The SARS-CoV-2 virus infects humans via droplets, and to some extent, aerosols1. In symptomatic adults, the disease typically presents after 2–14 days of incubation as a respiratory illness with fever, cough, headache, myalgia and in some cases intestinal symptoms2. A growing number of studies are pointing toward asymptomatic infection in a significant fraction of individuals3, and as many as half of all transmission events occur from presymptomatic and asymptomatic individuals4.

In this Perspective, I discuss what we know about the immune response to SARS-CoV-2 infection and how this might explain different disease presentations and disease severity by considering known immunological differences between the groups that are most commonly affected.

COVID-19 disease courses

Mild and severe acute COVID-19

It is clear that the outcome of infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) varies broadly, with the majority of young individuals experiencing mild disease5. Also, sex is an important; men are over-represented among patients with severe disease, presumably due to differences in the elicited immune responses6. Comorbidities such as obesity, hypertensive disease, chronic obstructive pulmonary disease and cardiovascular disease are all associated with severe COVID-19 disease2. Higher SARS-CoV-2 copy numbers at diagnosis have been reported in patients with severe COVID-19 than in those with mild COVID-19 (ref. 7). Smoking is yet another risk factor: cigarette smoke induces expression of angiotensin-converting enzyme 2 (ACE2), which allows SARS-CoV-2 to enter cells, and could possibly influence viral invasion8 beyond its negative effects on overall lung function.

Despite the increased risk of severe disease with increased age, a minor subset of young and middle-aged individuals present with severe COVID-19 disease characterized by poor oxygen saturation and massive inflammatory responses in the lung. Such cases need urgent management and intensive care, and several studies have attempted to unravel the mediators of such hyperinflammatory disease presentation9,10,11,12,13.


Apart from the differences in severity among patients with acute COVID-19, it is now clear that a number of other outcomes are possible after an initial infection with SARS-CoV-2. After a long period of intensive care and mechanical ventilation, general anesthesia and severe illness, it is not surprising that long rehabilitation periods are needed14. However, it is now also clear that some individuals with milder initial symptoms of COVID-19 can suffer from variable and debilitating symptoms for many months after the initial infection15,16. This condition is popularly referred to as long COVID. An exact definition is lacking, but typically symptoms with a duration >2 months are considered long COVID. The condition involves a range of symptoms such as persistent fatigue, myalgia, autonomic dysregulation manifested as postural orthostatic tachycardia syndrome, abnormal thermoregulation, intestinal disturbances and skin manifestations17. This post-COVID syndrome bears resemblance to postinfectious syndromes that followed outbreaks of chikungunya18 and Ebola19, for example, and selected symptoms overlap with myalgic encephalomyelitis, a disease that is also often triggered by infection and immune activation20 and manifests as a dysregulated autonomic nervous system and perturbed immune parameters21. More research is needed to understand the pathogenesis of all of these postinfectious conditions, and long COVID offers a unique opportunity to perform such studies in larger numbers of individuals, all infected by the same virus during a limited time frame.

Multisystem inflammatory syndrome associated with COVID-19

Another rare and serious postinfectious condition that can occur 2–6 weeks after SARS-CoV-2 infection is the multisystem inflammatory syndrome associated with COVID-19, first described in children (MIS-C)22,23,24, and more recently in young adults (MIS-A)25. This hyperinflammatory syndrome shares clinical features with Kawasaki disease26, but affects children who are older than the typical patient with Kawasaki disease and who more often present with intestinal involvement and myocardial failure and shock. There is also significant clinical overlap in presentation with toxic shock syndrome22 or septic shock. Subgroups of children affected by MIS-C are being described27, and optimal management is being worked out by collaborative networks of pediatricians. Most MIS-C patients are treated with strong immunomodulatory regimens such as high-dose steroids, intravenous immunoglobulins and anti-cytokine therapies coupled with anti-coagulation to counter the microangiopathy and activation of both complement and coagulation cascades during the hyperinflammatory disease phase28,29. The pathogenesis of MIS-C is unknown, but a delay of 2–6 weeks from initial SARS-CoV-2 infection indicates a role for adaptive immune responses and specific autoantibodies have been proposed30,31.

