TY - JOUR
T1 - Interactions between autologous T cell clones
AU - Naor, David
AU - Essery, Gail
AU - Tarcic, Nora
AU - Kahan, Melvyn
AU - Feldmann, Marc
PY - 1990/7
Y1 - 1990/7
N2 - A human CD4 clone (Mx9/9) using the Vβ8 receptor was used as antigen to generate autologous clones (termed anti-Mx9/9 clones) which proliferate in response to this clone, but not other autologous clones. This was used as an experimental model to explore the specific interactions between autologous T cells. Anti-HLA-DR monoclonal antibodies inhibited the response of the anti-Mx9/9 clones, suggesting that these clones recognize their target antigen in association with HLA-DR. Because of the specificity of the anti-Mx9/9 clones for the initiating clone (Mx9/9), but not any other autologous Vβ8- or Vβ8+ CD4 clones, the target antigen seems to be part of the T cell receptor, but not Vβ8 itself. However, the anti-Mx9/9 clones responded also to the autologous EBV line, and thus the target antigen is not known. The regulatory activity of the anti-Mx9/9 clones was assayed by coculture with their target clone. A variety of responses were seen, both inhibitory and stimulatory, which varied depending on the "conditions" of the T cells used. These results suggest that T cells interact in a complex network, perhaps as complex as the regulatory interactions between antibody molecules and B cells.
AB - A human CD4 clone (Mx9/9) using the Vβ8 receptor was used as antigen to generate autologous clones (termed anti-Mx9/9 clones) which proliferate in response to this clone, but not other autologous clones. This was used as an experimental model to explore the specific interactions between autologous T cells. Anti-HLA-DR monoclonal antibodies inhibited the response of the anti-Mx9/9 clones, suggesting that these clones recognize their target antigen in association with HLA-DR. Because of the specificity of the anti-Mx9/9 clones for the initiating clone (Mx9/9), but not any other autologous Vβ8- or Vβ8+ CD4 clones, the target antigen seems to be part of the T cell receptor, but not Vβ8 itself. However, the anti-Mx9/9 clones responded also to the autologous EBV line, and thus the target antigen is not known. The regulatory activity of the anti-Mx9/9 clones was assayed by coculture with their target clone. A variety of responses were seen, both inhibitory and stimulatory, which varied depending on the "conditions" of the T cells used. These results suggest that T cells interact in a complex network, perhaps as complex as the regulatory interactions between antibody molecules and B cells.
UR - http://www.scopus.com/inward/record.url?scp=0025297503&partnerID=8YFLogxK
U2 - 10.1016/0008-8749(90)90043-Q
DO - 10.1016/0008-8749(90)90043-Q
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C2 - 1972658
AN - SCOPUS:0025297503
SN - 0008-8749
VL - 128
SP - 490
EP - 502
JO - Cellular Immunology
JF - Cellular Immunology
IS - 2
ER -