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Selection of a Protective T Cell-based HIV-1/FIV Vaccine

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University of Florida

Status

Active, not recruiting

Conditions

HIV

Treatments

Other: Non-infected control subjects
Other: HIV positive subjects

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT02389595
IRB201401012-N

Details and patient eligibility

About

The purpose of this research study is to develop a vaccine against Human immunodeficiency virus (HIV), a disease that causes AIDS in people,. The investigator will be looking at viruses similar to HIV in animals. Since these viruses are very similar to HIV, the blood from humans who have been exposed to HIV will be tested to see if the immune system will recognize the HIV and prevent infection.

HIV targets the immune system by attacking certain T cells called CD4+ T cells. There are parts on the AIDS viruses that help the virus infect these cells and other parts that help the immune system prevent viral infection by activating protective T-cells that fight HIV. Different T-cell populations are very important in most vaccines as they act as "effectors" that work as part of the immune system to recognize and fight off HIV infection. When effector T cells are activated by appropriate "protective" part(s) of the virus they either block HIV from reproducing or kill HIV infected cells. By finding these common protective parts of each of these human and animal AIDS viruses, the investigator hopes to make a vaccine that helps the immune system prevent HIV infection by avoiding parts that attack CD4+ T cells and may worsen HIV infection and selecting for parts that stimulate effector T cells that fight HIV infection.

Full description

As a participant in this study a blood drawn will performed.

Enrollment

270 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and female subjects between 18 and 65 years old who are HIV positive

Exclusion criteria

  • Persons with other immune diseases that would result in autoimmunity or aberrant immune responses (such as subjects who have undergone chemotherapy within the past year).

Trial design

270 participants in 2 patient groups

HIV positive subjects
Description:
This group will provide a blood sample.
Treatment:
Other: HIV positive subjects
Non-infected control subjects
Description:
This group consist of de-identified blood samples from a commercial source.
Treatment:
Other: Non-infected control subjects

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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