Viral recognition and innate immune responses

Viral entry

SARs-CoV-2 infects cells by attaching to the principal viral entry receptor, ACE2 (ref. 32). The expression of this receptor has been reported in single-cell messenger-RNA-sequencing data on epithelial cells in the oral mucosa33, liver, kidney, intestine and heart34, and at the protein level in alveolar epithelial cells35, although the tissue distribution of protein expression differs to some extent36. Several reports have shown abundant expression of ACE2 in the intestinal epithelium leading to viral shedding via feces37, while ACE2 does not seem to be expressed by cells of the immune system38.

Innate immune responses

SARS-CoV-2, like the related SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV), is a single-stranded RNA virus. After entering a target cell, the virus is recognized by pattern recognition receptors such as Toll-like receptors 3, 7, 8 and 9 and viral-infection sensors RIG-I and MDA5 (ref. 39), and viral recognition induces the type I interferon (IFN) response program and IFN-stimulated genes40 (Fig. 1a). The TLR3 response triggers transcription of the NLR family pyrin domain containing 3 (NLRP3) gene, which together with other cellular responses to viral infection—such as the formation of reactive oxidative species, calcium flux from cytoplasmic storages, protein aggregation and the release of danger-associated patterns—contributes to the activation of the NLRP3 inflamasome41 and likely other inflammasome complexes. The NLRP3 inflammasome induces caspase-1-dependent cleavage and release of key proinflammatory cytokines interleukin-1β (IL-1β) and IL-18, and triggers gasdermin D-mediated pyroptotic cell death. The extent of NLRP3 activation correlates with COVID-19 disease severity42 (Fig. 1b). As a result of pyroptotic cell death, the enzyme lactate dehydrogenase (LDH) is released. Elevated LDH levels have been observed in the blood of patients with COVID-19, and levels of this enzyme correlate with disease severity2. Together, these data suggest that inflammasome activation is an important feature of COVID-19 (ref. 43) (Fig. 1b). This pathway also triggers the coagulation cascade, for example via the extracellular release of gasdermin D44, and coagulopathy and severe thrombotic events are common in patients with severe COVID-19 (ref. 45). A similar activation of the coagulation cascade and elevated LDH levels are also seen in patients with MIS-C22, but not in patients with long COVID46, indicating differences in the underlying pathogenesis.

Fig. 1: Coronavirus recognition and immune response.
figure 1

a, SARS-CoV-2 viruses bind to the ACE2 receptor for cell entry. Viral RNA is recognized by TLR3, which triggers transcriptional responses and cytoplasmic changes that activate the NLRP3 inflammasome. This leads to cleavage of precursor IL-1β (pro-IL-1β), pro-IL-18 and gasdermin D, allowing secretion of IL-1β and IL-18. These changes collectively induce pyroptosis, inflammation and coagulopathy. b, Secreted IL-18 together with IL-12 from myeloid cells stimulate TH1 immunity and natural killer cells to secrete IFN-γ. c, A key feature of coronaviruses (MERS-CoV, SARS-CoV) is a capability to inhibit and delay the type I IFN response, leading to increased viral replication and severe immunopathology.

A characteristic feature of SARS-CoV and MERS-CoV viruses is their ability to inhibit and delay the induction of type I IFN by infected cells, which contributes to the immunopathology associated with such infections47,48. Also, SARS-CoV-2 is able to inhibit the type I IFN responses in infected cells, leading to delayed or overall suppressed type I IFN responses49,50. This allows the virus to replicate and induce more tissue damage, and triggers a more exuberant immune response as the immune system struggles to limit viral replication and to manage dying and dead cells. Immune pathology continues as inflammatory cells flow into the lung and produce large amounts of proinflammatory cytokines, further escalating the situation (Fig. 1c). Such imbalanced immune responses, caused in part by the impaired early type I IFN responses, are the most likely determinant of the overall severity of acute COVID-19 (refs. 50,51,52,53). This is further emphasized by recent results from the COVID Human Genetic Effort54 (, which found that inborn errors in the type I IFN pathway55, or the presence of neutralizing autoantibodies to type I IFNs56, were strongly over-represented among individuals who developed life-threatening COVID-19. Whether imbalanced or impaired innate responses also contribute to the development of other disease manifestations such as MIS-C and long COVID remains to be determined.

