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Extra resources for Annual Review of Immunology Volume 22 2004

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These studies demonstrate that the collaborative recognition of distinct microbial components by different classes of innate immune receptors (CLRs and TLRs) is crucial for orchestrating inflammatory or inhibitory responses. The balance between TLR stimulation and C-type lectin occupation may fine-tune regulatory mechanisms to allow appropriate immune responses. The inflammatory and pathogenic consequence of this recognition is dependent on both the receptor repertoire and the functional cooperation between the signals generated downstream of receptor-ligand interaction.

Evolutionary conservation of surface molecules that distinguish T lymphocyte helper/inducer and cytotoxic/suppressor subpopulations in mouse and man. J. Exp. Med. 153:310–23 Roederer M, Dubs JG, Anderson MT, Raju PA, Herzenberg LA. 1995. CD8 naive T cell counts decrease progressively in HIVinfected adults. J. Clin. Invest. 95:2061– 66 Watanabe N, De Rosa SC, Cmelak A, Hoppe R, Herzenberg LA, Roederer M. 1997. Long-term depletion of naive T cells in patients treated for Hodgkin’s disease. Blood 90:3662–72 Sahaf B, Heydari K, Herzenberg LA.

22:33-54. org by HINARI on 09/01/07. For personal use only. ANTIGEN RECOGNITION BY C-TYPE LECTINS ON DC 43 At high concentrations, HIV-1 can infect DCs in cultures that coexpress CD4 and chemokine receptors (57, 101, 102). HIV-1 can replicate in immature as well as in mature DCs that interact with T cells (82, 103). In particular, the initial quantity of virus that enters the mucosal tissues may be decisive in whether DCs become infected by HIV-1 or whether the virus is captured for efficient transinfection of T cells (80).

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