The clinical features and immune responses of asymptomatic individuals infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have not been well described. We studied 37 asymptomatic individuals in the Wanzhou District who were diagnosed with RT–PCR-confirmed SARS-CoV-2 infections but without any relevant clinical symptoms in the preceding 14 d and during hospitalization. Asymptomatic individuals were admitted to the government-designated Wanzhou People’s Hospital for centralized isolation in accordance with policy1. The median duration of viral shedding in the asymptomatic group was 19 d (interquartile range (IQR), 15–26 d). The asymptomatic group had a significantly longer duration of viral shedding than the symptomatic group (log-rank P = 0.028). The virus-specific IgG levels in the asymptomatic group (median S/CO, 3.4; IQR, 1.6–10.7) were significantly lower (P = 0.005) relative to the symptomatic group (median S/CO, 20.5; IQR, 5.8–38.2) in the acute phase. Of asymptomatic individuals, 93.3% (28/30) and 81.1% (30/37) had reduction in IgG and neutralizing antibody levels, respectively, during the early convalescent phase, as compared to 96.8% (30/31) and 62.2% (23/37) of symptomatic patients. Forty percent of asymptomatic individuals became seronegative and 12.9% of the symptomatic group became negative for IgG in the early convalescent phase. In addition, asymptomatic individuals exhibited lower levels of 18 pro- and anti-inflammatory cytokines. These data suggest that asymptomatic individuals had a weaker immune response to SARS-CoV-2 infection. The reduction in IgG and neutralizing antibody levels in the early convalescent phase might have implications for immunity strategy and serological surveys.
As of May 24, 2020, the coronavirus disease 2019 (COVID-19) pandemic, caused by SARS-CoV-2, has affected more than 5 million people around the world. Most patients with SARS-CoV-2 infections have reportedly had mild to severe respiratory illness with symptoms such as fever, cough and shortness of breath, which might appear 2–14 d after exposure. However, there are other patients who are diagnosed by a positive RT–PCR test but are either asymptomatic or minimally symptomatic2,3,4,5,6. Increasing evidence has shown that asymptomatic individuals can spread the virus efficiently, and the emergence of these silent spreaders of SARS-CoV-2 has caused difficulties in the control of the epidemic2,5. However, our understanding of the clinical features and immune responses of asymptomatic individuals with SARS-CoV-2 infection is limited. Here we describe the epidemiological and clinical characteristics, virus levels and immune responses in 37 asymptomatic individuals.
On February 6, 2020, the National Health Commission of China updated the COVID-19 Prevention and Control Plan (4th edition) for the management of close contacts, emphasizing identification and quarantine of asymptomatic individuals1. To identify asymptomatic individuals, the Wanzhou District Centers for Disease Control and Prevention (CDC) then conducted extensive RT–PCR screening for 2,088 close contacts under quarantine. Individuals with positive RT–PCR results then were screened by point prevalence surveys carried out by the local CDC and symptoms assessments reported by clinicians. Of these, 60 individuals claimed no symptoms in the preceding 14 d, according to local CDC records, and were transferred to a government-designated hospital for centralized isolation. On admission, 17 individuals were excluded for mild or atypical symptoms based on symptoms assessments reported by clinicians; six individuals who developed symptoms 4–17 d after admission were also excluded. Finally, 37 asymptomatic cases, defined as individuals with a positive nucleic acid test result but without any relevant clinical symptoms in the preceding 14 d and during hospitalization, were included in this study. A total of 178 patients with confirmed SARS-CoV-2 infections were identified in the Wanzhou District before April 10, 2020, as tracked by CDC surveillance systems. In this study, the proportion of patients with asymptomatic infections was 20.8% (37/178).
For antibody detection and cytokine measurements, 37 sex-, age-frequency- and comorbidity-matched mild symptomatic patients were selected for comparison with the asymptomatic individuals (Supplementary Table 1). Thirty-seven sex- and age-frequency-matched control individuals from the Wanzhou District with negative RT–PCR results for SARS-CoV-2 were also selected for cytokines comparison.
