Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the rapidly unfolding coronavirus disease 2019 (COVID-19) pandemic1,2. Clinical manifestations of COVID-19 vary, ranging from asymptomatic infection to respiratory failure. The mechanisms that determine such variable outcomes remain unresolved. Here we investigated CD4+ T cells that are reactive against the spike glycoprotein of SARS-CoV-2 in the peripheral blood of patients with COVID-19 and SARS-CoV-2-unexposed healthy donors. We detected spike-reactive CD4+ T cells not only in 83% of patients with COVID-19 but also in 35% of healthy donors. Spike-reactive CD4+ T cells in healthy donors were primarily active against C-terminal epitopes in the spike protein, which show a higher homology to spike glycoproteins of human endemic coronaviruses, compared with N-terminal epitopes. Spike-protein-reactive T cell lines generated from SARS-CoV-2-naive healthy donors responded similarly to the C-terminal region of the spike proteins of the human endemic coronaviruses 229E and OC43, as well as that of SARS-CoV-2. This results indicate that spike-protein cross-reactive T cells are present, which were probably generated during previous encounters with endemic coronaviruses. The effect of pre-existing SARS-CoV-2 cross-reactive T cells on clinical outcomes remains to be determined in larger cohorts. However, the presence of spike-protein cross-reactive T cells in a considerable fraction of the general population may affect the dynamics of the current pandemic, and has important implications for the design and analysis of upcoming trials investigating COVID-19 vaccines.
The COVID-19 pandemic poses a threat to public health and the global economy as the number of cases and COVID-19-related deaths increases worldwide1,2. COVID-19 is routinely diagnosed by the detection of SARS-CoV-2 RNA in nasopharyngeal swabs using PCR3, the detection of which is reliable during the acute phase of COVID-194,5. However, the limited availability of tests and the preferential testing of patients with symptoms has probably led to a marked underestimation of the infection burden and overestimation of fatality rates6. Serological analysis of SARS-CoV-2-induced humoral immunity could reveal asymptomatic infections, but it is not yet widely applied7,8 and is complicated by the fact that coronavirus-induced antibody responses are variable and short-lived9,10. Coronavirus-induced cellular immunity is predicted to be more sustained, but remains poorly characterized. However, several T cell epitopes in the structural proteins of coronaviruses have been predicted or identified9,11,12,13. Notably, T helper (TH) cell responses and the generation of neutralizing antibodies may be interdependent9,14. Studies of the SARS-CoV epidemic in 2002–2003 have shown that adaptive immune responses directed against the spike glycoprotein (S) were protective9,15,16. Therefore, the induction of SARS-CoV-2-specific CD4+ T cells is likely to be critical in the instruction of affinity-maturated and potentially protective antibody responses17. We therefore examined the presence, frequencies and phenotypic characteristics of SARS-CoV-2 S-reactive T cells in patients with COVID-19 compared with SARS-CoV-2-unexposed healthy donors (HDs).
Identification of S-reactive CD4+ T cells
We identified S-reactive CD4+ T cells by flow cytometry according to their expression of CD40L and 4-1BB after in vitro stimulation with S peptides. To this end, we designed two peptide pools (15 amino acids with 11 amino acid overlaps) that spanned the entire S protein and that contained different amounts of putative MHC-II epitopes based on epitopes identified in SARS-CoV11,12,13 (Fig. 1a). SARS-CoV-2 S-peptide pool PepMix 1 (hereafter, S-I) spans the N-terminal part (amino acid residues 1–643) and includes 21 predicted SARS-CoV MHC-II epitopes (Fig. 1a, Extended Data Fig. 1 and Extended Data Table 1). The second peptide pool PepMix 2 (S-II) covered the C-terminal portion (amino acid residues 633–1273) and includes 13 predicted SARS-CoV MHC-II epitopes (Fig. 1a, Extended Data Fig. 1 and Extended Data Table 1). The peptides of the receptor-binding domain in subunit S1, which represents a major target of neutralizing antibodies, are included in S-I18,19.
