial differences in transcription factor (TF) regulators, with the NF-κB subunits RELA and RELB being enriched in B cells of healthy volunteers, while activator protein 1 (AP-1) transcription factors FOS and JUN being higher in naïve, memory and plasma B cells of COVID-19 convalescent individuals. Based on the integrated timing of TF activity, the authors concluded that TFs expressed in B cells of healthy individuals promote maintenance and homeostasis, while inducing B-cell activation, differentiation, and IgG class switch recombination in COVID-19 convalescent individuals. Third, You and colleagues described the transcriptional and chromatin landscape of T cells after infection with SARS-CoV-2. In contrast to healthy volunteers, COVID-19 convalescent individuals displayed enhanced effector and memory CD8+ cells, which is not surprising considering their role in antiviral immunity. The authors also described the TF regulators in CD8+ cells, which again comprise the AP-1 factors FOS and JUNB, supported by earlier literature6. Memory commitment on the other hand involves Kruppel-Like Factors 2 and 3. Interestingly, T-cell receptor clonality analysis showed a very substantial expansion of CD8+ clones, while CD4+ T cells displayed diverse repertoire with minimal expansion. Altogether, the transcriptional and epigenetic analysis of lymphocytes from COVID-19 convalescent individuals argues for an important role of B cells and CD8+ T cells in mediating memory responses after natural infection, and it is rational to explore these pathways for improvement of vaccination efficacy.
While memory responses in B and T lymphocytes are expected after a viral infection, a more surprising finding of You and colleagues relates to the identification of long-term adaptive changes in monocytes as well. Adaptive characteristics in the myeloid cell lineage have been recently described after certain infections, and especially vaccinations, resulting in improved responses (cytokine and ROS production, phagocytosis, microbial killing) of innate immune cells upon stimulation with heterologous stimuli. This de facto non-specific immunological memory of myeloid cells is mediated by transcriptional and epigenetic rewiring, and has been termed ‘trained immunity’7. Interestingly, the authors identified a trained immunity phenotypic program induced by SARS-CoV-2 infection in both CD14+ and CD16+ monocytes from COVID-19 convalescent individuals (Fig. 1). This program included increased chromatin accessibility in monocytes after recovery from COVID-19 for both IL1B and chemokine genes, which are well known to be both important for trained immunity8 and strongly activated in COVID-199. Increased chromatin accessibility was associated with higher production of these cytokines after stimulation, further confirming a trained phenotype in monocytes in post-COVID19 individuals.
The identification of trained monocytes after recovery from SARS-CoV-2 is important at several levels. On one hand, this provides a more comprehensive understanding of the changes in immune responses after infection with COVID-19, demonstrating long-term adaptation not only in lymphocytes but also in myeloid cells. On the other hand, the discovery of these processes is also exciting for understanding the potential consequences of the disease. It is tempting to speculate that induction of trained immunity could contribute to the long-term protection against reinfection, and that this needs to be considered for the development of future vaccines. However, such enhanced responsiveness of myeloid cells may lead in some individuals to adverse hyperactivation, such as in multisystem inflammatory syndromes in adults (MIS-A) or children (MIS-C), or even in people with long-term symptoms after COVID10.
All in all, the study describes for the first time important regulatory nodes of memory in adaptive immunity and opens the door to a new field in COVID-19 research showing long term-regulation and trained immunity in myeloid cells of convalescent individuals. Future studies are warranted to explore these processes in more depth, and larger studies are needed to assess potential differences between patients with mild, moderate, severe COVID-19 or convalescent individuals. Systems approaches based on multi-omics data will be necessary to reveal the underlying molecular circuits of immune response to viral infection, longitudinal studies will be needed to understand the kinetics of these processes, and clinical and translational studies should be done to understand the potential use of this knowledge for the treatment of late complications of COVID-19, and even improve vaccination. Only with such future studies the potential of these discoveries will be fulfilled.
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M.G.N. was supported by an ERC Advanced Grant (#833247) and a Spinoza Grant from the Netherlands Organization for Scientific Research. Y.L. was supported by an ERC Starting Grant (#948207) and the Radboud University Medical Centre Hypatia Grant (2018).
The authors declare no competing interests.
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Netea, M.G., Li, Y. Immune memory in individuals with COVID-19. Nat Cell Biol 23, 582–584 (2021). https://doi.org/10.1038/s41556-021-00689-8