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2000
Volume 5, Issue 4
  • ISSN: 1570-162X
  • E-ISSN: 1873-4251

Abstract

The antimicrobial peptide LL-37 is the only cathelicidin that has been described in humans. LL-37 exerts chemotactic, immunomodulatory and angiogenic effects; activities that are mediated through binding to the formyl peptide receptor like (FPRL)-1 receptor. Agonistic ligation of FPRL-1 can also induce down-regulation of HIV-1 chemokine receptors and reduce susceptibility to HIV-1 infection in vitro. Therefore, we have evaluated the capacity of LL-37 to inhibit HIV-1 infection in vitro. Here we demonstrate that LL-37 inhibits HIV-1 replication in PBMC, including primary CD4+ T cells. This inhibition was readily reproduced using various HIV-1 isolates without detectable changes in the target cell expression of HIV-1 chemokine receptors. Accordingly, the HIV-1 inhibitory effect was shown to be independent of FPRL-1 signalling. Given the epithelial expression of LL-37, it may contribute to the local protection against HIV-1 infection.

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/content/journals/chr/10.2174/157016207781023947
2007-07-01
2025-09-02
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/content/journals/chr/10.2174/157016207781023947
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  • Article Type:
    Research Article
Keyword(s): Antimicrobial peptide; cathelicidin; FPRL-1; HIV-1; innate immunity; LL-37
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