Preventing HIV Infection by Targeting the Immune System Instead of the Virus

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

There are 33.4 million individuals living with HIV/AIDS worldwide. Despite successful HIV prevention strategies such as condom use and reduction of sexual partners, HIV continues to spread at an alarming rate. In 2010, 2.6 millions of new infections were detected. In Sub-Saharan Africa, women represent the two-third of all new infections1. Despite the efforts of the scientific community, there is still no commercial vaccine or microbicide available. To explain this natural protection against HIV, different mechanisms have been identified. These women have a unique immune phenotype that we called Immune Quiescence. This phenotype is characterized by lower expression of genes involved in cellular activation, lower resting levels of inflammatory cytokine production, lower level of systemic activated T cells, increased levels of systemic T regulatory, increased production of anti-viral anti-protease serpins at the female genital tract and reduced numbers of HIV target cells (mainly CD4+ CCR5+ T cells) in the FGT This project aims to induce an Immune Quiescence phenotype (decreasing immune activation) to prevent HIV infection

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: t
View:

• Age greater of 18 years and less than 45

• Be active in sex work for five years or less

• Uterus and cervix present

• Willing to take daily the study drug (acetylsalicylic acid)

• Willing to undergo pelvic exams

• In general good health, no chronic infection and not taking any anti-inflammatory or immunosuppressors

• Being HIV negative

• Without any cardiovascular disease

Locations
Other Locations
Kenya
Kenyan Aids Control Project/University of Nairobi
RECRUITING
Nairobi
Contact Information
Primary
Keith R Fowke, PhD
keith.fowke@umanitoba.ca
204-789-3296
Backup
Julie Lajoie, PhD
julie.lajoie@umanitoba.ca
204-789-3296
Time Frame
Start Date: 2022-01-10
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 300
Treatments
Active_comparator: ASA 325mg
Daily uptake of 325mg ASA
Active_comparator: No drug
no drug
Active_comparator: ASA 81mg
daily uptake of 81mg ASA
Related Therapeutic Areas
Sponsors
Leads: University of Manitoba

This content was sourced from clinicaltrials.gov