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. 2004 Jul 11;10(8):871–875. doi: 10.1038/nm1080

Table 1.

Repertoire analysis of IgG memory B cells

Months after infection Positive cultures/total cultures screened (%)a
ELISA Spike-staining
2 275/480 (57.3%) ND
4 123/480 (25.6%) 12/576 (2.1%)
6 44/480 (9.2%) 21/768 (2.7%)
8 20/480 (4.1%) 94/3,102 (3%)

aFraction of cultures screening positive in the SARS-CoV ELISA or staining SARS-CoV spike transfectants at different time points after infection. IgG+ memory B cells were cultured at 10 cells per well in the presence of EBV and CpG 2006. Culture supernatants were analyzed after 2 weeks. There was no overlap between cultures screening positive by either assay, indicating that the assays detect distinct antibody specificities. SARS-CoV was not detectable in culture supernatant or in EBV-B cells, as determined by cytopathic assay on Vero cells and by RT-PCR (data not shown). ND, not determined because the assay was not available at the time of the analysis.