INDUCTION OF HUMAN T-CELLS THAT COEXPRESS CD4 AND CD8 BY AN IMMUNOMODULATORY PROTEIN PRODUCED BY ACTINOBACILLUS-ACTINOMYCETEMCOMITANS

Citation
Bj. Shenker et al., INDUCTION OF HUMAN T-CELLS THAT COEXPRESS CD4 AND CD8 BY AN IMMUNOMODULATORY PROTEIN PRODUCED BY ACTINOBACILLUS-ACTINOMYCETEMCOMITANS, Cellular immunology, 164(1), 1995, pp. 36-46
Citations number
29
Categorie Soggetti
Cell Biology",Immunology
Journal title
ISSN journal
00088749
Volume
164
Issue
1
Year of publication
1995
Pages
36 - 46
Database
ISI
SICI code
0008-8749(1995)164:1<36:IOHTTC>2.0.ZU;2-5
Abstract
Actinobacillus actinomycetemcomitans, a gram-negative, capnophilic bac terium, is associated with several human diseases and is the suspected etiologic agent in certain forms of periodontal disease. We have prev iously shown that this organism produces an immunosuppressive factor ( ISF) which is capable of inhibiting both T- and B-cell activation. Fur thermore, these effects appear to be associated with the activation of a population of suppressor cells. We now report that the ISF induces a unique population of CD4(+)CD8(+) dual-positive T-cells. By utilizin g multiparameter how cytometric analysis, we were able to detect the p resence of dual-positive cells in cultures of human T-cells treated wi th PHA and ISF. The cells appeared within 48 hr and their induction wa s dependent upon the presence of both CD4 and CD8 cells in the culture . Dual expression of CD4 and CD8 was stable in that the cells continue d to express both surface proteins after being sorted and cultured for an additional 24 hr. Phenotypic analysis indicates that these cells a re also CD3(+), CD2(+), CD5(+), TCR alpha beta(+), CD45RA(+) (and RO()), and CD29(+). The dual-positive cells express surface markers assoc iated with T-cell activation: CD25(+), CD69(+), CD71(+), and HLA-DR(+) . In contrast, the cells were negative for CD34, CD57, CD56, and CD16. Cell cycle analysis indicates that >80% of the dual-positive cells we re in the S phase. Finally, functional analysis of these cells indicat es that they are capable of suppressing the proliferative response of autologous T-cells to PHA. (C) 1995 Academic Press, Inc.