For antigen-specific stimulation, peripheral blood mononuclear cells from patients and HDs were stimulated for 16 h with S-I and S-II peptide pools (for characteristics of patients and HDs, see Table 1 and Extended Data Tables 2, 3). Antigen-reactive CD4+ T cells were identified by co-expression of 4-1BB and CD40L, which enables the sensitive detection of S-reactive CD4+ T cells re-activated by T cell receptor engagement ex vivo20,21,22 (Fig. 2a, Extended Data Fig. 2 and Supplementary Information). In 12 (67%) and 15 (83%) out of 18 patients, we detected CD4+ T cells that reacted against the S-I and S-II peptide pools, respectively (Fig. 2b, d, e). Most patients with COVID-19 with critical disease showed no reactivity to the S-I peptide pool (Extended Data Fig. 3).
Notably, S-II-reactive CD4+ T cells—although at slightly lower frequencies compared with patients with COVID-19—could also be detected in 24 out of 68 HDs (35%), who are hereafter referred to as reactive healthy donors (RHDs) (Fig. 2c–e). S-I-reactive CD4+ T cells could be detected in only 6 out of the 24 RHDs, that is, in 5.8% of all HDs (Fig. 2d, e). All HDs were negative for IgG antibodies that were specific to the S1 subunit, in contrast to patients with COVID-19 (Fig. 2f). We further ruled out early SARS-CoV-2 infection at initial sampling by (1) direct standard diagnosis using PCR in 10 RHDs (data not shown); (2) serological testing (Fig. 2f); and (3) by repeated serological testing at least 28 days later for 65 out of 68 HDs (Extended Data Fig. 4).
We further phenotypically and functionally characterized S-reactive CD4+ T cells in additional patients with COVID-19 (Extended Data Table 4) and RHDs. Notably, in both groups, SARS-CoV-2 S-II-reactive CD4+ T cells exhibited a memory phenotype and a significant proportion of the cells expressed IFNγ, indicative of TH1 polarization (Fig. 2g and Extended Data Fig. 5a–d). Most S-reactive CD4+ T cells expressed IL-2 but only few cells expressed IL-17A (Extended Data Fig. 5a–d). Frequencies of S-II-reactive CD4+ T cells that expressed IFNγ were similar in patients and RHDs (Fig. 2g). Testing for TNF expression revealed that S-II-reactive IFNγ+CD4+ T cells from RHDs mostly co-expressed TNF, whereas S-II-reactive IFNγ+CD4+ T cells from patients with COVID-19 showed heterogenous TNF expression patterns (Extended Data Fig. 5e). This probably reflects the different disease stages of the acute SARS-CoV-2 infection of the individual patients included in our study. These results show that S-reactive CD4+ T cells with a predominantly TH1 memory phenotype are present not only in patients with COVID-19 but also in seronegative SARS-CoV-2-unexposed HDs.
S-reactive T cells in RHDs are cross-reactive to hCoVs
S-reactive CD4+ T cells from patients with COVID-19 equally targeted both the N-terminal (S-I) and C-terminal peptide pools (S-II) of S, whereas S-reactive CD4+ T cells from RHDs reacted significantly more strongly to the S-II peptide pool (Fig. 2d). S-II exhibits a higher homology to the human endemic coronaviruses (hCoVs; known as ‘common cold’ viruses) 229E, NL63, OC43 and HKU1 with regard to the SARS-CoV MHC-II epitopes, compared to the S-I peptide pool (Extended Data Table 1 and Extended Data Fig. 1). This suggests that S-reactivity in SARS-CoV-2-naive HDs originated from previous immune responses to hCoVs. We therefore tested 18 out of the 68 HDs for the presence of antibodies that are specific for the four endemic hCoVs. We detected IgG antibodies against all four hCoVs in all tested HDs, regardless of the presence of measurable S-reactive CD4+ T cells (Extended Data Fig. 6a). Frequencies of S-reactive or -cross-reactive CD4+ T cells in RHDs did not correlate with antibody levels against hCoVs, which potentially indicates that these antibodies have not been generated very recently. Similar findings have been obtained for other anti-viral CD4+ T cell responses, for example, after yellow fever vaccination (YFV-17D). CD4+ T cell responses showed a significant correlation with the later generation of high titres of neutralizing antibodies only at very early time points after YFV-17D vaccination23.