Of the 37 asymptomatic individuals, the median age was 41 years (range, 8–75 years) and 22 were female. Twenty-eight individuals had a confirmed history of contact with an RT–PCR-confirmed patient with COVID-19, and nine were Wuhan residents or had a travel history to Wuhan before the onset of infection (Supplementary Table 2).
Radiologic and laboratory findings
A complete blood count, blood biochemistry, coagulation function, liver and renal function and infection biomarkers were measured upon admission (Supplementary Table 2) to monitor the potential disease progression, according to the COVID-19 Treatment Guidelines (5th edition) from the National Health Commission of China7. Of the 37 asymptomatic individuals, three had lymphopenia and one had thrombocytopenia. Six individuals had elevated levels of alanine aminotransferase, and 11 had increased C-reactive protein levels.
Upon admission, chest computed tomography (CT) scans showed focal ground-glass opacities in 11 asymptomatic individuals (11/37, 29.7%) and stripe shadows and/or diffuse consolidation in ten individuals (10/37, 27.0%), whereas 16 individuals (16/37, 43.2%) had no abnormalities (Fig. 1). Five individuals developed focal ground-glass opacities or stripe shadows on chest CT within 5 d of hospital admission. There were no pleural effusions, air bronchogram signs or enlarged lymph nodes, which were typical changes seen in critically symptomatic patients8,9,10. Abnormal radiological findings confined to one lung were identified in 66.7% (14/21) of the asymptomatic individuals, whereas 33.3% (7/21) had abnormalities in both lungs.
We compared the RT–PCR cycle threshold (Ct) values of the first positive nasopharyngeal swabs for all 37 asymptomatic individuals and 37 symptomatic patients. The initial Ct values for 37 asymptomatic individuals and 37 symptomatic patients appeared similar (ORF1b 32.8 (IQR, 30.9–35.8) versus 31.7 (IQR, 30.3–35.1), P = 0.336; N 32.6 (IQR, 29.5–34.6) versus 33.5 (IQR, 31.3–37.2), P = 0.126) (Fig. 2a). The median duration of viral shedding, defined as the interval from the first to last positive nasopharyngeal swab, in the asymptomatic individuals was 19 d (IQR, 15–26 d). The shortest observed duration of viral shedding was 6 d, whereas the longest was 45 d. The median duration of viral shedding was 14 d (IQR, 9–22 d) in patients with mild symptoms. The asymptomatic group had a significantly longer duration of viral shedding than the symptomatic group (log-rank P = 0.028) (Fig. 2b). However, measurable virus shedding does not equate with viral infectivity, and further evaluation is needed to determine the respiratory SARS-CoV-2 viral load that is correlated with culturable virus11.
Virus-specific IgG and IgM in asymptomatic individuals
To investigate the acute antibody response to SARS-CoV-2 infection, virus-specific IgG and IgM were measured in serum samples from asymptomatic and symptomatic individuals. In the asymptomatic group, 81.1% (30/37) tested positive for IgG, and 83.8% (31/37) of the symptomatic group tested positive for IgG approximately 3–4 weeks after exposure. Moreover, 62.2% (23/37) of the asymptomatic group were positive for IgM, whereas 78.4% (29/37) of the symptomatic group were IgM positive. Interestingly, IgG levels in the symptomatic group (median S/CO, 20.5; IQR, 5.8–38.2) were significantly higher than those in the asymptomatic group (median S/CO, 3.4; IQR, 1.6–10.7) in the acute phase (the period when the viral RNA can be found in a respiratory specimen) (P = 0.005) (Fig. 3a).
