Safety and Immunogenicity of Ad4-HIV Envelope Vaccine Vectors in Healthy Volunteers

Eligibility Criteria

• 1. Age 18 to 49 years for vaccinees. Age 18 to 65 years for household and intimate contacts.
• 2. Negative FDA-approved HIV test.
• 3. Available and willing to participate in follow-up visits and tests for the duration of the study.
• 4. Willing to have samples stored for future research.
• 1. In good general health without clinically significant medical history.
• 2. Assessed as low risk for HIV infection by agreeing to discuss HIV infection risks with the study clinicians, agreeing to HIV risk reduction counseling, and agreeing to avoid behavior associated with high risk of HIV exposure through the last required clinic visit in the protocol schedule.
• 3. Negative beta-HCG pregnancy test for females presumed to be of reproductive potential.
• 4. Female vaccinees and male intimate contacts must meet one of the following criteria:
• * condoms, male or female, with a spermicide.
• * diaphragm or cervical cap with spermicide.
• * contraceptive pills, Norplant, or Depo-Provera (and is not on any medications that would interfere with the effectiveness of these contraceptive agents).
• * male partner has previously undergone a vasectomy for which there is documentation.
• * intrauterine device.
• 5. Male vaccinees and female intimate contacts must agree to consistently practice abstinence or effective birth control (described above) and for 28 days following each vaccination.
• 1. Willing to receive HIV test results and abide by NIH guidelines for partner notification of positive HIV results.
• 2. Physical examination and laboratory results without clinically significant findings within the 8 weeks prior to enrollment.
• 3. Willing to avoid other investigational and/or HIV vaccinations, other than the study agent, from screening through the end-of-study visit.
• 4. Safety laboratory criteria within 8 weeks prior to enrollment:
• * Hematopoietic:
• * White blood cell count and lymphocyte count within 25% of both the lower limit and upper limit of normal for the NIH CC (ranges: 2.985-12.55 K/uL for white blood cells and 0.885 - 4.675 K/uL for lymphocytes).
• * Platelet count of least 150,000/mm\^3.
• * Hemoglobin count within 10% of both the lower limit and upper limit of normal for the NIH CC (ranges: Females 10.08 - 17.27 g/dL, Males 12.33 -19.25 g/dL)
• * Renal: Blood urea nitrogen (BUN) \<23 mg/dL; creatinine within normal limits for the NIH CC (females: 0.51-0.95 mg/dL; males: 0.67-1.17 mg/dL).
• * Hepatic: Serum direct bilirubin within normal limits for the NIH CC (0.0 to 0.3 mg/dL).
• * Metabolic: Alanine aminotransferase (ALT) \< 2 times upper limit of normal range (females: \<66 U/L; males: \<82 U/L).
• * Endocrine: Serum glucose within normal range.
• 5. Additional laboratory criteria:
• * Immunologic: No history of hypogammaglobulinemia.
• * Serologic: Ad4 neutralizing antibody 80% inhibitory dilution \<1:100. (This criterion does not apply to participants in Arm B.)
• 6. Willing to follow precautions for preventing the spread of adenovirus in the community.
• 7. Males must agree not to donate sperm for 28 days following each study vaccination.
• 1. Any condition that, in the investigator s judgement, places the subject at undue risk by participating in the study.
• 1. History of any prior disease or therapy which would affect immune or pulmonary function.
• 2. Prior malignancy, except curatively-treated basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix.
• 3. History of radiation therapy or cytotoxic/cancer chemotherapy.
• 4. History of diabetes mellitus.
• 5. Immunodeficiency or autoimmune disease.
• 6. Acute infection or a recent history (within 6 months) of chronic infection suggestive of immunodeficiency.
• 7. Taking any glucocorticoids or other immunosuppressive medications.
• 8. Asthma is excluded if the participant has ANY of the following:
• 1. Required either oral or parenteral corticosteroids for an exacerbation 2 or more times within the past year, OR
• 2. Needed emergency care, urgent care, hospitalization, or intubation for an acute asthma exacerbation within the past year (eg, would NOT exclude individuals with asthma who meet all other criteria but sought urgent/emergent care solely for asthma medication refills or co-existing conditions unrelated to asthma); OR
• 3. Uses a short-acting rescue inhaler more than 2 days/week for acute asthma symptoms (i.e., not for preventive treatment prior to athletic activity); OR
• 4. Uses medium-to-high-dose inhaled corticosteroids (greater than 250 mcg fluticasone or therapeutic equivalent per day), whether in single-therapy or dual-therapy inhalers (i.e., with a long-acting beta agonist), OR
• 5. Uses more than 1 medication for maintenance therapy daily. Inclusion of anyone on a stable dose of more than 1 medication for maintenance therapy daily for greater than 2 years requires OCRPRO Clinical Safety Office approval.
• 9. Other chronic respiratory disorders including emphysema, interstitial lung disease, pulmonary hypertension, recurrent pneumonia, or recent or ongoing respiratory tract infection. If a respiratory disorder is transient, the study vaccination may be deferred without excluding the participant.
• 10. Female of childbearing potential who is breast-feeding or planning pregnancy during the period from enrollment through 28 days following the last study vaccination.
• 1. Any medical, psychiatric, or social condition, or occupational or other responsibility that, in the judgment of the investigator, would interfere with or serve as a contraindication to receipt of live virus vaccine, protocol adherence, or a participant s ability to give informed consent.
• 2. Psychiatric condition that precludes compliance with the protocol; past or present psychoses; past or present bipolar disorder requiring therapy that has not been well controlled on medication for the past two years; disorder requiring lithium; or suicidal ideation occurring within five years prior to enrollment.
• 3. Individuals that live in the same house or apartment with any of the following will be excluded:
• 1. An individual under 18 years of age.
• 2. An elderly individual (\>65 years of age).
• 3. An immunocompromised or immunosuppressed individual.
• 4. An individual with chronic respiratory disease.
• 5. A woman who is currently pregnant or breastfeeding or planning a pregnancy during the period of vaccination.
• 4. Healthcare worker who has direct contact with immunodeficient, unstable, elderly, or pediatric patients.
• 5. Individuals caring for children \<18 years of age or elderly individuals.
• 6. Receipt of any of the following:
• * Antiviral medications within 30 days prior to vaccination.
• * Blood products within 120 days prior to HIV screening.
• * Immunoglobulin within 60 days prior to HIV screening.
• * Investigational research drugs or any other investigational agent that in the judgement of the Principal Investigator might interact with the study vaccine within 30 days prior to initial study vaccine administration.
• * Allergy treatment with antigen injections within 30 days of study vaccine administration.
• 7. Active hepatitis B or C infection (i.e., hepatitis B or C positive serology with the presence of virus antigen or DNA). Ongoing viral replication will be confirmed by a hepatitis B antigen test or hepatitis C viral load.
• 8. History of Guillain-Barr(SqrRoot)(Copyright) syndrome.
• 9. Indeterminate HIV Western blot test.
• 10. Prior receipt of the Merck Ad5-based HIV vaccine.
• 11. Refusal of any of the individual s intimate contacts to enroll as such on this study.