We next determined whether SARS-CoV-2 S-reactive CD4+ T cells in RHDs correlated with a CD4+ T cell response to the S protein of endemic hCoVs (ShCoV). To this end, peripheral blood mononuclear cells from HDs and RHDs were stimulated with S-I and S-II pools from SARS-CoV-2 and ShCoV-I and ShCoV-II pools of OC43 and 229E (Fig. 2h and Extended Data Fig. 6b–d). There was a strong positive correlation of CD4+ T cell reactivity against S-II and ShCoV-II of OC43 and 229E (r = 0.629 and r = 0.715, respectively) (Fig. 2h), whereas no or only a weak negative correlation was detected between S-I reactivity and reactivity towards ShCoV-I of OC43 and 229E (r = 0.037 and r = −0.259, respectively) (Extended Data Fig. 6b). No correlation was observed between reactivity to S-I or S-II and CMVpp65 (Extended Data Fig. 6c, d).
We next tested whether the S-reactive CD4+ T cells of RHDs responded to stimulation with ShCoV. To this end, S-II-reactive CD4+ T cells were isolated from three RHDs (RHD01, RHD07 and RHD15), expanded ex vivo for 12 days and subsequently restimulated with ShCoV-I and ShCoV-II of OC43 and 229E, with the S-II pool as positive control, or with S-I and a peptide pool from CMVpp65 as negative controls (Fig. 2i, j). Restimulation with the SARS-CoV-2 S-II peptide pool induced the highest frequencies of 4-1BB+CD40L+CD4+ T cells, whereas negligible responses were measured in the negative controls (S-I, CMVpp65 and unstimulated groups), demonstrating the high specificity of the established S-II-reactive CD4+ T cell lines (Fig. 2j). By contrast, strong responses were observed against the ShCoV-II peptide pools of the two hCoVs (Fig. 2j). These findings provide evidence of the cross-reactivity of SARS-CoV-2 S-II-reactive cells to ShCoV in the tested RHDs, suggesting that pre-existence of SARS-CoV-2-reactive T cells in seronegative SARS-CoV-2-naive individuals originates from previous immune responses to endemic hCoVs.
Activation signatures in patients with COVID-19
Finally, we assessed additional activation marker profiles on S-reactive T cells from patients with COVID-19 and RHDs. Expression of CD38, HLA-DR and Ki-67 has previously been shown to reliably characterize recently in vivo activated human T cells during acute and chronic infections24,25,26,27,28. Notably, S-reactive CD4+ T cells from patients largely expressed CD38, HLA-DR and Ki-67 (Fig. 3a–d). Most S-reactive T cells in patients co-expressed CD38 and HLA-DR (Fig. 3e), which is characteristic of effector T cell responses during acute viral infections24,26, whereas CD38 and Ki-67 co-expression was more variable (Fig. 3f). By contrast, S-reactive CD4+ T cells from RHDs did not express CD38, HLA-DR and Ki-67, or only at low frequencies (Fig. 3b–f), and co-expression was not observed (Fig. 3e, f). In patients, considerable proportions of the entire peripheral CD4+ and CD8+ T cell populations co-expressed CD38 and HLA-DR (data not shown); however, these cells could not be re-activated with our S peptide pools in vitro. These findings are consistent with results of a recent study that showed refractory T cell signatures in patients with COVID-1929. Additionally, a proportion of these CD38+HLA-DR+CD4+ T cells probably targets other structural proteins of SARS-CoV-2. We furthermore show that the presence of S-reactive CD4+ T cells and, in particular, of CD38-expressing cells among S-reactive CD4+ T cells was highly variable among patients during the course of COVID-19 disease (Fig. 3g, h).
Our study shows that S-reactive CD4+ T cells are present in patients with COVID-19 and in a considerable proportion of SARS-CoV-2-unexposed HDs. In light of the recent emergence of SARS-CoV-2, our data raise the possibility that such pre-existing S-reactive T cells represent cross-reactive clones that were probably acquired during previous infections with endemic hCoVs. hCoVs account for approximately 20% of ‘common cold’ upper respiratory tract infections and are ubiquitous, although they display winter seasonality30,31,32. On the basis of epidemiological data, it may be extrapolated that adults contract an hCoV infection, on average, every two to three years. Protective antibodies may wane mid-term but cellular immunity could remain10,13. Although the overall homology of the amino acid sequences of the S protein is relatively low compared with spike glycoproteins from hCoVs, there is an overlap in MHC-II epitopes especially in the C-terminal domain of the peptide pools used here (Fig. 1a and Extended Data Fig. 1). This may explain the preferential reactivity of CD4+ T cells to the C-terminal domain in one third of HDs.
