Implication for Strategies of Long Term Control of Viral Replication in Patient With Primary HIV Infection (PHI).

Author(s):  
2007 ◽  
Vol 82 (1) ◽  
pp. 538-545 ◽  
Author(s):  
Sumathi Sankaran ◽  
Michael D. George ◽  
Elizabeth Reay ◽  
Moraima Guadalupe ◽  
Jason Flamm ◽  
...  

ABSTRACT Gut-associated lymphoid tissue (GALT) is an early target for human immunodeficiency virus type 1 (HIV-1) infection and is a site for severe CD4+ T-cell depletion. HIV-associated enteropathy is well-documented in chronic HIV-1 infection. However, the initial host responses to HIV infection in GALT and the early molecular correlates of HIV enteropathogenesis have not been characterized during primary HIV infection. In this study, we provide evidence of viral replication in GALT resident CD4+ T cells and macrophages in primary-stage patients and identify early patterns of host mucosal responses and changes in the molecular microenvironment through gene expression profiling. High levels of viral replication in GALT and marked CD4+ T-cell depletion correlated with decreased expression levels of genes regulating epithelial barrier maintenance and digestive/metabolic functions. These changes coincided with a marked increase in the transcription of immune activation-, inflammation-, and apoptosis-associated genes. Our findings indicate that HIV-induced pathogenesis in GALT emerges at both the molecular and cellular levels prior to seroconversion in primary HIV infection, potentially setting the stage for disease progression by impairing the ability to control viral replication and repair and regenerate intestinal mucosal tissues.


Primary HIV infection (PHI) is usually defined as the first 6 months of infection, from the time of initial infection until viral replication establishes a balance with the immune system. Seroconversion occurs during this time, which may be asymptomatic or present with non-specific viral symptoms, and rarely severe hepatitis or neurological symptoms. This chapter describes the immune responses during this period and clinical features of acute seroconversion illness including common differential diagnoses. Details of how to diagnose PHI and management recommendations are included. There are many benefits to diagnosing PHI, including better prognosis to the patient and reducing onwards transmission.


2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Evguenia Krastinova ◽  
◽  
Remonie Seng ◽  
Jerome Lechenadec ◽  
Henri Panjo ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. e89639 ◽  
Author(s):  
Marlous L. Grijsen ◽  
Ferdinand W. N. M. Wit ◽  
Suzanne Jurriaans ◽  
Frank P. Kroon ◽  
Emile F. Schippers ◽  
...  

2009 ◽  
Vol 49 (6) ◽  
pp. 982-986 ◽  
Author(s):  
Cécile Goujard ◽  
Marie‐Laure Chaix ◽  
Olivier Lambotte ◽  
Christiane Deveau ◽  
Martine Sinet ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-14 ◽  
Author(s):  
Julie C. Gaardbo ◽  
Hans J. Hartling ◽  
Jan Gerstoft ◽  
Susanne D. Nielsen

In the early days of the HIV epidemic, it was observed that a minority of the infected patients did not progress to AIDS or death and maintained stable CD4+ cell counts. As the technique for measuring viral load became available it was evident that some of these nonprogressors in addition to preserved CD4+ cell counts had very low or even undetectable viral replication. They were therefore termed controllers, while those with viral replication were termed long-term nonprogressors (LTNPs). Genetics and virology play a role in nonprogression, but does not provide a full explanation. Therefore, host differences in the immunological response have been proposed. Moreover, the immunological response can be divided into an immune homeostasis resistant to HIV and an immune response leading to viral control. Thus, non-progression in LTNP and controllers may be due to different immunological mechanisms. Understanding the lack of disease progression and the different interactions between HIV and the immune system could ideally teach us how to develop a functional cure for HIV infection. Here we review immunological features of controllers and LTNP, highlighting differences and clinical implications.


Haemophilia ◽  
2001 ◽  
Vol 7 (1) ◽  
pp. 47-52 ◽  
Author(s):  
O. Katsarou ◽  
E. Terpos ◽  
E. Patsouris ◽  
P. Peristeris ◽  
N. Viniou ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document