4.6 Article

Study of the role of CCR5 in a mouse model of intranasal challenge with Yersinia pestis

期刊

MICROBES AND INFECTION
卷 9, 期 9, 页码 1135-1138

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.micinf.2007.04.012

关键词

CCR5; Yersinia pestis; plague; host resistance

资金

  1. NIAID NIH HHS [R21 AI 59689, P30 AI051445, U54 AI 057157, AI 065641, P30 AI 51445, R21 AI065641, R21 AI059689, U54 AI057157] Funding Source: Medline
  2. NIGMS NIH HHS [GM 070977, R01 GM070977-01A1, R37 GM070977, R01 GM070977] Funding Source: Medline

向作者/读者索取更多资源

CCR5 is a chemokine receptor used by HIV-1 to enter cells and has recently been found to act as a pathogen associated molecule pattern receptor. Current positive selection for the high frequency of a CCR5-Delta 32 allele in humans has been attributed to resistance to HIV, smallpox, and plague infections. Using an intranasal mouse model of Y. pestis infection, we have found that lack of CCR5 does not enhance host resistance to Y. pestis infection and that CCR5-mediated responses might have a protective role. CCR5-/- mice exhibited higher levels of circulating RANTES and MIP-l alpha than those exhibited by wild-type mice at the baseline and throughout the course of Y. pesos infection. High levels of RANTES and MIP-l alpha, which are CCR5 ligands that mediate Natural Killer cell migration, may reflect compensation for the absence of CCR5 signaling. (C) 2007 Elsevier Masson SAS. All rights reserved.

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