Author/Authors :
Audrain، نويسنده , , Marie and Thomas، نويسنده , , Caroline and Mirallie، نويسنده , , Sophie and Bourgeois، نويسنده , , Nathalie and Sebille، نويسنده , , Véronique and Rabetrano، نويسنده , , Hasina and Durand-Zaleski، نويسنده , , Isabelle and Boisson، نويسنده , , Rachel and Persyn، نويسنده , , Mathieu and Pierres، نويسنده , , Cécile and Mahlaoui، نويسنده , , Nizar and Fischer، نويسنده , , Alain، نويسنده ,
Abstract :
Hepatitis C cirrhosis is associated with a profound disappearance of memory B-cells. We sought to determine if this loss is associated with the expansion of the CD27−CD21− tissue-like memory B-cells with features of B-cell exhaustion. To this end, we quantified the frequency of CD27−CD21− B-cells in healthy, non-cirrhotic HCV-infected, and cirrhotic patients. We examined the expression of putative inhibitory receptors, the proliferative and immunoglobulin-secreting capacity of CD27/CD21-defined B-cell subsets upon B-cell receptor and/or CD40 stimulation. We found that CD27−CD21− B-cells are significantly increased in frequency relative to healthy donors in HCV-infected patients. CD27−CD21− B-cells were hypoproliferative relative to naïve and resting memory B-cells upon agonistic stimulation, but retained similar capacity for antibody secretion. Conclusion: CD27−CD21− tissue-like memory B-cells with exhausted proliferation circulate at increased frequency in cirrhotic and non-cirrhotic HCV-infected patients. This B-cell subset does not appear anergic, exhibiting immunoglobulin-secreting capacity on CD40 agonism indistinguishable from other CD27/CD21-defined B-cell subsets.
Keywords :
Quantification of TRECs , Severe combined immunodeficiency , scid , Neonatal screening