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      Reduced risk of AIDS lymphoma in individuals heterozygous for the CCR5-delta32 mutation.

      Cancer research
      AIDS-Related Opportunistic Infections, epidemiology, genetics, Adult, B-Lymphocytes, drug effects, pathology, Case-Control Studies, Chemokine CCL5, physiology, Cohort Studies, European Continental Ancestry Group, Gene Frequency, Genetic Predisposition to Disease, HIV-1, Humans, Lymphoma, AIDS-Related, Male, Point Mutation, Receptors, CCR5, Risk, Sarcoma, Kaposi, Sequence Deletion, Tetradecanoylphorbol Acetate, pharmacology

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          Abstract

          Non-Hodgkin's lymphoma (NHL) has been increasing in frequency in the industrialized world, but the environmental and genetic factors that contribute to susceptibility are not known. B-cell lymphomas represent a major cause of morbidity and mortality in HIV-infected individuals. The identification of a deletion in the CCR5 chemokine receptor gene that alters the risk for infection and progression to AIDS led us to examine a potential role of this gene in AIDS lymphoma. A matched case-control analysis was performed using all eligible NHL cases in the Multicenter AIDS Cohort Study. Patients were matched for age, study center, time AIDS-free, and slope of the CD4+ T-cell decline. The CCR5-delta32 allele was found to be associated with a 3-fold lower risk of NHL among individuals after controlling for time of infection and progression toward AIDS. The CCR5 gene was not associated with a difference in risk for Kaposi's sarcoma, another common malignancy in AIDS patients, or opportunistic infections. Costimulation of normal phorbol 12-myristate 13-acetate-treated B cells with the CCR5 ligand RANTES induced a proliferative response, indicating that RANTES is a mitogen for B cells. Taken together, these findings suggest that the CCR5 gene plays a role in the risk of NHL in HIV-infected patients, perhaps through a mechanism involving a decreased response of B cells to the mitogenic activity of RANTES.

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