This study was performed to investigate T-cell traffic to periodontal
tissues during infection with a periodontal pathogen Actinobacillus ac
tinomycetemcomitans (Aa). Rowett rat T-cell clones, A3 (CD4(+) CD8(-),
alpha beta TCR+, NKRP-1(-), specific to Aa) and G2 (CD4(-) CD8(-), al
pha beta TCR+, NKRP-1(+), which reacts to Aa, Gram-negative and -posit
ive bacteria), both expressed the same prominent adhesion molecules (L
FA-1, VLA-4) to the same extent. Binding of bath T-cell clones to rat
endothelial cells in vitro was blocked by antibody to VLA-4. Rowett ra
ts were infected with Aa and infused with Aa-stimulated, isogenic T-cl
one lymphocytes that had been labelled in vitro with (125)IUdR. Radioa
ctivity associated with recovery of clone A3, but not G2, was signific
antly elevated in the gingivae of infected rats, suggesting migration
to infected animals' gingival tissues. Migration of radioactive Aa-spe
cific A3 clone cells traced by autoradiography reached a maximum at 24
hr (1.2% of total lymphocytes as radiolabelled cells in infected ging
iva versus 0.6% in non-infected), indicating an apparent antigen-direc
ted retention in infected rats' gingival tissues. The G2 clone was not
retained in the gingival tissues (0.20% of total lymphocytes as radio
labelled cells in infected gingiva versus 0.26% in non-infected). Howe
ver, the possibility of A3 retention directed by inflammation or tissu
e-selective homing could not be excluded. In further experiments, othe
r adoptively transferred T-clone lymphocytes [clones G23 (Th1) and F13
(Th2)] with specificity for the 29 000 MW outer membrane protein of A
a with the same prominent adhesion molecules could be recovered from r
at gingivae previously challenged with this antigen. However, transfer
red T-clone lymphocytes [clone G26 (Th1)] with specificity for a diffe
rent Aa antigen were not recovered. Therefore, the dynamics of cell en
try into periodontal lesions vary for activated T lymphocytes with dif
ferent antigenic specificities, indicating the significance of antigen
in lymphocyte traffic to periodontal tissues.