The biological role of pre-existing S-cross-reactive CD4+ T cells in 35% of HDs remains unclear. However, assuming that these cells have a protective role in SARS-CoV-2 infection, they may contribute to our understanding of the divergent manifestations of COVID-19, and the notable resilience of children and young adults to symptomatic SARS-CoV-2 infection. Young adults and, especially, children in day-care centres have more frequent social contacts than elderly individuals, and this may therefore lead to a higher hCoV prevalence. This hypothesis requires further investigation in future longitudinal studies that assess the presence of pre-existing SARS-CoV-2-cross-reactive CD4+ T cells and their influence on the susceptibility to SARS-CoV-2 infection and age-related clinical outcomes of COVID-19.
SARS-CoV-neutralizing antibodies are associated with convalescence, and they have been detected 12 months after disease9. However, the durability of neutralizing antibody responses against SARS-CoV-2 remains unknown. Although antibodies against hCoV can wane within months after infection, hCoV reinfection is accompanied by low-level and short-lived virus shedding with only mild symptoms of short duration, which indicates humoral-independent residual immunity10. Cellular immunity has not yet been studied in this context. In mouse models, however, CD4+ as well as CD8+ T cell responses directed against structural proteins such as the spike or nucleocapsid proteins of SARS-CoV critically contributed to viral clearance15,33,34. Understanding the extent to which and how SARS-CoV-2-specific humoral or cellular immunity mediates durable protection against reinfection is of critical importance in the coming months.
Our study reveals pre-existing cellular SARS-CoV-2 cross-reactivity in a substantial proportion of SARS-CoV-2-seronegative HDs. This finding could have considerable epidemiological implications regarding herd immunity thresholds and projections for the COVID-19 pandemic. Our results provide a decisive rationale to initiate worldwide prospective studies to assess the contribution of pre-existing, potentially region-dependent, SARS-CoV-2-cross-reactive immunity to the diverse clinical outcomes of SARS-CoV-2 infection. Together with currently introduced serological tests, the data generated by such studies may critically inform evidence-based risk evaluation, patient monitoring, adaptation of containment methods and vaccine development.
No statistical methods were used to predetermine sample size. The experiments were not randomized and the investigators were not blinded to allocation during experiments and outcome assessment.
The study was approved by the Institutional Review Board of the Charité (EA2/066/20). After providing written informed consent, 68 HDs (Table 1 and Extended Data Table 3) and 18 and 7 additional patients with COVID-19 (Table 1 and Extended Data Table 2, 4) were included in the study. Patients with COVID-19 who tested positive for SARS-CoV-2 RNA in nasopharyngeal swabs were recruited at Charité Campus Virchow-Klinikum, Berlin, between 1 March and 2 April 2020. All patients with COVID-19 were enrolled in the Berlin prospective observation COVID-19 study (PA-COVID-19)35. Disease severity was grouped on the basis of the requirement for supplementary oxygen or ventilation (mild, hospitalized, no supplementary oxygen; severe, hospitalized, supplementary oxygen (including high-flow oxygen); critical, hospitalized, invasive ventilation). For intracellular cytokine and memory T cell staining, seven additional patients with COVID-19 (Extended Data Table 4) were enrolled at later time points and five RHDs were re-recruited. To retrospectively validate SARS-CoV-2 seronegativity, all HDs were re-invited between 4 and 7 May 2020 for re-assessment of anti-S1 IgG titres. In total, 65 out of 68 HDs could be re-recruited and all HDs were seronegative for SARS-CoV-2 (Extended Data Fig. 4).
Anti-SARS-CoV-2 IgG ELISA was performed using a commercial kit (EUROIMMUN) as described and validated previously8. Recombinant immunofluorescence assays to determine IgG titres against hCoV were performed using VeroB4 cells that expressed cloned recombinant spike proteins from hCoV-229E, hCoV-NL63, hCoV-OC43 and hCoV-HKU1, as previously described36.
