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      Induction of inhibitory antibodies to the CCR5 chemokine receptor and their complementary role in preventing SIV infection in macaques.

      European Journal of Immunology
      Animals, Antibodies, Monoclonal, Antibody Formation, CD4-Positive T-Lymphocytes, immunology, Cell Line, Chemotaxis, Leukocyte, Humans, Immunization, Immunoglobulin G, blood, In Vitro Techniques, Macaca mulatta, Receptors, CCR5, genetics, Receptors, HIV, Receptors, Virus, Simian Acquired Immunodeficiency Syndrome, prevention & control, Simian immunodeficiency virus, pathogenicity, physiology, Transfection, Virus Replication

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          Abstract

          The seven-transmembrane G-protein-linked CCR5 molecule functions as a major coreceptor for HIV or simian immunodeficiency virus (SIV) infection. Antibodies to CCR5 were studied in rhesus macaques immunized with SIV grown in human CD4(+) T cells. These macaques were completely protected against i.v. challenge with live SIV. Sera from the protected macaques showed significantly greater inhibition of SIV replication (p < 0.001) and macrophage inflammatory protein-1beta-generated CCR5-dependent chemotaxis (p < 0.01) than sera from unprotected macaques, in the absence of significant neutralizing antibodies to SIV. These two functional assays demonstrate serum antibodies to the CCR5 receptors which were specifically inhibited by CCR5-transfected HEK-293 cells. We postulate that anti-CCR5 antibodies may be complementary to beta-chemokines in blocking CCR5 coreceptors to HIV or SIV binding and fusion of CD4(+) cells.

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