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Pilot Study of Pyridostigmine Upon Immune Activation in HIV-1 Patients Who Have an Inadequate Immune Response

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Pyridostigmine tablets
Sponsored by
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for HIV Infections focused on measuring AIDS, Immunological non-responders, Neuroimmune modulation, Pyridostigmine, Treatment Experienced

Eligibility Criteria

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

Inclusion Criteria:

  • HIV-1 infected subjects 18 years of age or older
  • Receiving HAART for at least two years
  • At least a viral load determination per year since HAART initiation, all undetectable
  • Patient's status is Immunological Non Responder (InR), that is, his or her viral load is reduced, but CD4+ cell count has not raised accordingly
  • Current viral load: undetectable
  • Patient agrees and signs informed consent

Exclusion Criteria:

  • Concomitant active infectious or neoplastic disease
  • History of new AIDS-defining events during HAART
  • Pregnancy or breast-feeding
  • Patients who have been subjects of an investigational agent, chemotherapy or radiotherapy within the previous 28 days
  • Subjects requiring treatment for Tuberculosis
  • Subjects unable to follow, or comply with the protocol interventions
  • Subjects receiving immunosuppressive treatment, including corticosteroids

Sites / Locations

  • Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
  • Sergio I. Valdés-Ferrer

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

Patients will be taking oral Pyridostigmine 30mg tid, as well as their usual antiretroviral treatment

Outcomes

Primary Outcome Measures

CD4+ Cell Count Change Between Basal and Week 16 of Additive Treatment
Change in total CD4+ T-cell number from baseline to addition of pyridostigmine

Secondary Outcome Measures

Full Information

First Posted
August 17, 2007
Last Updated
October 24, 2019
Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
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1. Study Identification

Unique Protocol Identification Number
NCT00518154
Brief Title
Pilot Study of Pyridostigmine Upon Immune Activation in HIV-1 Patients Who Have an Inadequate Immune Response
Official Title
Pilot Study of an ACh-E Inhibitor Upon Immune Activation Markers in HIV-1 Infected Patients Receiving Highly Active Antiretroviral Therapy (HAART) Showing an Incomplete Immune Response.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether the addition of Pyridostigmine to Highly Active Antiretroviral Therapy (HAART) increases the number of CD4+ T-cells in discordant patients in which viral load diminishes, but T-cell levels remain low after the initiation of treatment.
Detailed Description
In HIV-1 infected patients, HAART suppresses viral replication, reflected by a reduced viral load, and a recovery in the frequency of CD4+ T-cells. The latter is associated with a reduced risk for developing opportunistic infectious diseases, and death. T-cell recovery, however, is highly variable within individuals, suggesting that virological eradication is but one factor of it. A phenomenon known as Immune Discordance has been well known. It reflects a subpopulation -as high as 30% of patients- in whom there is an adequate suppression of viral replication, but CD4+ cell levels rise modestly (below safety levels). In this setting, patients remain susceptible to develop opportunistic infections, have disease progression, and die. Various mechanisms have been proposed, but one common factor is enhanced CD4+-cell activation, leading to cell dysfunction and apoptosis. It is known that an inflammatory response is able to activate the anti-inflammatory cholinergic pathway, in which acetylcholine (ACh) is released and in turn activates nicotinic receptors in macrophages. The result is a diminished synthesis of inflammatory cytokines such as TNF-α, and IL-1. We have recently shown in an ex-vivo, proof-of-concept study carried in HIV-infected subjects in early phases of the infection (not requiring specific treatment) that Pyridostigmine diminishes CD4+-cell activation and an increase in the subpopulation of regulatory T-cells (T-reg). Pyridostigmine, an ACh-esterase inhibitor, has been shown to be safe in other populations, including healthy Gulf War military personnel, and patients with Myasthenia Gravis. Its hypothetical effect is by reducing the degrading rate of the naturally occurring ACh (released by the vagus nerve) by the enzyme ACh-esterase. This in turn enhances its coupling to nicotinic receptors in macrophages that, according to our previous study (unpublished data), improves the T-cell milieu, diminishes T-cell activation (a well known trigger for apoptosis), and enhances T-reg proliferation. The purpose of this study is to determine whether the addition of Pyridostigmine to Highly Active Antiretroviral Therapy (HAART) increases the number of CD4+ T-cells in discordant patients in which viral load diminishes, but T-cell levels remain low after the initiation of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
AIDS, Immunological non-responders, Neuroimmune modulation, Pyridostigmine, Treatment Experienced

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Patients will be taking oral Pyridostigmine 30mg tid, as well as their usual antiretroviral treatment
Intervention Type
Drug
Intervention Name(s)
Pyridostigmine tablets
Other Intervention Name(s)
Mestinon
Intervention Description
Patients will take 30mg tid PO for 12 weeks
Primary Outcome Measure Information:
Title
CD4+ Cell Count Change Between Basal and Week 16 of Additive Treatment
Description
Change in total CD4+ T-cell number from baseline to addition of pyridostigmine
Time Frame
16 weeks after initiation of pyridostigmine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-1 infected subjects 18 years of age or older Receiving HAART for at least two years At least a viral load determination per year since HAART initiation, all undetectable Patient's status is Immunological Non Responder (InR), that is, his or her viral load is reduced, but CD4+ cell count has not raised accordingly Current viral load: undetectable Patient agrees and signs informed consent Exclusion Criteria: Concomitant active infectious or neoplastic disease History of new AIDS-defining events during HAART Pregnancy or breast-feeding Patients who have been subjects of an investigational agent, chemotherapy or radiotherapy within the previous 28 days Subjects requiring treatment for Tuberculosis Subjects unable to follow, or comply with the protocol interventions Subjects receiving immunosuppressive treatment, including corticosteroids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan Sierra-Madero, MD
Organizational Affiliation
Dept. of Infectious Diseases, INNSZ
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jorge Alcocer-Varela, MD
Organizational Affiliation
Dept. of Immunology, INNSZ
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sergio I Valdés-Ferrer, MD, PhD
Organizational Affiliation
Dept. of Neurology, INNSZ
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
City
Tlalpan
State/Province
Ciudad De México
ZIP/Postal Code
14080
Country
Mexico
Facility Name
Sergio I. Valdés-Ferrer
City
Mexico City
State/Province
DF
ZIP/Postal Code
14080
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
29093707
Citation
Valdes-Ferrer SI, Crispin JC, Belaunzaran-Zamudio PF, Rodriguez-Osorio CA, Cacho-Diaz B, Alcocer-Varela J, Cantu-Brito C, Sierra-Madero J. Add-on Pyridostigmine Enhances CD4+ T-Cell Recovery in HIV-1-Infected Immunological Non-Responders: A Proof-of-Concept Study. Front Immunol. 2017 Oct 18;8:1301. doi: 10.3389/fimmu.2017.01301. eCollection 2017.
Results Reference
derived
Links:
URL
http://www.innsz.mx
Description
Institute's web page

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Pilot Study of Pyridostigmine Upon Immune Activation in HIV-1 Patients Who Have an Inadequate Immune Response

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