Cell isolation and stimulation
Peripheral blood mononuclear cells were isolated from heparinized whole blood by density gradient centrifugation according to manufacturer’s instructions (Leucosep tubes, Greiner; Biocoll, Bio&SELL). Stimulation was performed with 5 × 106 peripheral blood mononuclear cells in RPMI 1640 medium (Gibco) supplemented with 10% heat-inactivated AB serum (Pan Biotech), 100 U/ml penicillin (Biochrom), 0.1 mg/ml streptomycin (Biochrom) and PepMix SARS-CoV-2 spike glycoprotein (JPT) peptide pool 1 or 2 in the presence of 1 μg/ml purified anti-CD28 antibody (clone CD28.2, BD Biosciences). The PepMix SARS-CoV-2 spike glycoprotein pool 1 covering the N-terminal amino acid residues 1–643 (abbreviated to ‘S-I’ (N-term)) contained 158 15-mers that overlapped by 11 amino acids. PepMix SARS-CoV-2 spike glycoprotein pool 2 covered the C-terminal amino acid residues 633–1273 (abbreviated to ‘S-II’ (C-term)) contained 156 15-mers that overlapped by 11 amino acids and one 17-mer at the C terminus, that is, 157 peptides in total. Both peptide pools were used at 1 μg/ml per peptide. Further details on the peptide pools and predicted MHC-II epitopes are provided in Fig. 1, Extended Data Fig. 1 and Extended Data Table 1. Stimulation controls were performed with equal concentrations of DMSO in PBS (unstimulated) or 1.5 mg SEB/1.0 mg TSST1 (Sigma-Aldrich) and PepMix HCMVA (pp65) (>90%; CMVpp65) (JPT) in the presence of 1 μg/ml purified anti-CD28 antibody (clone CD28.2, BD Biosciences) as positive controls. Incubation was performed at 37 °C, 5% CO2 for 16 h with 10 μg/ml brefeldin A (Sigma-Aldrich) added after 2 h. Stimulation was stopped by incubation in 2 mM EDTA for 5 min. Stimulation with hCoV spike glycoprotein (ShCoV) peptide pools was performed using the conditions described above but with 1 μg/ml per peptide of the following peptide pools: PepMix hCoV-229E spike glycoprotein pool 1 or 2 or PepMix hCoV-OC43 spike glycoprotein pool 1 or 2 (all JPT).
After stimulation, staining of surface antigens was carried out for 15 min with the following fluorochrome-conjugated antibodies titrated to their optimal concentrations: CD38-PE-Vio770 (clone REA671, Miltenyi, 1:400), CD69-APC-Cy7 (FN50, BioLegend, 1:100), HLAD-DR-VioGreen (REA805, Miltenyi, 1:50), CD4-BrilliantViolet605 (RPA-T4, BioLegend, 1:200), CD8-PerCP (SK1, BioLegend, 1:100) with 1 mg/ml beriglobin (CSL Behring) added before the staining. To exclude dead cells, Zombie Yellow fixable viability staining (BioLegend) was added for the last 10 min of incubation. Fixation and permeabilization were performed with eBioscience FoxP3 fixation and PermBuffer (Invitrogen) according to the manufacturer’s protocol and intracellular staining was carried out for 30 min in the dark at room temperature with beriglobin added before staining with 4-1BB-PE (4-1BB is also known as CD137; clone 4B4-1, BD, 1:10), CD40L-APC (CD40L is also known as CD154; 5C8, Miltenyi, 1:40), IFNγ-AlexaFluor700 (B27, BD, 1:50), TNF-PacificBlue (MAb11, BioLegend, 1:100) and Ki-67-AlexaFluor488 (B56, BD, 1:100). To assess naive/memory T cell phenotypes and cytokine expression, the following antibodies were used: surface staining was performed with CD3-V500 (SP34-2, BD, 1:50), CD8-PerCP (SK1, BioLegend, 1:100), CD4-BrilliantViolet605 (RPA-T4, BioLegend, 1:200), CCR7-AlexaFluor488 (G043H7, BioLegend, 1:150), CD45RA-PE-Cy7 (HI100, BioLegend, 1:200). IFNγ-AlexaFluor700 (B27, BD, 1:100), CD40L-BrilliantViolet421 (24-31, BioLegend, 1:200), IL-2-APC (5344.111, BD, 1:200), 4-1BB-PE (4B4-1, BD, 1:10) and IL-17A-APC-Cy7 (BL168, BioLegend, 1:20) were used for intracellular staining after fixation and permeabilization using BD FACSLysing Buffer and BD Perm2 Buffer, according to the manufacturer’s instructions. Samples were measured on a MACSQuant Analyzer 16 using MACSQuantify software (v.2.13). Instrument performance was monitored daily with Rainbow Calibration Particles (BD).
