4.7 Article

Duffy antigen receptor for chemokines mediates trans-infection of HIV-1 from red blood cells to target cells and affects HIV-AIDS susceptibility

期刊

CELL HOST & MICROBE
卷 4, 期 1, 页码 52-62

出版社

CELL PRESS
DOI: 10.1016/j.chom.2008.06.002

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资金

  1. Medical Research Council [G8712499] Funding Source: researchfish
  2. MRC [G8712499] Funding Source: UKRI
  3. Medical Research Council [G8712499] Funding Source: Medline
  4. NIAID NIH HHS [R01 AI043279, R37 AI046326-07S1, R01 AI043279-02, R21 AI046326, R01 AI046326-04, R01 AI043279-03, R37 AI046326-09, R01 AI043279-06, R37 AI046326, R37 AI046326-07, HU0001-05-2-0011, R01 AI046326-03, R37 AI046326-08, AI043279, R37 AI046326-06A1, R01 AI043279-06S1, R01 AI043279-07, R01 AI043279-04, R21 AI046326-01, R01 AI046326, R01 AI046326-05, R01 AI043279-08, R01 AI043279-05, R01 AI046326-02, R01 AI046326-01A1] Funding Source: Medline
  5. NIMH NIH HHS [MH069270, R01 MH069270-02, R01 MH069270-01A2, R01 MH069270, R01 MH069270-05, R01 MH069270-03, R01 MH069270-01A2S1, R01 MH069270-04] Funding Source: Medline

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Duffy antigen receptor for chemokines (DARC) expressed on red blood cells (REICs) influences plasma levels of HIV-1-suppressive and proinflammatory chemokines such as CCL5/RANTES. DARC is also the RBC receptor for Plasmodium vivax. Africans with DARC -46C/C genotype, which confers a DARC-negative phenotype, are resistant to vivax malaria. Here, we show that HIV-1 attaches to RBCs via DARC, effecting trans-infection of target cells. In African Americans, DARC -46C/C is associated with 40% increase in the odds of acquiring HIV-1. If extrapolated to Africans, similar to 11% of the HIV-1 burden in Africa may be linked to this genotype. After infection occurs, however, DARC-negative RBC status is associated with slower disease progression. Furthermore, the disease-accelerating effect of a previously described CCL5 polymorphism is evident only in DARC-expressing and not in DARC-negative HIV-infected individuals. Thus, DARC influences HIV/AIDS susceptibility by mediating trans-infection of HIV-1 and by affecting both chemokine-HIV interactions and chemokine-driven inflammation.

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