HIV/AIDS
Conditions
Interventions
None listed
Sponsors
Swedish Institute for Infectious Disease Control
Instituto Nacional de Saude
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age: 18 to 26 years 2. Willing to undergo HIV counseling and testing 3. Have a negative antigen/antibody or antibody ELISA for HIV infection 4. Able to give informed consent 5. Satisfactory completion of an assessment of understanding prior to enrolment defined as 89% correct answers after three opportunities to take the test 6. Basic abilities to read and write 7. Resident in Maputo, and willing to remain so for the duration of the study 8. At low risk of HIV infection, defined as the absence of an identifiable risk factor/ behavior (their presence is therefore an exclusion criteria): sexual partner with HIV sexual partner with unknown HIV serostatus who is also unwilling to use protective condoms consistently in all sexual relations sexual partner is known to be at high risk for HIV more than one sexual partner in the last 6 months history of being an alcoholic [as medically defined or more than 35 units /week] history of STI within past 6 months 9. Verbal assurances that adequate birth control methods are used not to conceive/father a child during the study and up to 3 months after the last vaccine injection. 10. Women shall have a negative urine pregnancy test 11. Be willing to practice safe sex for the duration of the study to avoid sexually transmitted infections including HIV 12. Good health as determined by medical history, physical examination, clinical judgment and by key laboratory parameters as judged by the study physician. 13. Laboratory criteria: Hb >10.5g/dl White blood cell count 1,300/mm3 Lymphocytes >1.000/ mm3 Platelets >120,000/ mm3 Random Blood Glucose < 6.44 mmol/L; if elevated, then a Fasting Blood Glucose < 6.11mmol/L (according to DAIDS Table for Lab Criteria) Bilirubin <1.25 x uln ALT <1.25 x uln Creatinine <1.25 x uln Urine dipstick for protein and blood: negative or trace. (If either is ¿ 1+, complete urinalysis (UA) will be performed.
Exclusion criteria
Exclusion criteria: 1. At risk of HIV infection as mentioned above in the inclusion criteria 2. Active tuberculosis or other systemic infectious process elicited by review of systems, physical examination and laboratory detection 3. A history of immunodeficiency, chronic illness requiring continuous or frequent medical intervention 4. Autoimmune disease by history and physical examination 5. Hives or recurrent hives and severe eczema 6. A history of psychiatric, medical (including traditional medicine) and/or substance abuse problems during the past 6 months that the investigator believes would adversely affect the volunteer's ability to participate in the trial 7. History of epilepsy, or currently taking anti-epileptics 8. Received blood or blood products or immunoglobulins in the past 3 months 9. Receiving immunosuppressive therapy such as systemic corticosteroids or cancer chemotherapy 10. Use of experimental therapeutic agents within 30 days of study entry 11. Reception of any live, attenuated vaccine within 60 days of study entry. 12. Abnormality in ECG that could indicate risk or make interpretation of vaccine effects difficult according to the study operating procedures 13. Previously received an HIV vaccine candidate 14. History of severe local or general reaction to vaccination defined as: Local: Extensive, indurate redness and swelling involving most of the major circumference of the arm, not resolving within 72 hours General: Fever >= 39.5 0C within 48 hours; anaphylaxis; bronchospasm; laryngeal edema; collapse; convulsions or encephalopathy within 72 hours 15. Being a lactating mother 16. Study site employees who are involved in the protocol and may have direct access to the immunogenicity results 17. Unlikely to comply with protocol as judged by the principal investigator or his designate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety;Immunogenicity by IFN-gamma ELISPOT | — |
Secondary
| Measure | Time frame |
|---|---|
| Immunogenicity by intracellular cytokine staining (ICS);Immunogenicity by Lymphoproliferation Assay (LPA) | — |
Countries
Mozambique
Contacts
Public ContactIlesh;Ilesh Jani;Jani
Director of Instituto Nacional de Saude;Director of Instituto Nacional de Saude
Outcome results
None listed