Cell enrichment, expansion and restimulation
S-II-reactive T cells were enriched by magnetic cell sorting (MACS) from peripheral blood mononuclear cells stimulated with PepMix SARS-CoV-2 spike glycoprotein peptide pool 2 (JPT) in the presence of 1 μg/ml purified anti-CD28 (clone CD28.2, BD Biosciences) and 1 μg/ml anti-CD40 (clone 5C3, BioLegend) antibodies. After stimulation for 16 h, cells were stained with CD40L-APC and 4-1BB-PE and first enriched with anti-APC MultiSort MicroBeads (Miltenyi) according to the manufacturer’s instructions. After the release of anti-APC-MicroBeads, a second enrichment was performed with anti-PE MicroBeads (Miltenyi). Purity was checked each time to >80% of alive cells. Antigen presenting feeder cells were generated by CD3 MicroBead (Miltenyi) depletion of the CD40L-APC-negative fraction and subsequent inactivation by irradiation at 50 Gy. The irradiated feeder cells were co-cultured with the enriched 4-1BB+CD40L+ T cells at a ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 10% heat-inactivated AB serum (Pan Biotech), 100 U/ml penicillin (Biochrom), 0.1 mg/ml streptomycin (Biochrom) in the presence of 10 ng/ml IL-7 and IL-15 (both Miltenyi) for 12 days followed by 2-day cytokine starvation before restimulation. Restimulation was carried with the conditions described above and additionally with 1 μg/ml per peptide of the following peptide pools: PepMix hCoV-229E spike glycoprotein pool 1 or 2 or PepMix hCoV-OC43 spike glycoprotein pool 1 or 2 (all JPT).
Data analysis and statistics
Sequence alignments were performed using R (v.3.6.1) including package ClustalX37 and using the Needlemann–Wunsch algorithm38. Flow cytometry data were analysed with FlowJo v.9.9.6 (FlowJo). Microsoft Excel (v.14.1.0) and Prism 5 and 8 (GraphPad) were used for plotting and statistical analysis. In stimulation experiments, frequencies of activated CD4+ T cells were background-subtracted, with the frequency in the unstimulated control sample representing the background. Non-parametric testing was used to compare cell frequencies and antibody titres between groups (two-tailed Mann–Whitney U-test). n indicates the number of donors.
Further information on research design is available in the Nature Research Reporting Summary linked to this paper.
All flow cytometry data are made available at www.FlowRepository.org (experiment ID: FR-FCM-Z2K3). The individual gating strategies for all donors are shown in Supplementary Information.
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We thank U. Klein and H.-P. Herzel for discussion; T. Kaiser and J. Kirsch from the Flow Cytometry Core Facility (FCCF) of the DRFZ for technical help; and B. Timmerman from the Sequencing Core Facility of the Max Planck Institute for Molecular Genetics for discussion. This work was supported by the German Research Foundation (KFO339 to J.B. and F.F., SFB-TR84 projects A4 and B6 to S.H., B8 to M.M., C6 to M.W., C8 and C10 to L.E.S., and C9 to M.W. and N.S.) and by the German Federal Ministry of Education and Research (BMBF-RAPID to S.H. and C.D., and CAPSyS to M.W. and N.S.). This work was additionally funded by the Federal Ministery of Health through a resolution of the German Bundestag to A.T., J.B., L.H. and M.D.
F. Kern, U.R. and H.W. are employed at JPT Peptide Technologies, who have provided peptide pools for this work. F. Kern also part-owns and is inventor on a patent describing the use of overlapping peptide pools for the stimulation of T cells. Until this patent expires, he will receive royalties on JPT PepMix sales. J.S. and S.M. are employed at Miltenyi Biotec, who provided reagents and devices for this study. All other authors declare no competing interests.
Peer review information Nature thanks Akiko Iwasaki and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Extended data figures and tables
Extended Data Fig. 1 Homology of reported MHC-II epitopes in the spike glycoprotein of SARS-CoV compared with SARS-CoV-2 and endemic hCoV strains.
For each epitope, the respective section from a global sequence alignment between SARS-CoV, SARS-CoV-2 and the hCoVs NL63, 229E, HKU1 and OC43 is shown. Identical residues are colour-coded from white (no identity) to red (100% identity). Reported MHC-II epitopes are described further in Extended Data Table 1.
