Interactions between autologous T cell clones

David Naor*, Gail Essery, Nora Tarcic, Melvyn Kahan, Marc Feldmann

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)490-502
Number of pages13
JournalCellular Immunology
Volume128
Issue number2
DOIs
StatePublished - Jul 1990
Externally publishedYes

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