TY - JOUR
T1 - Impaired gut junctional complexes feature late-treated individuals with suboptimal CD4 + T-cell recovery upon virologically suppressive combination antiretroviral therapy
AU - Tincati, Camilla
AU - Merlini, Esther
AU - Braidotti, Paola
AU - Ancona, Giuseppe
AU - Savi, Federica
AU - Tosi, Delfina
AU - Borghi, Elisa
AU - Callegari, Maria Luisa
AU - Mangiavillano, Benedetto
AU - Barassi, Alessandra
AU - Bulfamante, Gaetano
AU - D'Arminio Monforte, Antonella
AU - Romagnoli, Solange
AU - Chomont, Nicolas
AU - Marchetti, Giulia
PY - 2016
Y1 - 2016
N2 - Objective: HIV-infected individuals with incomplete CD4 + T-cell recovery upon combination antiretroviral therapy (cART) display high levels of immune activation and microbial translocation. However, whether a link exists between gut damage and poor immunological reconstitution remains unknown. Design: Cross-sectional study of the gastrointestinal tract in late cART-treated HIV-infected individuals: 15 immunological nonresponders (CD4 + <350 cells/μl and/or delta CD4 + change from baseline <30%); 15 full responders (CD4 + >350 cells/μl and/or delta CD4 + change from baseline >30%). Methods: We assessed gut structure (junctional complex proteins in ileum and colon) and function (small intestine permeability/damage and microbial translocation parameters). The composition of the fecal microbiome and the size of the HIV reservoir in the gut and peripheral blood were investigated as possible mechanisms underlying mucosal impairment. Results: Markers of intestinal permeability, damage, systemic inflammation, and microbial translocation were comparable in all study individuals, yet the expression of junctional complex proteins in gut biopsies was significantly lower in HIV-infected patients with incomplete CD4 + restoration and negatively correlated with markers of CD4 + reconstitution. Electron microscopy revealed dilated intercellular spaces in individuals lacking immunological response to cART, yet not in patients displaying CD4 + T-cell recovery. Analysis of the fecal microbiome revealed an overall outgrowth of Bacteroides-Prevotella spp. with no differences according to CD4 + T-cell reconstitution. Interestingly, HIV reservoirs in peripheral CD4 + T cells and intestinal tissue negatively correlated with immune recovery. Conclusion: These observations establish gut damage and the size of the HIV reservoir as features of deficient immunological response to cART and provide new elements for interventional strategies in this setting.
AB - Objective: HIV-infected individuals with incomplete CD4 + T-cell recovery upon combination antiretroviral therapy (cART) display high levels of immune activation and microbial translocation. However, whether a link exists between gut damage and poor immunological reconstitution remains unknown. Design: Cross-sectional study of the gastrointestinal tract in late cART-treated HIV-infected individuals: 15 immunological nonresponders (CD4 + <350 cells/μl and/or delta CD4 + change from baseline <30%); 15 full responders (CD4 + >350 cells/μl and/or delta CD4 + change from baseline >30%). Methods: We assessed gut structure (junctional complex proteins in ileum and colon) and function (small intestine permeability/damage and microbial translocation parameters). The composition of the fecal microbiome and the size of the HIV reservoir in the gut and peripheral blood were investigated as possible mechanisms underlying mucosal impairment. Results: Markers of intestinal permeability, damage, systemic inflammation, and microbial translocation were comparable in all study individuals, yet the expression of junctional complex proteins in gut biopsies was significantly lower in HIV-infected patients with incomplete CD4 + restoration and negatively correlated with markers of CD4 + reconstitution. Electron microscopy revealed dilated intercellular spaces in individuals lacking immunological response to cART, yet not in patients displaying CD4 + T-cell recovery. Analysis of the fecal microbiome revealed an overall outgrowth of Bacteroides-Prevotella spp. with no differences according to CD4 + T-cell reconstitution. Interestingly, HIV reservoirs in peripheral CD4 + T cells and intestinal tissue negatively correlated with immune recovery. Conclusion: These observations establish gut damage and the size of the HIV reservoir as features of deficient immunological response to cART and provide new elements for interventional strategies in this setting.
KW - HIV
KW - HIV reservoir
KW - gut junctional complex proteins
KW - immune reconstitution
KW - immunological nonresponders
KW - microbial translocation
KW - HIV
KW - HIV reservoir
KW - gut junctional complex proteins
KW - immune reconstitution
KW - immunological nonresponders
KW - microbial translocation
UR - http://hdl.handle.net/10807/166845
U2 - 10.1097/QAD.0000000000001015
DO - 10.1097/QAD.0000000000001015
M3 - Article
SN - 0269-9370
VL - 30
SP - 991
EP - 1003
JO - AIDS
JF - AIDS
ER -