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. 2012 Apr;19(4):477–489. doi: 10.1128/CVI.05642-11

Table 2.

Summary of antigens that induced significant T cell proliferation in three experiments using 2-week cell lines from S. aureus-immunized calves

Expt no. Proliferative response of T cell lines to the indicated antigen(s) by animala
30864 (12/16)b
30900 (23/27)
30904 (11/16)
30916 (3/24)
30919 (10/22)
Antigen SI Antigen SI Antigen SI Antigen SI Antigen SI
1 NWMN_0364 25.7c NWMN_2086 9.6c NWNM_0601 38.2c NWMN_0601 2.3c NWMN_2086 8.3c
NWMN_0601 24.4c NWMN_0364 2.4 NWMN_1999 4.3
2 NWMN_0364 46.7c NWMN_2086 17.2c NWMN_0601 6.7c NWMN_0601 5.3c NWMN_2086 9.3c
NWMN_0601 20.1c NWMN_0601 3.0d NWMN_0429 4.4 NWMN_2086 2.2d NWMN_2469 2.6d
NWMN_0161 25.3 NWMN_2270 2.3d
NWMN_0390 10.4 NWMN_2318 7.8d
NWMN_2319 7.2d
NWMN_2320 2.2d
NWMN_2469 9.6d
3 NWMN_0364 38.9c NWNM_2086 4.2c NWMN_0601 2.7c NWMN_0601 18.9c NWMN_2086 6.0c
NWMN_0601 19.3c NWMN_0601 2.4d NWMN_1733 2.7 NWMN_2086 12.5d NWMN_2469 13.7d
NWMN_2086 9.4 NWNM_2320 4.7 NWMN_2270 12.8d NWMN_2320 5.3
NWMN_2318 29.3d
NWMN_2319 24.0d
NWMN_2320 16.2d
NWMN_2469 34.5d
a

Different batches of IVTT-expressed proteins were tested in each experiment. Antigens were determined to induce significant responses based on the following criteria: mean cpm of >1,000, SI of >2.0, and P of <0.05 compared to medium, beads, and VirB9 beads. Significant proliferation was determined using ANOVA with Dunnett's posttest for multiple comparisons (P < 0.05). Assays were performed using 43 antigens tested in triplicate from three expression experiments. SI was determined as the mean cpm in response to 1 or 5 μg/ml S. aureus antigen/mean cpm in response to Virb9 beads, whichever was higher.

b

MHC class II haplotypes were determined by RFLP analysis of exon II from the DRB3 locus. For example, 12/16 refers to the RFLP haplotypes designated DRB3 12 and DRB3 16, each inherited from one parent.

c

Antigens that induced significant proliferation in three independent assays for each animal.

d

Antigens that induced significant proliferation in two independent assays for each animal.