Haemaphysalis longicornis (Hl) as members of the ixodid tick inhabits lots of grass thicket of field and mountain. Ticks are blood-feeding ectoparasites that can mediate a variety of diseases to human and animals, causing Lyme disease, Rocky Mountain spotted fever, and human monocytic ehrlichiosis. Particularly, ticks can trigger an inflammatory response representing symptoms about swelling and itching in human. The aim of this study is to investigate the effect of H. longicornis extract (HlE) on production of inflammatory cytokines and their mRNA in human monocytic THP-1 cells. In a time- and dose-dependent manner, human monocytic THP-1 cells was treated with HlE. Supernatants were analyzed for the production of cytokines using enzyme-linked immunosorbent assay (ELISA). mRNA level in the culture cells was measured by a reverse transcriptase-polymerase chain reaction (RT-PCR). As a result of this study, HlE significantly induced secretion of IL-6, IL-8, and MCP-1 in THP-1 cells. These results suggest that HlE increase the release of proteins and mRNAs level of inflammatory cytokines in THP-1 cells. HlE may play a role in contributing to inflammatory diseases through stimulation of immune cells. Further research of H. longicornis is needed to better understand the elucidation of the pathogenic mechanism.

Tyrophagus putrescentiae (Tp) as a storage mite inhabitats in stored grains, hay, and straw at agricultural areas. T. putrescentiae stimulates an immune response and triggers inflammatory cytokines release, and thus it is a source of allergen that sensitize and induce allergic reactions. Also, T. putrescentiae has been reported to cause asthma and atopic disease by cross-reactivity with Dermatophagoides pteronyssinus (Dp). The study on T. putrescentiae in human monocytic THP-1 cells is not enough to understand cytokine expression and pathological mechanisms. The aim of this study is to investigate the effect of T. putrescentiae extract (TpE) on production of inflammatory cytokines and expression of mRNA level in THP-1 cells. THP-1 cells are treated with TpE and supernatants were analyzed for the production of cytokines using enzyme-linked immunosorbent assay (ELISA). mRNA level in the culture cells was measured by a reverse transcriptase-polymerase chain reaction (RT-PCR). As a result of this study, TpE significantly induced secretion of interleukin-6, interleukin-8, and monocyte chemotactic protein-1 (MCP-1) in THP-1 cells in time- and dose-dependent manner. These results suggest that TpE may play a role in contributing to inflammatory disease through stimulation of immune cell. Further research of T. putrescentiae is needed to understand the elucidation of the pathogenic mechanism.