We also followed 37 asymptomatic individuals and 37 symptomatic patients into the early convalescent phase (8 weeks after they were discharged from the hospital). The IgG levels in the symptomatic group were still significantly higher than those in the asymptomatic group in the early convalescent phase (P = 0.002) (Fig. 3b). Surprisingly, the IgG levels in 93.3% (28/30) of the asymptomatic group and 96.8% (30/31) of the symptomatic group declined during the early convalescent phase (Fig. 3c). The median percentage of decrease was 71.1% (range, 32.8–88.8%) for IgG levels in the asymptomatic group, whereas the median percentage of decrease was 76.2% (range, 10.9–96.2%) in the symptomatic group. Using a pseudovirus-based neutralization assay (Methods), we also observed a decrease in neutralizing serum antibodies levels in 81.1% (30/37) of the asymptomatic group and in 62.2% (23/37) of the symptomatic group. The median percentage of decrease was 8.3% (range, 0.5–22.8%) for neutralizing serum antibodies in the asymptomatic group, whereas the median percentage of decrease was 11.7% (range, 2.3–41.1%) in the symptomatic group (Fig. 3d). Moreover, 40.0% (12/30) of asymptomatic individuals, but only 12.9% (4/31) of symptomatic individuals, became seronegative for IgG (Fig. 3e).
Cytokines in asymptomatic individuals
To further elucidate the immune responses associated with SARS-CoV-2 infection, serum cytokines and chemokines levels were compared between the asymptomatic and symptomatic groups. Elevated concentrations of 18 pro- and anti-inflammatory cytokines were observed in the symptomatic group as compared to the asymptomatic group. Of these, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) (P = 3.39 × 10−14), macrophage colony-stimulating factor (M-CSF) (P = 5.08 × 10−13), growth-regulated oncogene-α (GRO-α) (P = 1.5 × 10−10), granulocyte colony-stimulating factor (G-CSF) (P = 2.05 × 10−9) and interleukin 6 (IL-6) (P = 6.33 × 10−9) showed the most significant changes (Fig. 4 and Extended Data Fig. 1). Moreover, the cytokines were further analyzed in the asymptomatic group and the 37 healthy controls. The plasma levels of 32 cytokines were similar between the healthy controls and the asymptomatic individuals. Significantly higher levels of stem cell factor (SCF) (P = 1.48 × 10−9), IL-13 (P = 3.75 × 10−7), IL-12 p40 (P = 7.08 × 10−6) and leukemia inhibitory factor (LIF) (P = 1.33 × 10−3) were found in the asymptomatic group (Extended Data Fig. 2). Collectively, our data show that the asymptomatic individuals had a reduced inflammatory response characterized by low circulating concentrations of cytokines and chemokines.
The clinical features and immune responses of asymptomatic individuals infected with SARS-CoV-2 have not been well described. Of the 178 laboratory-confirmed patients, 37 who never developed any symptoms throughout the disease course were included in this study. Our data showed that 20.8% of these patients had asymptomatic infections. However, this might not be an accurate estimation of the proportion of asymptomatic infections in the general population owing to the fact that asymptomatic infections were identified from those who were at high risk for infection (including close contacts and individuals with a history of travel to Wuhan) and not from a random sample of people. Therefore, the proportion of asymptomatic infections needs to be determined through population screening12. Additionally, the proportion of asymptomatic infections might be even higher as some cases might be missed by RT–PCR testing. Our group has successfully identified seven patients with SARS-CoV-2 infection from 148 cases with negative RT–PCR results and no symptoms by using an antibody test13. Therefore, timely RT–PCR and serological testing should be used in conjunction, which would benefit accurate estimation of the asymptomatic proportion. However, serological testing has limitations, and tests vary in their specificity and sensitivity. Results might also be confounded by previously existing antibodies to SARS-CoV, MERS-CoV or common cold coronaviruses.
