TABLE 2.
Cell type | Fragmentb | RVS IgAa (OD units) | RVS IgAb (OD units) | Total IgAa (ng/ml) | Total IgAb (ng/ml) |
---|---|---|---|---|---|
B1a/non-B1b | SI | 0 | 1.68 ± 0.54 | 160 ± 32 | 306 ± 93 |
LI | 0 | 1.31 ± 0.60 | 212 ± 58 | 374 ± 136 | |
B1b/non-B1a | SI | 2.07 ± 0.23 | 0 | 285 ± 70 | 122 ± 13 |
LI | 2.05 ± 0.50 | 0 | 367 ± 114 | 201 ± 63 | |
PECa | SI | 3.25 ± 0.60 | 0 | 204 ± 63 | 0 |
LI | 3.22 ± 0.43 | 0 | 228 ± 62 | 0 | |
PECb | SI | 0 | 1.82 ± 0.04 | 0 | 156 ± 1 |
LI | 0 | 1.78 ± 0.28 | 0 | 165 ± 6 |
The production of RV-specific and total IgA in small and large intestinal lymphoid tissues of RV-infected SCID mice reconstituted with peritoneal B1 and non-B1 cells of a versus b allotypes is shown. SCID mice were inoculated with EDIM RV at 12 weeks of age and 3 weeks later were reconstituted with reciprocal combinations of peritoneal B1 and non-B1 cells of allotypes a versus b (indicated as roman superscripts). Unseparated peritoneal exudate cells (PEC) of each allotype served as positive controls. Cultures of small and large intestine fragments were performed 2 to 3 months later, and supernatants were tested by ELISA for the presence of RV-specific and total IgA of allotypes a and b. The data represent the means ± the SEM. The number of fragments per tissue per group of mice ranged from 12 to 24.
SI, small intestine; LI, large intestine.