Extended Data Fig. 2 Exemplary analyses gates and dot plots from patients with COVID-19, RHDs and HDs.
FACS analysis was performed to determine the frequencies of S-I-reactive and S-II-reactive CD4+ T cells and the ratios of CD38+, HLA-DR+ and Ki-67+ cells among the S-I-reactive and S-II-reactive CD4+ T cells.
Extended Data Fig. 3 Most S-I-non-reactive and S-II-non-reactive patients with COVID-19 had a critical disease stage.
Frequencies of S-I- and S-II-reactive CD4+ T cells in patients with COVID-19 are grouped according to disease severity for patients with mild (n = 7), severe (n = 5) or critical (n = 6) disease.
Extended Data Fig. 4 Repeated serology of HDs confirms unexposed status of HDs and RHDs.
SARS-CoV-2 S1 serology of HDs (n = 43) and RHDs (n = 22) more than 28 days after initial sampling. Anti-S1 IgG titres are expressed as a ratio normalized to the calibration well, which contained the provided control serum (as described in the manufacturing instructions).
Extended Data Fig. 5 Expression of cytokines and differentiation markers in S-I-reactive and S-II-reactive CD40L+4-1BB+CD4+ T cells from patients with COVID-19 and RHDs.
a, Gating schematic of one representative donor to select for CD3+CD4+ T cells and exclude dead cells and doublets.b, c, Determination of the differentiation marker and cytokine profiles of S-I- and S-II-reactive CD4+ T cells shown for one patient with COVID-19 and one RHD after S-I and S-II peptide pool stimulation, respectively. SARS-CoV-2 S-reactive CD4+ T cells were defined by CD40L and 4-1BB expression after stimulation and are displayed as red dots. Numbers are the frequencies of cytokine-expressing S-I/S-II-reactive CD4+ T cells and the distribution of the naive (CCR7+CD45RA+) and memory (CCR7+CD45RA− or CCR7−CD45RA−) phenotypes of S-I/S-II-reactive CD4+ T cells, respectively. d, Diagrams summarizing the cytokine and differentiation marker distribution frequencies of S-I- and S-II-reactive CD4+ T cells from patients with COVID-19 (n = 7) and RHDs (n = 5). e, Expression of TNF and IFNγ in S-II-reactive CD4+ T cells from patients and RHDs. Five representative plots of TNF versus IFNγ expression in CD40L+4-1BB+CD4+ T cells from RHDs and patients with COVID-19; gating strategy as shown in Fig. 2.
Extended Data Fig. 6 hCoV-specific IgG antibody titres in HDs and RHDs and specificity of SARS-CoV-2-reactive T cells in HDs.
a, IgG antibody titres against endemic coronavirus strains (hCoVs). VeroB4 cells expressing recombinant spike proteins of hCoV-HKU1, hCoV-OC43, hCoV-229E and hCoV-NL63 were used in a recombinant immunofluorescence assay (rIFA) as described previously36. Titres above 1:20 dilution were considered positive (indicated by the dashed line). HD, n = 9; RHD, n = 9. b–d, Frequencies of SARS-CoV-2 S-I-reactive CD4+ T cells in HDs do not correlate with frequencies of ShCoV-I-reactive or CMV-reactive CD4+ T cells. Frequencies of SARS-CoV-2 S-II-reactive CD4+ T cells in HDs do not correlate with frequencies of CMV-reactive CD4+ T cells. b, Scatter plot of ShCoV-I-reactive CD4+ T cell frequencies (229E, n = 12; OC43, n = 9) and SARS-CoV-2 S-I-reactive CD4+ T cell frequencies. c, Scatter plot of SARS-CoV-2 S-I-reactive CD4+ T cell and CMV-reactive CD4+ T cell frequencies (n = 21). d, Scatter plot of SARS-CoV-2 S-II-reactive CD4+ T cell and CMV-reactive CD4+ T cell frequencies (n = 21). b–d, Correlation coefficients (r) were calculated by Pearson correlation and the related P values are based on t-distributions.
The Supplementary File displays the individual gating strategy for all donors.
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Braun, J., Loyal, L., Frentsch, M. et al. SARS-CoV-2-reactive T cells in healthy donors and patients with COVID-19. Nature 587, 270–274 (2020). https://doi.org/10.1038/s41586-020-2598-9
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