To date, the duration of SARS-CoV-2 RNA shedding has not been well characterized. In SARS-CoV, viral RNA was detectable in different specimens, including throat swabs, stool and urine, in more than 30% of patients for as long as 4 weeks after disease onset14. In MERS-CoV infections, viral shedding in respiratory secretions persisted for at least 3 weeks15. Recently, one study of 191 patients with COVID-19 reported that the median duration of viral shedding was 20 d in survivors (range, 8–37 d)16. In another report, the duration of viral shedding in nasopharyngeal aspirates was prolonged up to at least 24 d after symptom onset in 18 patients infected with SARS-CoV-2 in Singapore17. In this study, the median duration of viral shedding in 37 patients with mild symptoms was 14 d, which was shorter than in previous reports. In comparison to symptomatic patients, the asymptomatic group had a significantly longer duration of viral shedding, with a viral shedding time of 19 d. Several factors might contribute to the variation of duration of viral shedding in different studies, including the severity of disease, definition of duration of viral shedding and frequency of specimen collection. Notably, detection of viral RNA does not necessarily mean that infectious virus is present in respiratory specimens, and caution is required when applying virus shedding duration that was calculated based on RT–PCR to assess infection potential.
The strength and duration of immunity after infection are key issues for ‘shield immunity’18 and for informing decisions on how and when to ease physical distancing restrictions19,20. Previous studies have shown that circulating antibodies against SARS-CoV or MERS-CoV last for at least 1 year21,22. Sustained IgG levels were maintained for more than 2 years after SARS-CoV infection23,24. Antibody responses in individuals with laboratory-confirmed MERS-CoV infection lasted for at least 34 months after the outbreak25. Recently, several studies characterizing adaptive immune responses to SARS-CoV-2 infection have reported that most COVID-19 convalescent individuals have detectable neutralizing antibodies, which correlate with the numbers of virus-specific T cells26,27,28,29. In this study, we observed that IgG levels and neutralizing antibodies in a high proportion of individuals who recovered from SARS-CoV-2 infection start to decrease within 2–3 months after infection. In another analysis of the dynamics of neutralizing antibody titers in eight convalescent patients with COVID-19, four patients showed decreased neutralizing antibodies approximately 6–7 weeks after illness onset30. One mathematical model also suggests a short duration of immunity after SARS-CoV-2 infection31. Together, these data might indicate the risks of using COVID-19 ‘immunity passports’ and support the prolongation of public health interventions, including social distancing, hygiene, isolation of high-risk groups and widespread testing. Additional longitudinal serological studies profiling more symptomatic and asymptomatic individuals are urgently needed to determine the duration of antibody-mediated immunity. In addition, low levels of anti-viral IgG in asymptomatic patients, who might be more likely to become seronegative, further support the need for timely serosurvey to study the true infection rate.
Study design and participants
Between January 21 and February 19, 2020, 25 imported symptomatic patients (registered in Wanzhou District), who returned from Wuhan City or Hubei Province, were confirmed with SARS-CoV-2 infection based on a positive RT–PCR test in Wanzhou District. (Wanzhou is the hardest-hit region of Chongqing City, which is a province-level municipality adjacent to Hubei Province.) Up to April 10, 2020, a total of 2,088 individuals, including close contacts of confirmed patients and people returning from Wuhan, were placed under quarantine by the local CDC and tested by RT–PCR. Of these 2,088 individuals, 93 developed symptoms and tested positive for SARS-CoV-2.
On February 6, 2020, the National Health Commission of China updated the COVID-19 Prevention and Control Plan (4th edition) for the management of close contacts, emphasizing the identification and quarantine of asymptomatic individuals. The local CDC then conducted extensive RT–PCR screening of quarantined individuals. Once a case was confirmed positive by RT–PCR, the first prevalence survey was carried out by the local CDC staff. Individuals confirmed to have COVID-19 were asked to provide information, including demography (data of birth, gender and renal disease), preexisting conditions (including history of hypertension, diabetes mellitus, cardiovascular disease, cerebrovascular disease, chronic lung disease, renal disease, chronic hepatopathy and immunodeficiency diseases) and symptoms, as well as screening records for the preceding 14 d (including fever, cough, expectoration, shortness of breath, chill, myalgia, sore throat, runny nose, chest distress, headache, diarrhea, vomiting and nausea). According to the COVID-19 Prevention and Control Plan (4th edition), 60 asymptomatic individuals based on preliminary screening were identified and transferred to a government-designated hospital for centralized isolation. On admission, one-on-one interviews were conducted by clinicians to corroborate the asymptomatic claims. After this screening, 17 individuals were excluded for mild or atypical symptoms. Clinicians conduct daily symptom screening once an individual is admitted to the hospital. Four to 17 days after admission, six of these 43 previously asymptomatic individuals developed symptoms and were re-categorized as symptomatic. Finally, 37 individuals with asymptomatic infections were informed about the study and consented to be included in this study.
