Lymphoid environment limits superantigen and antigen-induced T cell proliferation at high precursor frequency.


Autoria(s): Attinger A.; MacDonald H.R.; Acha-Orbea H.
Data(s)

2001

Resumo

After superantigen challenge a significant proportion of superantigen-reactive T cells remain undivided. We provide evidence that the lymphoid environment limits T cell proliferation in the secondary lymphoid organs when the frequency of superantigen reactive T cells is unusually high. We monitored T cell proliferation and the percentage of undivided cells when the frequency of superantigen-reactive T cells was low (1%), intermediate (15%) or high (30-100%) by transferring fluorescently labeled cells into different recipients. When the frequency was low, practically all the reactive T cells entered cell cycle and proliferated maximally. At intermediate frequencies a large proportion of reactive T cells did not enter cell cycle and the whole population divided less. A further increase in reactive T cells did not alter the percentage of undivided cells but induced a further decrease in the number of cell divisions. Interestingly, the observations made with superantigens were confirmed with peptide antigen and TCR-transgenic mice. Moreover, in vivo and in vitro data suggest that dendritic cells are the most likely candidates in limiting T cell proliferation in the lymphoid environment. In conclusion, we show that the availability of APC in the lymphoid environment can quantitatively limit T cell priming.

Identificador

http://serval.unil.ch/?id=serval:BIB_39D88E86D7CF

isbn:0014-2980 (Print)

pmid:11241294

doi:10.1002/1521-4141(200103)31:3<884::AID-IMMU884>3.0.CO;2-M

isiid:000167611900025

Idioma(s)

en

Fonte

European Journal of Immunology, vol. 31, no. 3, pp. 884-893

Palavras-Chave #Adoptive Transfer; Animals; Antigen-Presenting Cells/immunology; Antigens/immunology; Cells, Cultured; Enterotoxins/immunology; Fluoresceins/chemistry; Fluorescent Dyes/chemistry; Lymphocyte Activation; Lymphoid Tissue/immunology; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Transgenic; Receptors, Antigen, T-Cell, alpha-beta/genetics; Receptors, Antigen, T-Cell, alpha-beta/physiology; Stem Cells/immunology; Succinimides/chemistry; Superantigens/immunology; T-Lymphocytes/immunology; T-Lymphocytes/transplantation
Tipo

info:eu-repo/semantics/article

article