Adaptive immune responses

Serological tests for SARS-CoV-2 have been the subject of much discussion and conflicting results during the course of this pandemic so far. However, with time it has become apparent that the adaptive immune responses induced by SARS-CoV-2 infection largely follow the expected patterns based on what is known from other comparable viral infections, with >90% of infected individuals seroconverting a few weeks after initial infection57,58. Presence of anti-spike IgG antibodies were associated with protection from reinfection in a UK cohort of health-care workers at high risk of exposure59.

T cell responses to the SARS-CoV-2 spike protein correlate with B cell responses to the same protein and are detectable in nearly all convalescent patients with COVID-19 (ref. 60). T cell reactivity to SARS-CoV-2 can also be detected in unexposed individuals, presumably due to cross-reactive immunity to common-cold coronaviruses60 or to other antigens, as has been shown for other virus-specific T cells61. Another study has reported SARS-CoV-2-reactive T cells in patients who survived the SARS epidemic in 2003, but also in unexposed individuals; interestingly, such responses preferentially targeted epitopes different from the ones in convalescent patients with COVID-19, and were not homologous with common-cold coronaviruses, but conserved among animal coronaviruses62.

Antibody-dependent enhancement (ADE), a phenomenon that has been described for infections with viruses such as dengue63, has been proposed as a possible mechanism of severe COVID-19. ADE occurs when antibodies target a virus without neutralizing it, for example if the antibody is raised against a different serotype of the virus or when the antibody fails to block viral entry. Then, the antibody might facilitate Fc-receptor-mediated endocytosis of the virus and enhanced viral replication, and massive inflammatory responses. This has been described to occur for MERS64, but no clear evidence of ADE as a cause of severe SARS-CoV-2 infection has been communicated. Reinfections have been reported, and in a few instances, the second infection was more severe than the first, but serological responses suggest that patients never seroconverted after initial infection and ADE is a less likely cause of a more severe second infection65.

The role of pre-existing immunity to common-cold coronaviruses is another possible determinant of COVID-19 disease severity66. T cell reactivity is found in unexposed individuals and has been linked to prior exposures to common-cold coronaviruses67. Also, IgG that is specific to SARS-CoV-2 spike protein has been found in unexposed individuals, particularly in children and young adults, and some of these had neutralizing activity against SARS-CoV-2, indicating a potentially protective effect against severe COVID-19 (ref. 68). Another study also identified such antibodies but found no evidence for a protective effect against COVID-19 (ref. 69). Cross-reactive antibodies are also more frequently found in serum samples collected in sub-Saharan Africa prior to the COVID-19 pandemic70, indicating a possible explanation for the surprisingly low number of severe COVID-19 cases seen on this continent. Whether there is a role for cross-reactive antibodies or T cells, or the absence of such features, in determining other disease manifestations, such as MIS-C or long COVID, remains to be seen. Children who develop MIS-C have detectable IgG responses without obvious differences from convalescent children without MIS-C29,71,72, although one study indicated subtle IgG-subclass and functional differences between children with MIS-C and those without MIS-C73.

Known immunological differences between high- and low-risk individuals

The risk of developing severe COVID-19 increases steeply above age 70, and also with the severity of obesity and other risk factors. Men have a much greater risk of severe acute COVID-19 than women, whereas women are over-represented among patients who develop long COVID15. The infection differs from many other respiratory infections in that children are seemingly able to cope, even in the very first years of life, without developing severe respiratory disease except in a few rare cases. The known immunological differences between young and old people and between men and women should help us further unravel the immunological mechanisms behind disease presentation and severity.

Sex differences

As mentioned above, type I IFN responses are critical determinants of disease severity during acute SARS-CoV-2 infection, and the virus has developed methods for subverting these responses. Women elicit stronger type I IFN responses upon stimulation with TLR7 ligands74 and develop stronger vaccine responses75, but also more side effects, and have better survival rates for a number of acute infections than do men76. These sex differences are seen even in boys and girls before puberty—pointing towards genetic, rather than hormonal, differences. It is worth noting that a common sensor of viruses, TLR7, is expressed on the X chromosome, providing a possible difference in gene-dosage effect between men and women77. Interestingly, the neutralizing autoantibodies to type I IFN found in patients with severe COVID-19 were much more abundant in men than in women, but the reasons for this are elusive56. Immune-response differences have also been reported between male and female patients with COVID-19 (ref. 6), and collectively these sex differences could explain the overall susceptibility of male patients to developing severe acute COVID-19. MIS-C is quite evenly distributed between boys and girls22, whereas long COVID is more prevalent in female patients15,16. It is also important to consider whether social factors and differing exposure play a part in sex differences.

Age differences

If type I IFN responses were the sole determinants of COVID-19 severity, one would expect young children to be highly susceptible because both newborn and young children produce lower amounts of type I IFN upon stimulation through various viral-sensing pathways78. The low risk of severe SARS-CoV-2 disease in young children also differs from that of other respiratory viral infections like the flu79, and points toward other protective mechanisms in young children. The immune systems of young children are accustomed to facing novel challenges, whereas older individuals rely more on memory responses. The thymus decreases its output of naive T cells and involutes at a rate of about 3% per year, and some data indicate more rapid involution in boys than in girls80. Cross-reactive antibodies to common-cold coronaviruses are one possible explanation; another possibility is that constitutive differences in immune system states between young and old people are of importance. One example could be the skewing of T cells from T helper type 1 (TH1) toward more TH2 in young children81 (Fig. 2).

Fig. 2: Immune-system parameters associated with obesity, aging and severe COVID-19.
figure 2

The gradient illustrates the risk of developing severe COVID-19 in relation to known immune system changes with age (x axis) and obesity (y axis).

Disease severity in COVID-19 also correlates with neutrophil-to-lymphocyte ratio (NLR)82, a metric reflecting immune-cell composition that is frequently studied across populations and disease conditions as a surrogate marker of systemic inflammation. The NLR ratio positively correlates with advancing age83 and with the degree of obesity, especially in the context of metabolic syndromes and type 2 diabetes84. As such, the NLR ratio is indicative of low-grade inflammation, ‘inflammaging’ and obesity-associated inflammation, and is a poor prognostic factor in COVID-19 (Fig. 2). This observation indicates that individuals with such underlying immune-system conditions either fail to develop productive antiviral immune responses or are more prone to develop uncontrolled, exuberant responses upon infection, leading to hyperinflammation and acute respiratory distress syndrome, characteristic of severe COVID-19 (Fig. 2). Older individuals typically produce weaker type I IFN responses upon viral infection, which further worsen the situation85. Also, additional markers of inflammaging and obesity-associated inflammation have been shown to be predictive of a severe COVID-19 course, such as NLRP3 activation43, IL-6, IL-12 and IL-1β secretion86 and danger-associated molecular patterns, including high mobility group box 1 (HMGB1)87 (Fig. 2).


Since the beginning of the pandemic, there have been grave concerns over the risk of developing severe COVID-19 for individuals with immunodeficiencies or those taking immunosuppressive therapies. One systematic review found no statistically significant increased risk of severe COVID-19 in immunosuppressed patients88, but other studies have shown an increased risk for patients with solid-organ transplants and some patients with cancer89. Patients with cancer treated with checkpoint inhibitors are at particularly high risk of severe COVID-19, according to another recent report90. It is important to note that type and degree of immunosuppression likely varies substantially among heterogeneous patient groups, and more detailed subset analyses are needed. This is also highlighted by an Italian study of patients with different forms of primary antibody deficiencies, in which patients with combined variable immunodeficiency, often associated with low-grade inflammation, developed severe COVID-19, while patients with similarly low antibody levels due to other forms of inborn errors of immunity generally experienced milder course of disease91.

Future directions

In summary, COVID-19 can develop into a life-threatening hyperinflammatory disease in rare cases, and global efforts are ongoing to better understand productive immune responses against the SARS-CoV-2 virus and the immunopathological mechanisms underlying severe disease. At the same time, additional disease outcomes, such as MIS-C, MIS-A and long COVID, are becoming increasingly known. By considering known differences between high- and low-risk individuals for each of these conditions, we will be able to design optimal studies contrasting such patient groups and their immune responses. The origin of the different disease trajectories upon SARS-CoV-2 infection can likely be traced back to the early stages of infection, as illustrated by the essential role for type I IFN responses during acute COVID. With this Perspective, I hope to open up a discussion on the different disease manifestations, their shared and distinguishing features and affected populations and immunological features.