It was unclear whether individuals who present with asymptomatic infection might progress to clinical disease during the early phase of the SARS-CoV-2 epidemic in China. Therefore, Chinese clinicians chose to administer interferon-alpha (IFN-α) inhalation, antiviral treatment (ribavirin orally) and supportive treatment (treatment to strengthen immunity, such as thymopentin and Chinese medicine) to avoid possible aggravation, according to the COVID-19 Treatment Guidelines (5th edition) from the National Institutes of Health of China, published on February 8, 2020. The isolation and treatment strategy of asymptomatic infections should be updated according to official guidelines in different countries.
Then, 37 sex-, age-frequency- and comorbidity-matched symptomatic patients were selected for comparison with the asymptomatic individuals (Supplementary Table 1). Thirty-seven sex- and age-frequency-matched controls with negative RT–PCR results for SARS-CoV-2 were also included in this study. Individuals with lung, liver, kidney, cardiovascular, metabolic or immunodeficiency diseases were excluded.
Epidemiologic, demographic, contact and exposure history, clinical presentations, chest CT, laboratory tests, treatment and outcome data were collected from inpatient medical records. Laboratory data collected for each patient included complete blood count, coagulation profile, serum biochemical tests (including renal and liver function, electrolytes, lactate dehydrogenase and creatine kinase), serum ferritin and biomarkers of infection. Chest CT scans were done for all inpatients.
To identify SARS-CoV-2 infection, nasopharyngeal swabs were collected at least twice and tested by RT–PCR. RNA from all samples was isolated within 24 h. Viral RNA samples were extracted according to manufacturer instructions using the Nucleotide Acid Extraction Kit (DAAN Gene, registration no. 20170583), which based on an automated magnetic bead purification procedure. A commercial RT–PCR kit (DAAN Gene, registration no. 20203400063) was used for testing samples for SARS-CoV-2. Briefly, two target genes, including open reading frame1ab (ORF1ab) and nucleocapsid protein (N), were simultaneously amplified and tested during RT–PCR. Primers of RT–PCR testing for SARS-CoV-2 were according to the recommendation by the Chinese CDC (ORF1ab forward: CCCTGTGGGTTTTACACTTAA, ORF1ab reverse: ACGATTGTGCATCAGCT GA, ORF1ab probe: 5′-CCGTCTGCGGTATGTGGAAAGGTTATGG-3′ (FAM dye labeled); N forward: GGGGAACTTCTCCTGCTAGAAT, N reverse: CAGACATT.
TTGCTCTCAAGCTG, N probe: 5′-TTGCTGCTGCTTGACAGATT-3′ (VIC dye labeled)). PCR cycling: 50 °C for 15 min, 95 °C for 15 min, 45 cycles containing 94 °C for 15 s, 55 °C for 45 s (fluorescence collection).
Ct values less than 37 and greater than 40 were defined as positive and negative, respectively, for both genes. Samples with Ct values from 37 to 40 were defined as inconclusive, and a second test was needed. Starting 1 week after admission, nasopharyngeal samples were tested by RT–PCR every 2–3 d for the remainder of the hospitalization period. Patients with one positive RT–PCR result were defined as patients with SARS-CoV-2 infection. Patients with two consecutive negative RT–PCR results were defined as SARS-CoV-2 negative.
