Attenuation of HIV-associated human B cell exhaustion by siRNA downregulation of inhibitory receptors.
Ontology highlight
ABSTRACT: Chronic immune activation in HIV-infected individuals leads to accumulation of exhausted tissue-like memory B cells. Exhausted lymphocytes display increased expression of multiple inhibitory receptors, which may contribute to the inefficiency of HIV-specific antibody responses. Here, we show that downregulation of B cell inhibitory receptors in primary human B cells led to increased tissue-like memory B cell proliferation and responsiveness against HIV. In human B cells, siRNA knockdown of 9 known and putative B cell inhibitory receptors led to enhanced B cell receptor-mediated (BCR-mediated) proliferation of tissue-like memory but not other B cell subpopulations. The strongest effects were observed with the putative inhibitory receptors Fc receptor-like-4 (FCRL4) and sialic acid-binding I
SUBMITTER: Kardava L
PROVIDER: S-EPMC3127436 | biostudies-literature | 2011 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA