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The Role of the Gastrointestinal-associated Lymphoid Tissue in the Cure of HIV Infection

Primary Purpose

HIV Infection

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Colonoscopy
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for HIV Infection

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Provision of signed and dated informed consent form Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study Males and females; Age 18-75 Chronic HIV-1 infection, documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to study entry and confirmed by a licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 antigen, plasma HIV-1 RNA viral load Receiving treatment with a molecule with the potential for HIV cure Willingness and ability to undergo colonoscopy twice during the study timeframe Exclusion Criteria: Known coagulopathy or altered coagulation studies Concomitant pregnancy of plans for pregnancy during the study period Concomitant Inflammatory Bowel Disease, Diarrheal disease or other gastrointestinal disease that might alter the intestinal mucosal tissue Concomitant sexually transmitted infection Any other condition which in the opinion of investigators would impede competence, compliance or possibly hinder completion of the study

Sites / Locations

  • Icahn School of Medicine at Mount SinaiRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Patients with HIV Therapy

Arm Description

Subjects receiving therapies with the potential for HIV cure

Outcomes

Primary Outcome Measures

Change in HIV tissue viral load
Change in HIV in tissue-associated HIV RNA viral load at the end of the study at month one compared to baseline

Secondary Outcome Measures

Change in number of Cytotoxic T cells
Change in number of tissue-associated cytotoxic T cells at the end of the study (at month one) period compared to baseline
Change in number of NK Cells
Change in number of tissue-associated NK cells at the end of the study (at month one) period compared to baseline

Full Information

First Posted
December 7, 2022
Last Updated
April 4, 2023
Sponsor
Icahn School of Medicine at Mount Sinai
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1. Study Identification

Unique Protocol Identification Number
NCT05652088
Brief Title
The Role of the Gastrointestinal-associated Lymphoid Tissue in the Cure of HIV Infection
Official Title
The Role of the Gastrointestinal-associated Lymphoid Tissue in the Cure of HIV Infection
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 14, 2023 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to understand the effects of HIV cure strategies on the virus and immune cells that reside within the gastrointestinal tract. Subjects receiving therapies with the potential for HIV cure will undergo a colonoscopy to obtain gastrointestinal tissue for research assays. This study will test whether receiving these therapies will induce changes in the immune cells in the gastrointestinal tract and reduce the tissue-associated HIV viral levels.
Detailed Description
After almost forty years from its first discovery, Human Immunodeficiency Virus (HIV) infection remains uncurable. The major obstacle to a cure for HIV infection is the integration of HIV into the host genome and its persistence in populations of long-lived immune cells subsets. These long-lived resting cells represent a reservoir of transcriptionally silent HIV and they are mostly localized in the secondary lymphoid tissue and the gastrointestinal associated lymphoid tissue (GALT). The most promising HIV cure strategies relay on molecules which can induce enhanced immune responses through antibody mediated effects such as antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis (ADCP) as well as enhanced CD8+ T cells activity. The specific purpose of this study is to evaluate whether the proposed treatment strategies for HIV cure, can induce changes in the gastrointestinal associated immune system (GALT) effector immune cells such as NK cells, cytotoxic CD8+ T Cells and whether treatment with these molecules leads to changes in the amount of tissue-associated HIV virus within the GALT. The results from the proposed study will inform on the ability of these molecules to exert their effect on this critical site of HIV latency and persistence and thus advance the field on their HIV cure potential. Subjects receiving treatment with the potential for HIV cure will undergo a colonoscopy to obtain gastrointestinal tissue for research assays. The research proposal will test the hypothesis of whether these molecules are able to induce changes in the immune cells in the gastrointestinal tract and reduce the tissue-associated HIV viral levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All subjects receiving therapies with the potential for HIV cure who agree to participate in this study, will undergo a colonoscopy to obtain tissue samples for research assays before and after receiving such treatment.
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with HIV Therapy
Arm Type
Experimental
Arm Description
Subjects receiving therapies with the potential for HIV cure
Intervention Type
Procedure
Intervention Name(s)
Colonoscopy
Intervention Description
Colonoscopy is a procedure where an instrument called colonoscope is inserted through the rectum to look at the entire internal surface of the intestine. Participants will be placed on a stretcher on the left side. A colonoscope will be advanced into the colon and into the terminal ileum. The entire procedure should take approximately 40 minutes
Primary Outcome Measure Information:
Title
Change in HIV tissue viral load
Description
Change in HIV in tissue-associated HIV RNA viral load at the end of the study at month one compared to baseline
Time Frame
End of the study (at month one) compared to baseline
Secondary Outcome Measure Information:
Title
Change in number of Cytotoxic T cells
Description
Change in number of tissue-associated cytotoxic T cells at the end of the study (at month one) period compared to baseline
Time Frame
End of the study (at month one) compared to baseline
Title
Change in number of NK Cells
Description
Change in number of tissue-associated NK cells at the end of the study (at month one) period compared to baseline
Time Frame
End of the study (at month one) compared to baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provision of signed and dated informed consent form Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study Males and females; Age 18-75 Chronic HIV-1 infection, documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to study entry and confirmed by a licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 antigen, plasma HIV-1 RNA viral load Receiving treatment with a molecule with the potential for HIV cure Willingness and ability to undergo colonoscopy twice during the study timeframe Exclusion Criteria: Known coagulopathy or altered coagulation studies Concomitant pregnancy of plans for pregnancy during the study period Concomitant Inflammatory Bowel Disease, Diarrheal disease or other gastrointestinal disease that might alter the intestinal mucosal tissue Concomitant sexually transmitted infection Any other condition which in the opinion of investigators would impede competence, compliance or possibly hinder completion of the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Francesca Cossarini, MD
Phone
212-659-9269
Email
francesca.cossarini@mountsinai.org
First Name & Middle Initial & Last Name or Official Title & Degree
Saurabh Mehandru, MD
Phone
212-659-9206
Email
saurabh.mehandru@mssm.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesca Cossarini, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francesca Cossarini, MD
Phone
212-659-9269
Email
francesca.cossarini@mountsinai.org
First Name & Middle Initial & Last Name & Degree
Saurabh Mehandru, MD
Phone
212-659-9206
Email
Saurabh.mehandru@mssm.edu
First Name & Middle Initial & Last Name & Degree
Francesca Cossarini

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share IPD at this time.

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The Role of the Gastrointestinal-associated Lymphoid Tissue in the Cure of HIV Infection

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