A confirmed case of COVID-19 was defined as an individual with nasopharyngeal swabs that were positive for SARS-CoV-2, using laboratory-based PCR. The symptomatic patients were defined as patients with laboratory-confirmed COVID-19 with symptoms such as fever, cough, sore throat and sputum. An asymptomatic case was defined as an individual with a positive nucleic acid test result but without any relevant clinical symptoms in the preceding 14 d and during hospitalization. A close contact was defined as (1) anyone who had been within approximately 6 feet (2 meters) of a person infected with SARS-CoV-2 for longer than 10 min and (2) those who had direct contact with the infectious secretions of a COVID-19 patient. Close contact can occur while caring for, living with, visiting or sharing a healthcare waiting area or room with patients with COVID-19. The duration of shedding was calculated as the number of days from the first positive nasopharyngeal sample to the last positive sample based on RT–PCR testing. The last positive sample was followed by a negative RT–PCR result on two sequential tests.
Detection of IgG and IgM against SARS-CoV-2
IgG and IgM against SARS-CoV-2 were detected in plasma samples using magnetic chemiluminescence enzyme immunoassay kits (Bioscience), according to the manufacturer’s instructions. Briefly, recombinant antigens containing the nucleoprotein and a peptide (LQPELDSFKEELDKYFKNHTSPDVD) from the spike protein of SARS-CoV-2 were immobilized on magnetic particles.
Neutralization detection using pseudovirus neutralizaion assay
A codon-optimized spike (S) that lacked the C-terminal 19 amino acids was used to generate a luciferase-expressing pseudovirus. The SARS-CoV-2 pseudovirus neutralization assay was carried out on 293T cells expressing ACE2 in a 96-well plate. Paired dilute sera (1:600) from an individual (one serum sample from the acute phase and another serum sample from the convalescent phase) were obtained, equal volumes of SARS-CoV-2 pseudovirus were added and the plates were pre-incubated at 37 °C for 1 h. Then, 293T cells expressing ACE2 were incubated with 100 μl of sera-pseudovirus mixture for 24 h. Three days after infection, the cells were lysed with 30 μl of lysis buffer (Promega) to measure the pseudoviral transduction. Relative luminescence units of luciferase activity were detected using the Luciferase Assay Kit (Promega), according to the manufacturer’s instructions. Experiments were repeated twice. The luciferase activity was determined by GloMax Microplate Luminometer (Promega). The neutralization rate (%) was calculated as following:
The sera of patients with laboratory-confirmed SARS-CoV-2 infections (asymptomatic group n = 37 and symptomatic group n = 37) were collected as early as possible during hospitalization. The sera of healthy individuals (n = 37) were included as control groups. The concentrations of 48 cytokines and chemokines were measured using the Bio-Plex Human Cytokine Screening Panel (48-Plex no. 12007283, Bio-Rad) on a Luminex 200 (Luminex Multiplexing Instrument, Merck Millipore) following the manufacturer’s instructions. The 48 cytokines screening panel includes: fibroblast growth factor (FGF), eotaxin, granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), interferon-gamma (IFN-γ), interleukin-1 beta (IL-1β), interleukin 1 receptor antagonist (IL-1RA), interleukin 1 alpha (IL-1α), interleukin-2 receptor-alpha (IL-2Rα), interleukin-3 (IL-3), interleukin-12 p40 (IL-12 (p40)), interleukin-16 (IL-16), interleukin-2 (IL-2), interleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-6 (IL-6), interleukin-7 (IL-7), interleukin-8 (IL-8), interleukin-9 (IL-9), growth-regulated oncogene-alpha (GRO-α), hepatocyte growth factor (HGF), interferon alpha-2 (IFN-α2), leukemia inhibitory factor (LIF), monocyte-chemotactic protein 3 (MCP-3), interleukin-10 (IL-10), interleukin-12 p70 (IL-12 (p70)), interleukin-13 (IL-13), interleukin-15 (IL-15), interleukin-17A (IL-17A), interferon gamma-inducible protein (IP-10), monocyte chemoattractant protein-1 (MCP-1), monokine induced by gamma interferon (MIG), beta-nerve growth factor (β-NGF), stem cell factor (SCF), stem cell growth factor-beta (SCGF-β), stromal cell-derived factor 1 (SDF-1α), macrophage inflammatory protein-1 alpha (MIP-1α), macrophage inflammatory protein-1 beta (MIP-1β), platelet-derived growth factor-BB (PDGF-BB), regulated upon activation, normal T cell expressed and presumably secreted (RANTES), tumor necrosis factor alpha (TNF-α), vascular endothelial growth factor (VEGF), cutaneous T-cell-attracting chemokine (CTACK), macrophage migration inhibitory factor (MIF), TNF-related apoptosis-inducing ligand (TRAIL), interleukin-18 (IL-18), macrophage colony-stimulating factor (M-CSF) and tumor necrosis factor-beta (TNF-β).
