Figure 3.
Figure 3. Vaccine-specific IgG are produced by both the CD19+and the CD19−ASC subsets. (A) BD CD19+ and CD19− ASC antigen-specific ELISpot results for Daptacel and Fluzone (unpaired Student t test, P < .0327, CD19+ mean ± SEM 5.810 ± 1.498, n = 10, CD19− mean ± SEM 15.29 ± 3.814, n = 10). (B) Representative ELISpot wells from 3000 CD19+ and CD19− FACS sorted ASCs from BM. (C) 3000 CD19+ and CD19− ASCs from spleen were sorted onto Daptacel (n = 4), Fluzone (n = 5), MMR (n = 2), Varicella (n = 2), or IPOL (n = 3) vaccine antigen precoated ELISpot plates and detected for total IgG. (D) Representative ELISpot wells showing sorted ASCs from either CD19+ or negative spleen subsets. (E) 10 000 (Flu/Dap) and 30 000 (polio) CD19+ ASCs or B cells were FACS sorted from BM, spleen, and tonsil, which indicated antigen-specific CD19+ ASCs existed in all tissues. Ag., antigen; Dap., Daptacel; Flu., Fluzone; MMR, measles, mumps, and rubella; Var., Varicella.

Vaccine-specific IgG are produced by both the CD19+and the CD19ASC subsets. (A) BD CD19+ and CD19 ASC antigen-specific ELISpot results for Daptacel and Fluzone (unpaired Student t test, P < .0327, CD19+ mean ± SEM 5.810 ± 1.498, n = 10, CD19 mean ± SEM 15.29 ± 3.814, n = 10). (B) Representative ELISpot wells from 3000 CD19+ and CD19 FACS sorted ASCs from BM. (C) 3000 CD19+ and CD19 ASCs from spleen were sorted onto Daptacel (n = 4), Fluzone (n = 5), MMR (n = 2), Varicella (n = 2), or IPOL (n = 3) vaccine antigen precoated ELISpot plates and detected for total IgG. (D) Representative ELISpot wells showing sorted ASCs from either CD19+ or negative spleen subsets. (E) 10 000 (Flu/Dap) and 30 000 (polio) CD19+ ASCs or B cells were FACS sorted from BM, spleen, and tonsil, which indicated antigen-specific CD19+ ASCs existed in all tissues. Ag., antigen; Dap., Daptacel; Flu., Fluzone; MMR, measles, mumps, and rubella; Var., Varicella.

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