A Pilot Study to Determine if Raltegravir Eradicates HIV From Peripheral Blood Mononuclear Cells

Inclusion Criteria: * Male or female subjects age 18 or older with HIV-1 infection * CD4 cell counts greater than 200 cells/mm at screening * Plasma HIV RNA \> 1000 copies/mL * Women of childbearing potential must be using an adequate method of contraception to avoid pregnancy throughout the study and for up to eight weeks after the last dose of study drug. Women of childbearing potential includes any woman who has experienced menarche and who has not undergone successful surgical sterilization or who is not post-menopausal. Exclusion Criteria: * Previous exposure to antiretroviral medications used in the treatment of HIV-1 infection * Evidence of genotypic or phenotypic resistance to most of the medications that will be used in the study (tenofovir, emtricitabine, and efavirenz) on a resistance assay obtained through the patient's primary care physicians as a standard of care test * Women with a positive pregnancy test, who are pregnant, or who are breast feeding * Sexually active non-sterilized men not using effective birth control if they have female partners who are of child-bearing potential * Women of child-bearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to eight weeks after the last dose of study drug * Presence of any currently active AIDS-defining category C conditions according to the CDC Classification System for HIV Infection with the exception of stable cutaneous Kaposi's sarcoma * Any active, clinically significant disease that in the opinion of the Principal Investigator may compromise the subject's safety during the trial * Grade 3 or 4 Laboratory abnormalities as defined by a standardized grading scheme based on the DAIDS table - ACTG Toxicity Grading Scale elevations (except pre-existing diabetes mellitus with asymptomatic, non-fasting glucose grade 3 elevations, asymptomatic ≥ grade 3 fasting triglyceride or cholesterol elevations, and subjects with elevated indirect bilirubin) * Active substance abuse or significant psychiatric illness that in the opinion of the Principal Investigator may interfere with study compliance * Prisoners or subjects who are involuntarily incarcerated * Subjects who are compulsorily detained for treatment of either a psychiatric or physical (e.g. infectious disease) illness * Known hypersensitivity to G-CSF