All continuous characteristics are described as the medians (IQRs), and categorical characteristics are described as numbers (%). Significant differences of continuous characteristics between asymptomatic and symptomatic and asymptomatic and healthy control groups were determined by the Mann–Whitney U test. Categorical characteristics comparison was performed with Fisher’s exact test. P value cutoffs of 0.05 for antibody and 0.001 for cytokines indicated significance. The Kaplan–Meier method was used to analyze the duration of viral shedding in the symptomatic and asymptomatic groups. Statistical analyses were performed using R software (version 3.6.0).
The study was approved by the Ethics Commission of Chongqing Medical University (reference no. 2020004). Written informed consent for participation in this study was obtained from all adult participants or guardians on behalf of the children enrolled in this study.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Raw data in this study are provided in the Supplementary Dataset. Additional supporting data are available from the corresponding authors upon reasonable request. All requests for raw and analyzed data and materials will be reviewed by the corresponding authors to verify whether the request is subject to any intellectual property or confidentiality obligations. Source data are provided with this paper.
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We thank C.-Y. Yang and B. Anderson for critical review of the manuscript. This study received the following funding: the National Science and Technology Major Project (2017ZX10202203); the Emergency Project from the Science & Technology Commission of Chongqing; and the National Natural Science Foundation of China (grant nos. 81871656 and 8181101099). We acknowledge all patients involved in the study.
The authors declare no competing interests.
Peer review information Saheli Sadanand was the primary editor on this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended Data Fig. 1 Comparison of serum cytokine/chemokine concentrations between the asymptomatic and symptomatic groups.
Samples from asymptomatic individuals (n = 37) and symptomatic patients (n = 37) were collected for assays measuring the concentrations of 48 cytokines and chemokines. 25 cytokines or chemokines were similar between asymptomatic individuals and symptomatic patients. 5 cytokines or chemokines were significantly higher in asymptomatic individuals than in symptomatic patients. The boxplots show medians (middle line), first and third quartiles (boxes), while the whiskers show 1.5× the interquartile range (IQR) above and below the box. Unpaired, two-sided Mann-Whitney U test p values are depicted in plots, and the significant p value cut-off was set to 0.001. Source data
Extended Data Fig. 2 Comparison of serum cytokine and chemokine concentrations between the asymptomatic and healthy groups.
Samples from healthy controls (n = 37) and asymptomatic individuals (n = 37) were collected for assays measuring the concentrations of 48 cytokines and chemokines. A. Thirty-two cytokines or chemokines were similar between healthy controls and asymptomatic individuals. B. Sixteen cytokines or chemokines were significantly different between healthy controls and asymptomatic individuals. The boxplots show medians (middle line), first and third quartiles (boxes), while the whiskers show 1.5× the interquartile range (IQR) above and below the box. Unpaired, two-sided Mann-Whitney U test p values are depicted in plots, and the significant p value cut-off was set to 0.001. Source data
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Long, QX., Tang, XJ., Shi, QL. et al. Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections. Nat Med 26, 1200–1204 (2020). https://doi.org/10.1038/s41591-020-0965-6
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