Analysis of the Reservoir in Individuals Controlling HIV Infection (ARCH)

Ghent University Hospital (UZ)

Status

Not yet enrolling

Conditions

Hiv

Treatments

Diagnostic Test: HIV Latency Diagnostic Sampling

Study type

Observational

Funder types

Other

Identifiers

NCT06016114

ID 12241 - ARCH

Details and patient eligibility

About

The aim of this study is the gain new insights into HIV latency in HIV controllers through extensive blood an tissue sampling (lymph node, colon biopsies, placenta) from 25 individuals living with HIV and healthy individuals.

Enrollment

25 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Elite Controllers: pVL<50 copies per ml for at least 12 months, treatment naive at the time of inclusion
Viral controllers: pVL <2000 copies/ml; CD4>500/µL for at least two years, treatment naïve at the time of inclusion
Long-term non-progressors: CD4>500/µL, pVL <10000 copies/ml, for at least 7 years, treatment naïve at the time of inclusion
Post treatment controllers: on cART for at least 12 months; pVL <500 copies/ml for at least 2 years after treatment cessation .
PLWH who received bone marrow transplant: people living with HIV who received a bone-marrow transplant for non-HIV related reasons

Exclusion criteria

Current history of opportunistic infection (AIDS defining events as defined in category C of the CDC clinical classification), consisting of chronic HIV-1 infection.
Evidence of active HBV infection (Hepatitis B surface antigen positive or HBV viral load positive in the past and no evidence of subsequent seroconversion (= HBV antigen or viral load negative and positive HBV surface antibody)).
Evidence of active HCV infection (HCV antibody positive result within 60 days prior to study entry with positive HCV viral load or, if the HCV antibody result is negative, a positive HCV RNA result within 60 days prior to study entry).
Current or known history of cardiomyopathy or significant ischemic or cerebrovascular disease.
Current history of cancer.
History of HIV-related thrombocytopenia.
Any condition, including preexisting psychiatric and psychological disorders, which will in the opinion of the investigator interfere with the trial conduct or safety of the participant.
Abnormal results of standard of care laboratory tests:
1. Confirmed haemoglobin <11g/dl for women and <12 g/dl for men
2. Confirmed platelet count <100 000/µl *
3. Confirmed neutrophil count <1000/μl
4. Confirmed AST and/or ALT >10xULN
Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
Acute or serious illness, in the opinion of the site investigator, requiring systemic treatment and/or hospitalization within 60 days prior to entry.
The following treatment will be prohibited three months before screening and during the study:
1. immunosuppressive drugs (inclusive corticosteroids) except for drugs used for topical use.
2. Immunomodulatory drugs including but not limited to Granulocyte-colony stimulating factors, Granulocyte-monocyte colony-stimulating factor, interleukin 2, 7 & 15.